References
- Petrov, K. A.; Chauzov, V. A.; Erokhina, T. S. Aminoalkyl Organophosphorus Compounds. Russ. Chem. Rev. 1974, 43, 984–1006. DOI: https://doi.org/10.1070/RC1974v043n11ABEH001877.
- Heaney, F. Functions Containing a Nitrogen and Another Group 15 Element. In Comprehensive Organic Functional Group Transformations; Katritzky, A. R., Meth-Cohn, O., Rees, C. W., Eds.; Pergamon, 1995; Vol. 4, pp. 451–504 DOI: https://doi.org/10.1016/B0-08-044705-8/00255-7.
- Gopalakrishnan, J. Aminophosphines: Their Chemistry and Role as Ligands and Synthons. Appl. Organometal. Chem. 2009, 23, 291–318. DOI: https://doi.org/10.1002/aoc.1515.
- Karasik, A. A.; Balueva, A. S.; Sinyashin, O. G. An Effective Strategy of P,N-Containing Macrocycle Design. C. R. Chim. 2010, 13, 1151–1167. DOI: https://doi.org/10.1016/j.crci.2010.04.006.
- Kollár, L.; Keglevich, G. P-Heterocycles as Ligands in Homogeneous Catalytic Reactions. Chem. Rev. 2010, 110, 4257–4302. DOI: https://doi.org/10.1021/cr900364c.
- Stepanova, V. A.; Smoliakova, I. P. Synthesis of Aminophosphines and Their Applications in Catalysis. Curr. Org. Chem. 2012, 16, 2893–2920. DOI: https://doi.org/10.2174/138527212804546723.
- Karasik, A. A.; Balueva, A. S.; Musina, E. I.; Sinyashin, O. G. Chelating Cyclic Aminomethylphosphines and Their Transition Metal Complexes as a Promising Basis of Bioinspired Mimetic Catalysts. Mendeleev Commun. 2013, 23, 237–248. DOI: https://doi.org/10.1016/j.mencom.2013.09.001.
- Musina, E. I.; Karasik, A. A.; Sinyashin, O. G.; Nikonov, G. N. Heterocyclic Phosphines with P-C-X Fragments (X = O, N, P). Adv. Heterocycl. Chem. 2015, 117, 83–130. DOI: https://doi.org/10.1016/bs.aihch.2015.10.001.
- Li, W.; Zhang, J. Recent Developments in the Synthesis and Utilization of Chiral β-Aminophosphine Derivatives as Catalysts or Ligands. Chem. Soc. Rev. 2016, 45, 1657–1677. DOI: https://doi.org/10.1039/C5CS00469A.
- Bálint, E.; Tajti, Á.; Tripolszky, A.; Keglevich, G. Synthesis of Platinum, Palladium and Rhodium Complexes of α-Aminophosphine Ligands. Dalton Trans. 2018, 47, 4755–4778. DOI: https://doi.org/10.1039/C8DT00178B.
- Mazurkiewicz, R.; Kuźnik, A.; Grymel, M. Październiok-Holewa, A. α-Amino Acid Derivatives with a Cα-P Bond in Organic Synthesis. Arkivoc 2007, VI, 193–216. DOI: https://doi.org/10.3998/ark.5550190.0008.614.
- Mazurkiewicz, R.; Październiok-Holewa, A.; Adamek, J.; Zielińska, K. α-Amidoalkylating Agents: Structure, Synthesis, Reactivity and Application. Adv. Heterocycl. Chem. 2014, 111, 43–94. DOI: https://doi.org/10.1016/B978-0-12-420160-6.00002-1.
- Cherkasov, R. A.; Galkin, V. I. The Kabachnik–Fields Reaction: Synthetic Potential and the Problem of the Mechanism. Russ. Chem. Rev. 1998, 67, 857–882. DOI: https://doi.org/10.1070/RC1998v067n10ABEH000421.
- Keglevich, G.; Bálint, E. The Kabachnik-Fields Reaction: Mechanism and Synthetic Use. Molecules 2012, 17, 12821–12835. DOI: https://doi.org/10.3390/molecules171112821.
- Ali, T. E.; Abdel-Kariem, S. M. Methods for the Synthesis of α-Heterocyclic/Heteroaryl-α-Aminophosphonic Acids and Their Esters. ARKIVOC 2015, VI, 246–287. DOI: https://doi.org/10.3998/ark.5550190.p009.112.
- Zefirov, N. S.; Matveeva, E. D.; Shuvalov, M. V. Third Component Phosphonate (Kabachnik–Fields Reaction). In Science of Synthesis: Multicomponent Reactions; Müller, T. J. J., Ed.; Thieme, 2014; Vol. 1, pp. 273–295. DOI: https://doi.org/10.1055/sos-SD-210-00157.
- Moedritzer, K.; Irani, R. R. The Direct Synthesis of α-Aminomethylphosphonic Acids. Mannich-Type Reactions with Orthophosphorous Acid. J. Org. Chem. 1966, 31, 1603–1607. DOI: https://doi.org/10.1021/jo01343a067.
- Sevrain, C. M.; Berchel, M.; Couthon, H.; Jaffrès, P.-A. Phosphonic Acid: Preparation and Applications. Beilstein J. Org. Chem. 2017, 13, 2186–2213. DOI: https://doi.org/10.3762/bjoc.13.219.
- Merino, P.; Marques-Lopez, E.; Herrera, R. P. Catalytic Enantioselective Hydrophosphonylation of Aldehydes and Imines. Adv. Synth. Catal. 2008, 350, 1195–1208. DOI: https://doi.org/10.1002/adsc.200800131.
- Birum, G. H. Urylenediphosphonates. General Method for the Synthesis of α-Ureidophosphonates and Related Structures. J. Org. Chem. 1974, 39, 209–213. DOI: https://doi.org/10.1021/jo00916a019.
- Oleksyszyn, J.; Subotkowska, L.; Mastalerz, P. Diphenyl 1-Aminoalkanephosphonates. Synthesis 1979, 985–986. DOI: https://doi.org/10.1055/s-1979-28903.
- Oleksyszyn, J.; Gruszecka, E. Amidoalkylation of Phosphorous Acid. Tetrahedron Lett. 1981, 22, 3537–3540. DOI: https://doi.org/10.1016/S0040-4039(01)81951-1.
- Kudzin, M. H.; Kudzin, Z. H.; Drabowicz, J. Thioureidoalkylphosphonates in the Synthesis of 1-Aminoalkylphosphonic Acids. The Ptc-Aminophosphonate Method. ARKIVOC 2011, VI, 227–269. DOI: https://doi.org/10.3998/ark.5550190.0012.617.
- Moiseev, D. V.; James, B. R. Tetrakis(Hydroxymethyl)Phosphonium Salts: Their Properties, Hazards and Toxicities. Phosphorus Sulfur Silicon Relat. Elem. 2020, 195, 263–279. DOI: https://doi.org/10.1080/10426507.2019.1686379.
- Moiseev, D. V.; James, B. R. Syntheses and Rearrangements of Tris(Hydroxymethyl)Phosphine and Tetrakis(Hydroxymethyl) Phosphonium Salts. Phosphorus Sulfur Silicon Relat. Elem. 2020, 195, 687–712. DOI: https://doi.org/10.1080/10426507.2020.1764957.
- Märkl, G.; Jin, G. Y.; Schoerner, C. Chirale Aminomethyl-Phosphine Und Aminomethyl-Diphosphine. Tetrahedron Lett. 1980, 21, 1845–1848. DOI: https://doi.org/10.1016/S0040-4039(00)92795-3.
- Balch, A. L.; Olmstead, M. M.; Rowley, S. P. Preparation and Structural Characterization of Rhodium and Palladium Complexes of Mixed Phosphine/Amine Ligands with Methylene Spacers between Donor Atoms. Inorg. Chim. Acta 1990, 168, 255–264. DOI: https://doi.org/10.1016/S0020-1693(00)80952-4.
- Albright & Wilson Ltd. Substituted Organic Phosphine Derivatives. Br. Patent 854,182, Nov 16, 1960.
- Maier, L.; Organische Phosphorverbindungen, X. Eine Neue Methode zur Knüpfung von P-C-P-Bindungen (Darstellung Von Di-, Tri- und Tetra-tertiären-Phosphinen). Helv. Chim. Acta 1965, 48, 1034–1039. DOI: https://doi.org/10.1002/hlca.19650480507.
- Goodwin, N. J.; Henderson, W.; Sarfo, J. K. FcCH2P(CH2OH)2: A New, Reactive yet Air-Stable Ferrocene-Derived Phosphine [Fc = (η-C5H5)FeC5H4]. Chem. Commun. 1996, 1551–1552. DOI: https://doi.org/10.1039/CC9960001551.
- Goodwin, N. J.; Henderson, W.; Nicholson, B. K.; Sarfo, J. K.; Fawcett, J.; Russell, D. R. Synthesis and Reactivity of the Ferrocene-Derived Phosphine [Fe(η-C5H5){η-C5H4CH2P(CH2OH)2}]. J. Chem. Soc, Dalton Trans. 1997, 4377–4384. DOI: https://doi.org/10.1039/a703666c.
- Ramakrishna, T. V. V.; Elias, A. J.; Vij, A. Synthesis and Reactions of the Ferrocene Derived Hydroxymethyl Phosphine FcCH(CH3)P(CH2OH)2 and Its Sulfide: Crystal Structures of [FcCH(CH3)P(S)R2] R = CH2OH, CH2CH2CN and FcCH(CH3)P(S)(CH2O)2PPh (Fc = Ferrocenyl). J. Organomet. Chem. 2000, 602, 125–132. DOI: https://doi.org/10.1016/S0022-328X(00)00137-6.
- Labios, A.; Heiden, Z. M.; Mock, M. T. Electronic and Steric Influences of Pendant Amine Groups on the Protonation of Molybdenum Bis(Dinitrogen) Complexes. Inorg. Chem. 2015, 54, 4409–4422. DOI: https://doi.org/10.1021/acs.inorgchem.5b00209.
- Issleib, K.; Kümmel, R. Zur Reaktion der Phosphinocarbonsäuren mit Formaldehyd Bzw. N-Hydroxymethyl-Diäthylamin. Z Chem. 2010, 7, 235–235. DOI: https://doi.org/10.1002/zfch.19670070618.
- Sun, J.; Wang, C.; Tan, Z.-W.; Liu, C.-M. A Novel Reactive Phosphonium-Containing Polyelectrolyte with Multiple Reactivities: Monomer Synthesis, RAFT Polymerization and Post-Polymerization Modifications. Polym. Chem. 2020, 11, 4029–4039. DOI: https://doi.org/10.1039/D0PY00362J.
- Kellner, K.; Seidel, B.; Tzschach, A. Organoarsen-Verbindungen: XXXIII. Synthese und Reaktionsverhalten der α-Aminomethylphosphine und -Arsine. J. Organomet. Chem. 1978, 149, 167–176. DOI: https://doi.org/10.1016/S0022-328X(00)94119-6.
- Mironova, Z. N.; Tsvetkov, E. N.; Petrovskaya, L. I.; Negrebetsky, V. V.; Nikolaev, A. V.; Kabachnik, M. I. Syntheses Based on Tetramethylolphosphonium Chloride. Aminomethylphosphines and Their Oxides. Zh. Obshch. Khim. 1972, 42, 2152–2158.
- Mironova, Z. N.; Tsvetkov, E. N.; Nikolaev, A. V.; Kabachnik, M. I. Aminomethylphosphines. U.S.S.R. Patent 247,296, Jul 4, 1969.
- Nikonov, G. N.; Balueva, A. S.; Erastov, O. A.; Arbuzov, B. A. Reactions of Boryloxymethyl- and Hydroxymethylphosphines with Amines. Russ. Chem. Bull. 1989, 38, 1223–1226. DOI: https://doi.org/10.1007/BF00957157.
- Maier, L.; Methylenediphosphine Products and Process for the Preparation Thereof. U.S. Patent 3,253,033, May 24, 1966.
- Maier, L. Organische Phosphorverbindungen XXII. Darstellung und Eigenschaften von Diprimären α,ω-Bis-Phosphino-Alkanen. Helv. Chim. Acta 1966, 49, 842–851. DOI: https://doi.org/10.1002/hlca.19660490203.
- Swor, C. D.; Hanson, K. R.; Zakharov, L. N.; Tyler, D. R. Reactions of Coordinated Hydroxymethylphosphines with NH-Functional Amines: The Phosphorus Lone Pair is Crucial for the Phosphorus Mannich Reaction. Dalton Trans. 2011, 40, 8604–8610. DOI: https://doi.org/10.1039/C1DT10586H.
- Issleib, K.; Leißring, E.; Riemer, M. Aminomethylierung der o-Phenylen-Diphosphine. Z. Chem. 2010, 25, 172–172. DOI: https://doi.org/10.1002/zfch.19850250506.
- Berning, D. E.; Katti, K. V.; Barnes, C. L.; Volkert, W. A. Chemical and Biomedical Motifs of the Reactions of Hydroxymethylphosphines with Amines, Amino Acids, and Model Peptides. J. Am. Chem. Soc. 1999, 121, 1658–1664. DOI: https://doi.org/10.1021/ja9827604.
- Katti, K. V.; Berning, D. E.; Volkert, W. A.; Ketring, A. R.; Churchill, R. Conjugate and Method for Forming Aminomethyl Phosphorus Conjugates. U.S. Patent 5,948,386, Sep 7, 1999.
- Miller, P. W.; Long, N. J.; White, A. J. P. Synthesis, Characterisation and Coordination Chemistry of a New Multidentate P2N4 Ligand System. Dalton Trans. 2009, 5284–5286. DOI: https://doi.org/10.1039/b905749h.
- Chase, D. T.; Moerdyk, J. P.; Bielawski, C. W. Exploring the Chemistry of N,N′-Diamidocarbenes with Organophosphorus Compounds. Org. Lett. 2014, 16, 812–815. DOI: https://doi.org/10.1021/ol4035484.
- Frey, G. D.; Masuda, J. D.; Donnadieu, B.; Bertrand, G. Activation of Si-H, B-H, and P-H Bonds at a Single Nonmetal Center. Angew. Chem. Int. Ed. 2010, 49, 9444–9447. DOI: https://doi.org/10.1002/anie.201005698.
- Becker, G.; Mundt, O. Bildung und Eigenschaften von Acylphosphanen. IX. Reaktion von Phenylbis(Trimethylsilyl) Phosphan mit Formaldehyd und Dimethylformamid. Z. Anorg. Allg. Chem. 1980, 462, 130–142. DOI: https://doi.org/10.1002/zaac.19804620114.
- Märkl, G.; Jin, G. Y. 1.2-Diaza-4-Phospha-Cyclopentane - 1.5-Diaza-3.7-Diphosphabicyclo-[3.3.0]Octane N.N′-[Bisphosphinomethylen]-N.N′-Dimethylhydrazine 1.3-Diaza-5-Phospha-Cyclohexane. Tetrahedron Lett. 1981, 22, 229–232. DOI: https://doi.org/10.1016/0040-4039(81)80062-7.
- Märkl, G.; Jin, G. Y. 1.5-Diaza-3-Phospha-Cycloheptane N,N′-Bis-[Phosphinomethyl]-Ethylendiamine mit Optisch Aktiven Seitenketten. Tetrahedron Lett. 1980, 21, 3467–3470. DOI: https://doi.org/10.1016/S0040-4039(00)78716-8.
- Ignat’eva, S. N.; Balueva, A. S.; Karasik, A. A.; Kulikov, D. V.; Kozlov, A. V.; Latypov, S. K.; Lönnecke, P.; Hey-Hawkins, E.; Sinyashin, O. G. Synthesis of Novel Paracyclophanes with Linear P,N-Containing Spacers. Russ. Chem. Bull. 2007, 56, 1828–1837. DOI: https://doi.org/10.1007/s11172-007-0284-9.
- Kulikov, D. V. Synthesis and Study of the Structure of Cyclophans Containing Aminomethylphosphine Bridges and Their Complexes with Group VIII Transition. Metals. Ph.D. Dissertation, A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan, Russian Federation, 2007.
- Arbuzov, B. A.; Erastov, O. A.; Nikonov, G. N. Synthesis of N,N-Disubstituted 5-Phenyl-1,3,5-Diazaphosphorinanes and Di(Aminomethyl)Phenylphosphines. Izv. Akad. Nauk SSSR, Ser. Khim 1979, 2771–2773.
- Arbuzov, B. A.; Erastov, O. A.; Nikonov, G. N.; Zyablikova, T. A.; Arshinova, R. P.; Kadyrov, R. A. Orientation of Phenyl Group Attached to Phosphorus Atom in 5-Phenyl-1,3-di-R-1,3,5-Diazaphosphorinanes. Russ. Chem. Bull. 1980, 29, 1115–1119. DOI: https://doi.org/10.1007/BF00949165.
- Jain, A.; Helm, M. L.; Linehan, J. C.; DuBois, D. L.; Shaw, W. J. Biologically Inspired Phosphino Platinum Complexes. Inorg. Chem. Commun. 2012, 22, 65–67. DOI: https://doi.org/10.1016/j.inoche.2012.04.039.
- Karasik, A. A.; Georgiev, I. O.; Vasiliev, R. I.; Sinyashin, O. G. Synthesis of Some Novel Water-Soluble Chiral Phosphines. Mendeleev Commun. 1998, 8, 140–141. DOI: https://doi.org/10.1070/MC1998v008n04ABEH000980.
- Kuznetsov, R. M.; Balueva, A. S.; Serova, T. M.; Nikonov, G. N. Synthesis of Aminomethylphosphines with Triazaadamantane Fragments. Russ. J. Gen. Chem. (Engl. Transl.) 2001, 71, 899–902. DOI: https://doi.org/10.1023/A:1012327301121.
- Karasik, A. A.; Georgiev, I. O.; Musina, E. I.; Sinyashin, O. G.; Heinicke, J. Synthesis of Novel Water-Soluble Linear and Heterocyclic Phosphino Amino Acids from 2-Phosphinophenols or 2-Phosphinophenolethers, Formaldehyde and Amino Acids. Polyhedron 2001, 20, 3321–3331. DOI: https://doi.org/10.1016/S0277-5387(01)00950-0.
- Karasik, A. A.; Naumov, R. N.; Sommer, R.; Sinyashin, O. G.; Hey-Hawkins, E. Water-Soluble Aminomethyl(Ferrocenylmethyl) Phosphines and Their Trinuclear Transition Metal Complexes. Polyhedron 2002, 21, 2251–2256. DOI: https://doi.org/10.1016/S0277-5387(02)01168-3.
- Naumov, R. N. Synthesis of New Heterocyclic Di- and Tetraphosphines and Their Complexes with Transition Metals of VII, VIII Groups. Ph.D. Dissertation, A. E. Arbuzov Institute of Organic and Physical Chemistry, Russian Federation, Kazan, 2006.
- Karasik, A. A.; Georgiev, I. O.; Sinyashin, O. G.; Hey-Hawkins, E. Synthesis of Novel Water-Soluble Heterocyclic Phosphino Amino Acids with Bulky Aromatic Substituents on Phosphorus. Polyhedron 2000, 19, 1455–1459. DOI: https://doi.org/10.1016/S0277-5387(00)00400-9.
- Karsch, H. H.; Schreiber, K. A.; Herker, M. A New Route to Sila- and Phosphaheterocycles: Nucleophilic Aminomethylation. Chem. Ber. 1997, 130, 1777–1785. DOI: https://doi.org/10.1002/cber.19971301212.
- Wang, C.; Wang, L.; Zeng, S.; Xu, S.; He, Z. A New BINOL-Derived Chiral Bifunctional Phosphine Organocatalyst: Preparation and Application in Asymmetric (Aza)-Morita-Baylis-Hillman Reactions. Phosphorus Sulfur Silicon Relat. Elem. 2013, 188, 1548–1554. DOI: https://doi.org/10.1080/10426507.2012.761987.
- Baimukhametov, F. Z. Synthesis and Properties of New Primary Phosphines and Aminomethylphosphines with Functionalized Substituents at the Phosphorus Atom. Ph.D. Dissertation, A. E. Arbuzov Institute of Organic and Physical Chemistry, Russian Federation, Kazan, 2002.
- Arbuzov, B. A.; Erastov, O. A.; Nikonov, G. N. Interconversions of Aminomethyl Derivatives of Phenylphosphine. Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 1438–1441.
- Arbuzov, B. A.; Erastov, O. A.; Nikonov, G. N. Interaction of Phosphorus-Containing Phenyl- and Diphenylboronic Acids with Amines. Izv. Akad. Nauk SSSR, Ser. Khim 1980, 952–954.
- Musina, E. I.; Khrizanforova, V. V.; Strelnik, I. D.; Valitov, M. I.; Spiridonova, Y. S.; Krivolapov, D. B.; Litvinov, I. A.; Kadirov, M. K.; Lönnecke, P.; Hey, ‐Hawkins, E.; et al. New Functional Cyclic Aminomethylphosphine Ligands for the Construction of Catalysts for Electrochemical Hydrogen Transformations. Chemistry 2014, 20, 3169–3182. DOI: https://doi.org/10.1002/chem.201304234.
- Karasik, A. A.; Erastov, O. A.; Arbuzov, B. A. Reaction of 1,3,5-Diazaphosphorinanes with Borane. Russ. Chem. Bull. 1989, 38, 1256–1260. DOI: https://doi.org/10.1007/BF00957164.
- Lastra-Calvo, N. Synthesis of Novel Aminomethylphosphine Complexes. Ph.D. Dissertation, Loughborough University, Loughborough, UK, 2014.
- Issleib, K.; Oehme, H.; Kümmel, R.; Leißring, E. 1,3-Azaphospholidine. Chem. Ber. 1968, 101, 3619–3622. DOI: https://doi.org/10.1002/cber.19681011036.
- Palma, E.; Oliveira, B. L.; Figueira, F.; Correia, J. D. G.; Raposinho, P. D.; Santos, I. A Pyrazolylamine-Phosphonate Monoester Chelator for the Fac-[M(CO)3]+ Core (M = Re, 99mTc): Synthesis, Coordination Properties and Biological Assessment. J. Label. Compd. Radiopharm. 2007, 50, 1176–1184. DOI: https://doi.org/10.1002/jlcr.1415.
- Issleib, K.; Khne, U.; Krech, F. Krech, F. 1,5-Aza-Phosphabicyclo[3.2.1]octan—Bildung und Reaktionsverhalten. Z Anorg. Allg. Chem. 1985, 523, 7–13. DOI: https://doi.org/10.1002/zaac.19855230402.
- Niaz, B.; Ghalib, M.; Jones, P. G.; Heinicke, J. W. π-Excess σ2P Ligands: Synthesis of Biaryl-Type 1,3-Benzazaphosphole Hybrid Ligands and Formation of P^P′-M(CO)4 Chelate Complexes. Dalton Trans. 2013, 42, 9523–9532. DOI: https://doi.org/10.1039/c3dt50981h.
- Niaz, B. Synthesis of Novel Biaryl-Type P = C-N-Heterocyclic σ2P,N- and σ2P,σ3P-Hybrid Ligands. Ph.D. Dissertation, University of Greifswald, Greifswald, Germany, 2011.
- Issleib, K.; Vollmer, R. Synthese und Eigenschaften Der 1,3-Benzazaphosphole. Z Anorg. Allg. Chem. 1981, 481, 22–32. DOI: https://doi.org/10.1002/zaac.19814811004.
- Aluri, B. R.; Kindermann, M. K.; Jones, P. G.; Dix, I.; Heinicke, J. Bulky N-Substituted 1,3-Benzazaphospholes: Access via Pd-Catalyzed C-N and C-P Cross Coupling, Lithiation, and Conversion to Novel P = C-PtBu2 Hybrid Ligands. Inorg. Chem. 2008, 47, 6900–6912. DOI: https://doi.org/10.1021/ic800430f.
- Aluri, B. R.; Jones, P. G.; Dix, I.; Heinicke, J. W. π-Excess σ2 P,O Hybrid Ligands: Synthesis of the First 4-Methoxy-1H-1,3-Benzazaphospholes. Synthesis 2014, 46, 1773–1778. DOI: https://doi.org/10.1055/s-0033-1341225.
- Adam, M. S. S.; Jones, P. G.; Heinicke, J. W. Pyrido-Annulated 1,3-Azaphospholes: Synthesis of 1,3-Azaphospholo[5,4-b]Pyridines and Preliminary Reactivity Studies. Eur. J. Inorg. Chem. 2010, 3307–3316. DOI: https://doi.org/10.1002/ejic.201000253.
- Adam, M. S. S.; Kühl, O.; Kindermann, M. K.; Heinicke, J. W.; Jones, P. G. 3-Amino- and 3-Acylamido-2-Phosphonopyridines: Synthesis by Pd-Catalyzed P–C Coupling, Structure and Conversion to Pyrido[b]-Anellated P = C–N Heterocycles. Tetrahedron 2008, 64, 7960–7967. DOI: https://doi.org/10.1016/j.tet.2008.06.010.
- Ghalib, M.; Jones, P. G.; Schulzke, C.; Sziebert, D.; Nyulászi, L.; Heinicke, J. W. π-Rich σ2P-Heterocycles: Bent η1-P- and μ2-P-Coordinated 1,3-Benzazaphosphole Copper(I) Halide Complexes. Inorg. Chem. 2015, 54, 2117–2127. DOI: https://doi.org/10.1021/ic502367d.
- Ghalib, M.; Niaz, B.; Jones, P. G.; Heinicke, J. W. Syntheses of 2-Unsubstituted 1H-1,3-Benzazaphospholes from N-Formyl-2-Bromoanilides. Heteroatom Chem. 2013, 24, 452–456. DOI: https://doi.org/10.1002/hc.21111.
- Ghalib, M.; Jones, P. G.; Lysenko, S.; Heinicke, J. W. Enantiomerically Pure N Chirally Substituted 1,3-Benzazaphospholes: Synthesis, Reactivity toward tBuLi, and Conversion to Functionalized Benzazaphospholes and Catalytically Useful Dihydrobenzazaphospholes. Organometallics 2014, 33, 804–816. DOI: https://doi.org/10.1021/om401184n.
- Heinicke, J.; Tzschach, A. C-Metallierung an Phosphaaromaten-2-Lithio-1-Methyl-1,3-Benzazaphosphol. Tetrahedron Lett. 1982, 23, 3643–3646. DOI: https://doi.org/10.1016/S0040-4039(00)88646-3.
- Bansal, R. K.; Gupta, N.; Heinicke, J.; Nikonov, G. N.; Saguitova, F.; Sharma, D. C. 1H-1,3-Benzazaphospholes: The Organometallic Route and a New Three-Step Synthesis with Reductive Ring Closure. Synthesis 1999, 264–269. DOI: https://doi.org/10.1055/s-1999-3394.
- Ghalib, M.; Lach, J.; Fomina, O. S.; Yakhvarov, D. G.; Jones, P. G.; Heinicke, J. Benzazaphospholine-2-Carboxylic Acids: Synthesis, Structure and Properties of Heterocyclic Phosphanyl Amino Acids. Polyhedron 2014, 77, 10–16. DOI: https://doi.org/10.1016/j.poly.2014.03.046.
- Heinicke, J.; Lach, J.; Basvani, K. R.; Peulecke, N.; Jones, P. G.; Köckerling, M. α-Phosphino Amino Acids: Synthesis, Structure, and Reactivity. Phosphorus Sulfur Silicon Relat. Elem. 2011, 186, 666–677. DOI: https://doi.org/10.1080/10426507.2010.514485.
- Lach, J. α-Phosphanyl-α-Aminosäuren: Synthese, Struktur, Eigenschaften und Reaktivität Unterschiedlich N-Substituierter Phosphanylglycine. Ph.D. Dissertation, University of Greifswald, Greifswald, Germany, 2009.
- Fomina, O. S. New α,α-Phosphinoamino Acids: Synthesis, Structure and Application in Homogeneous Oligomerization Processes of Ethylene. Ph.D. Dissertation, A. E. Arbuzov Institute of Organic and Physical Chemistry, Russian Federation, Kazan, 2017.
- Issleib, K.; Lischewski, M.; Zschunke, A. Aminomethylphosphine. Z. Chem. 2010, 14, 243–244. DOI: https://doi.org/10.1002/zfch.19740140618.
- Bange, C. A.; Ghebreab, M. B.; Ficks, A.; Mucha, N. T.; Higham, L.; Waterman, R. Zirconium-Catalyzed Intermolecular Hydrophosphination Using a Chiral, Air-Stable Primary Phosphine. Dalton Trans. 2016, 45, 1863–1867. DOI: https://doi.org/10.1039/C5DT03544A.
- Romanov, G. V.; Ryzhikova, T. Y.; Pudovik, A. N. Reactions of Organic Hydridophosphines with Azomethines and N-Phenylbenzimidoyl Chloride. Zh. Obshch. Khim. 1990, 60, 1718–1722.
- Sowa, S.; Pietrusiewicz, K. M. Chemoselective Reduction of the P = O Bond in the Presence of P–O and P–N Bonds in Phosphonate and Phosphinate Derivatives. Eur. J. Org. Chem. 2019, 923–938. DOI: https://doi.org/10.1002/ejoc.201801518.
- Oehme, H.; Issleib, K.; Leißring, E.; Zschunke, A. 1,3,5-Azoxaphosphorinane. Synth. Inorg. Metal-Org. Chem. 1974, 4, 453–460. DOI: https://doi.org/10.1080/00945717408069675.
- Issleib, K.; Schmidt, H.; Leissring, E. Zum Cyclisierungsverhalten von 2-Aminoethylphosphinen. J. Organomet. Chem. 1988, 355, 71–77. DOI: https://doi.org/10.1016/0022-328X(88)89011-9.
- Issleib, K.; Brünner, H.-U.; Oehme, H. Benzazaphospholine. Organometal. Chem. Syn. 1971, 1, 161–168.
- Tharmaraj, P.; Kodimunthiri, D.; Prakash, P.; Sheela, C. D. Catalytic and Biological Activity of Transition Metal Complexes of Salicylaldiminopropylphosphine. J. Coord. Chem. 2009, 62, 2883–2892. DOI: https://doi.org/10.1080/00958970902934740.
- Issleib, K.; Winkelmann, H.; Abicht, H.-P. Tetrahydro-Benzazaphosphorine. Synth. Inorg. Metal-Org. Chem. 1974, 4, 191–203. DOI: https://doi.org/10.1080/00945717408069655.
- Issleib, K.; Winkelmann, H.; Abicht, H.-P. 1.3-Benzazaphosphepine. Z Anorg. Allg. Chem. 1976, 424, 97–102. DOI: https://doi.org/10.1002/zaac.19764240202.
- Aluri, B. R.; Niaz, B.; Kindermann, M. K.; Jones, P. G.; Heinicke, J. P = C-N-Heterocycles: Synthesis of Biaryl-Type 1,3-Benzazaphospholes with ortho-Substituted Phenyl or 2-Heteroaryl Groups. Dalton Trans. 2011, 40, 211–224. DOI: https://doi.org/10.1039/C0DT00881H.
- Ghalib, M.; Niaz, B.; Jones, P. G.; Heinicke, J. W. σ2-P Ligands: Convenient Syntheses of N-Methyl-1,3-Benzazaphospholes. Tetrahedron Lett. 2012, 53, 5012–5014. DOI: https://doi.org/10.1016/j.tetlet.2012.07.037.
- Ghalib, M.; Jones, P. G.; Heinicke, J. W. Solvent-Controlled Lithiation of P = C–N-Heterocycles: Synthesis of Mono- and Bis(Trimethylsilyl)-Tert-Butyl-Dihydrobenzazaphospholes – a New Type of Highly Bulky and Basic Phosphine Ligands. J. Organomet. Chem. 2014, 763-764, 44–51. DOI: https://doi.org/10.1016/j.jorganchem.2014.04.014.
- Niaz, B.; Iftikhar, F.; Kindermann, M. K.; Jones, P. G.; Heinicke, J. Coplanar Tetracyclic π-Excess σ2P Ligands. Eur. J. Inorg. Chem. 2013, 4220–4227. DOI: https://doi.org/10.1002/ejic.201300342.
- Heinicke, J.; Gupta, N.; Surana, A.; Peulecke, N.; Witt, B.; Steinhauser, K.; Bansal, R. K.; Jones, P. G. Synthesis of 1H-1,3-Benzazaphospholes: Substituent Influence and Mechanistical Aspects. Tetrahedron 2001, 57, 9963–9972. DOI: https://doi.org/10.1016/S0040-4020(01)01019-5.
- Aluri, B. R.; Shah, K.; Gupta, N.; Fomina, O. S.; Yakhvarov, D. G.; Ghalib, M.; Jones, P. G.; Schulzke, C.; Heinicke, J. W. σ2P,O-Hybrid Ligands: Synthesis of the First 4-Hydroxy-1,3-Benzazaphospholes by ortho-Lithiation of m-Amidophenyl Diethyl Phosphates. Eur. J. Inorg. Chem. 2014, 5958–5968. DOI: https://doi.org/10.1002/ejic.201402527.
- Huang, H.; Luo, H.; Tao, G.; Cai, W.; Cao, J.; Duan, Z.; Mathey, F. Selective Synthesis of (Z)-Diazadiphosphafulvalene from 2,2'-bis-Azaphosphindole. Org. Lett. 2018, 20, 1027–1030. DOI: https://doi.org/10.1021/acs.orglett.7b03971.
- Ghalib, M. P = C-N-Heterocyclen – Zugang zu und Synthesepotential von Benzazaphospholen für Neuartige σ2- und σ3-P-Übergangsmetallkomplexe und Katalysatoren. Ph.D. Dissertation, University of Greifswald, Greifswald, Germany, 2013.
- Pudovik, A. N.; Romanov, G. V.; Pozhidaev, V. M. α-Aminobenzylphosphines. Synthesis and Some of Their Properties. Zh. Obshch. Khim. 1978, 48, 1008–1013.
- Li, J.; Lamsfus, C. A.; Song, C.; Liu, J.; Fan, G.; Maron, L.; Cui, C. Samarium-Catalyzed Diastereoselective Double Addition of Phenylphosphine to Imines and Mechanistic Studies by DFT Calculations. ChemCatChem 2017, 9, 1368–1372. DOI: https://doi.org/10.1002/cctc.201700003.
- Georgiev, I. O.; Karasik, A. A.; Nigmadzyanov, F. F.; Nikonov, G. N. Metal Complexes of Bis(o-Carboxyphenylaminomethyl) Phosphine. Koord. Khim. 1995, 21, 222–226.
- Karasik, A. A. Cyclic β-Heteroatomic Phosphines in the Coordination Chemistry of Transition Metals. Habilitation Dissertation, A. E. Arbuzov Institute of Organic and Physical Chemistry, Russian Federation, Kazan, 2003.
- Spiridonova, Y. S.; Balueva, A. S.; Krivolapov, D. B.; Litvinov, I. A.; Musina, E. I.; Karasik, A. A.; Sinyashin, O. G. New Aminomethylphosphines with Cyanophenyl Substituents at the Nitrogen Atoms. Russ. Chem. Bull. 2013, 62, 2487–2494. DOI: https://doi.org/10.1007/s11172-013-0360-2.
- Abdur-Rashid, K.; Graham, T.; Tsang, C.-W.; Chen, X.; Guo, R.; Jia, W.; Amoroso, D.; Sui-Seng, C. Method for the Production of Hydrogen from Ammonia Borane. World Patent 2008/141439, Nov 27, 2008.
- Gonschorowsky, M.; Merz, K.; Driess, M. Cyclohexylbis (Hydroxymethyl)Phosphane: A Hydrophilic Phosphane Capable of Forming Novel Hydrogen-Bonding Networks. Eur. J. Inorg. Chem. 2006, 455–463. DOI: https://doi.org/10.1002/ejic.200500823.
- Gonschorowsky, M. Beiträge Zur Chemie Hydrophiler Phosphane. Ph.D. Dissertation, Ruhr-Universität Bochum, Bochum, Germany, 2004.
- Lach, J.; Palm, G. J.; Jones, P. G.; Heinicke, J. W. One-Pot Synthesis of Phosphanylbis(N-Arylglycines) and Spontaneous Diastereoselective Lactamization of P-Alkyl Derivatives to Form Five-Membered P,N-Heterocyclic Amino Acids. Eur. J. Inorg. Chem. 2016, 3417–3422. DOI: https://doi.org/10.1002/ejic.201600202.
- Heinicke, J. W.; Lach, J.; Basvani, K. R.; Ghalib, M.; Fomina, O. S.; Yakhvarov, D. G. Synthesis, Structure and Reactivity of Acyclic and Heterocyclic α-Phosphino Amino Acids. Phosphorus Sulfur Silicon Relat. Elem. 2019, 194, 279–280. DOI: https://doi.org/10.1080/10426507.2018.1521408.
- Musina, E. I.; Kuznetsov, R. M.; Gubanov, E. F.; Balueva, A. S.; Nikonov, G. N. Two Paths for the Synthesis of Poly(Diazadiphosphacyclooctanes). Zh. Obshch. Khim. 1999, 69, 928–933.
- Arbuzov, B. A.; Erastov, O. A.; Nikonov, G. N. Interaction of Esters of Phenyl- and Diphenyl-Boronic Acids and Bis(Hydroxymethyl)Phenylphosphine with One Mole of Aniline. Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2129–2131.
- Moiseev, D. V.; James, B. R.; Gushchin, A. V. NMR Spectroscopic Studies on the 1:1 Interaction of Tris(Hydroxymethyl)Phosphine with Cinnamic Acids. Eur. J. Inorg. Chem. 2014, 6275–6280. DOI: https://doi.org/10.1002/ejic.201402889.
- Lim, D. W.; Nettles, D. L.; Setton, L. A.; Chilkoti, A. Rapid Cross-Linking of Elastin-like Polypeptides with (Hydroxymethyl) Phosphines in Aqueous Solution. Biomacromolecules 2007, 8, 1463–1470. DOI: https://doi.org/10.1021/bm061059m.
- Nettles, D. L.; Haider, M. A.; Chilkoti, A.; Setton, L. A. Neural Network Analysis Identifies Scaffold Properties Necessary for in Vitro Chondrogenesis in Elastin-like Polypeptide Biopolymer Scaffolds. Tissue Eng., A 2010, 16, 11–20. DOI: https://doi.org/10.1089/ten.tea.2009.0134.
- Chung, C.; Anderson, E.; Pera, R. R.; Pruitt, B. L.; Heilshorn, S. C. Hydrogel Crosslinking Density Regulates Temporal Contractility of Human Embryonic Stem Cell-Derived Cardiomyocytes in 3D Cultures. Soft Matter. 2012, 8, 10141–10148. DOI: https://doi.org/10.1039/C2SM26082D.
- Nettles, D. L.; Kitaoka, K.; Hanson, N. A.; Flahiff, C. M.; Mata, B. A.; Hsu, E. W.; Chilkoti, A.; Setton, L. A. In Situ Crosslinking Elastin-Like Polypeptide Gels for Application to Articular Cartilage Repair in a Goat Osteochondral Defect Model. Tissue Eng., A 2008, 14, 1133–1140. DOI: https://doi.org/10.1089/ten.tea.2007.0245.
- Nettles, D. L.; Chilkoti, A.; Setton, L. A. Early Metabolite Levels Predict Long-Term Matrix Accumulation for Chondrocytes in Elastin-Like Polypeptide Biopolymer Scaffolds. Tissue Eng., A 2009, 15, 2113–2121. DOI: https://doi.org/10.1089/ten.tea.2008.0448.
- Li, L.; Teller, S.; Clifton, R. J.; Jia, X.; Kiick, K. L. Tunable Mechanical Stability and Deformation Response of a Resilin-Based Elastomer. Biomacromolecules 2011, 12, 2302–2310. DOI: https://doi.org/10.1021/bm200373p.
- Charati, M. B.; Ifkovits, J. L.; Burdick, J. A.; Linhardt, J. G.; Kiick, K. L. Hydrophilic Elastomeric Biomaterials Based on Resilin-Like Polypeptides. Soft Matter. 2009, 5, 3412–3416. DOI: https://doi.org/10.1039/b910980c.
- Lim, D. W.; Nettles, D. L.; Setton, L. A.; Chilkoti, A. In Situ Cross-Linking of Elastin-like Polypeptide Block Copolymers for Tissue Repair. Biomacromolecules 2008, 9, 222–230. DOI: https://doi.org/10.1021/bm7007982.
- Lim, D. W. In-Situ Crosslinkable and Self-Assembling Elastin-like Polypeptide Block Copolymers for Cartilage Tissue Repair. Ph.D. Dissertation, Duke University, Durham, North Carolina, 2007.
- Gali, H.; Prabhu, K. R.; Karra, S. R.; Katti, K. V. Facile Ring-Opening Reactions of Phthalimides as a New Strategy to Synthesize Amide-Functionalized Phosphonates, Primary Phosphines, and Bisphosphines. J. Org. Chem. 2000, 65, 676–680. DOI: https://doi.org/10.1021/jo991067b.
- Schenk, C. Etude Sur la Réactivité du THP (Tris(Hydroxyméthyl)Phosphine) et Développement de Composés Potentiellement Efficaces en Tant Que Retardants de Flamme. Ph.D. Dissertation, Université de Neuchâtel, Neuchâtel, Switzerland, 2014.
- Lake, A. J. Advances in Polyaromatic and Ferrocenyl Phosphine Chemistry. Ph.D. Dissertation, Loughborough University, Loughborough, UK, 2010.
- Gali, H.; Karra, S. R.; Reddy, V. S.; Katti, K. V. Design and Development of the First Peptide-Chelating Bisphosphane Bioconjugate from a Novel Functionalized Phosphorus(III) Hydride Synthon. Angew. Chem. Int. Ed. 1999, 38, 2020–2023. DOI: https://doi.org/10.1002/(SICI)1521-3773(19990712)38:13/14 < 2020::AID-ANIE2020 > 3.0.CO;2-R.
- Bunton, C. A.; Huang, S. K. Reactions of the Tri-p-Anisylmethyl Cation with Primary and Secondary Amines. J. Am. Chem. Soc. 1974, 96, 515–522. DOI: https://doi.org/10.1021/ja00809a029.
- Heo, C. K. M.; Bunting, J. W. Nucleophilicity towards a Vinylic Carbon Atom: Rate Constants for the Addition of Amines to the 1-Methyl-4-Vinylpyridinium Cation in Aqueous Solution. J. Chem. Soc., Perkin Trans. 1994, 2, 2279–2290. DOI: https://doi.org/10.1039/P29940002279.
- Brotzel, F.; Chu, Y. C.; Mayr, H. Nucleophilicities of Primary and Secondary Amines in Water. J. Org. Chem. 2007, 72, 3679–3688. DOI: https://doi.org/10.1021/jo062586z.
- Landis, C. R.; Jin, W.; Owen, J. S.; Clark, T. P. Rapid Access to Diverse Arrays of Chiral 3,4-Diazaphospholanes. Angew. Chem. Int. Ed. 2001, 40, 3432–3434. DOI: https://doi.org/10.1002/1521-3773(20010917)40:18 < 3432::AID-ANIE3432 > 3.0.CO;2-3.
- Landis, C. R.; Jin, W.; Owen, J. S.; Clark, T. P. Diazaphosphacycles. World Patent 03/010174, Feb 6., 2003.
- Clark, T. P. Synthesis of 3,4-Diazaphospholanes and Their Application to Asymmetric Catalysis. Ph.D. Dissertation, the University of Wisconsin-Madison, Madison, U.S., 2004.
- Hashiguch, B. G. Synthesis and Development of Bidentate 3,4-Diazaphospholanes for Metal-Catalyzed Reactions. Ph.D. Dissertation, the University of Wisconsin-Madison, Madison, U.S., 2008.
- Landis, C. R.; Nelson, R. C.; Jin, W.; Bowman, A. C. Synthesis, Characterization, and Transition-Metal Complexes of 3,4-Diazaphospholanes. Organometallics 2006, 25, 1377–1391. DOI: https://doi.org/10.1021/om050922g.
- Nelson, R. C. 3,4-Diazaphospholane Ligands: Syntheses, Properties, and Applications to Catalysis. Ph.D. Dissertation, the University of Wisconsin-Madison, Madison, U.S., 2006.
- Clark, T. P.; Landis, C. R.; Freed, S. L.; Klosin, J.; Abboud, K. A. Highly Active, Regioselective, and Enantioselective Hydroformylation with Rh Catalysts Ligated by Bis-3,4-Diazaphospholanes. J. Am. Chem. Soc. 2005, 127, 5040–5042. DOI: https://doi.org/10.1021/ja050148o.
- Nelsen, E. R.; Landis, C. R. Interception and Characterization of Alkyl and Acyl Complexes in Rhodium-Catalyzed Hydroformylation of Styrene. J. Am. Chem. Soc. 2013, 135, 9636–9639. DOI: https://doi.org/10.1021/ja404799m.
- Jones, B. R.; Abrams, M. L.; Landis, C. R.; May, S. A.; Campbell, A. N.; Martinelli, J. R.; Calvin, J. R. Scalable Synthesis of Enantiopure Bis-3,4-Diazaphospholane Ligands for Asymmetric Catalysis. J. Org. Chem. 2016, 81, 11965–11970. DOI: https://doi.org/10.1021/acs.joc.6b01915.
- Wildt, J.; Brezny, A. C.; Landis, C. R. Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes. Organometallics 2017, 36, 3142–3151. DOI: https://doi.org/10.1021/acs.organomet.7b00475.
- Adint, T. Improving Accessibility of Asymmetric Hydroformylation through Ligand Libraries and Immobilization. Ph.D. Dissertation, the University of Wisconsin-Madison, Madison, U.S., 2014.
- Clark, T. P.; Landis, C. R. Resolved Chiral 3,4-Diazaphospholanes and Their Application to Catalytic Asymmetric Allylic Alkylation. J. Am. Chem. Soc. 2003, 125, 11792–11793. DOI: https://doi.org/10.1021/ja036359f.
- Adint, T. T.; Wong, G. W.; Landis, C. R. Libraries of Bisdiazaphospholanes and Optimization of Rhodium-Catalyzed Enantioselective Hydroformylation. J. Org. Chem. 2013, 78, 4231–4238. DOI: https://doi.org/10.1021/jo400525w.
- Landis, C. R.; Clark, T. P. Solid-Phase Synthesis of Chiral 3,4-Diazaphospholanes and Their Application to Catalytic Asymmetric Allylic Alkylation. PNAS 2004, 101, 5428–5432. DOI: https://doi.org/10.1073/pnas.0307572100.
- Watkins, A. L.; Hashiguchi, B. G.; Landis, C. R. Highly Enantioselective Hydroformylation of Aryl Alkenes with Diazaphospholane Ligands. Org. Lett. 2008, 10, 4553–4556. DOI: https://doi.org/10.1021/ol801723a.
- Watkins, A. L.; Landis, C. R. Regioselective Rhodium-Catalyzed Hydroformylation of 1,3-Dienes to Highly Enantioenriched β,γ-Unsaturated Aldehyes with Diazaphospholane Ligands. Org. Lett. 2011, 13, 164–167. DOI: https://doi.org/10.1021/ol102797t.
- Nelsen, E. R.; Brezny, A. C.; Landis, C. R. Interception and Characterization of Catalyst Species in Rhodium Bis(Diazaphospholane)-Catalyzed Hydroformylation of Octene, Vinyl Acetate, Allyl Cyanide, and 1-Phenyl-1,3-Butadiene. J. Am. Chem. Soc. 2015, 137, 14208–14219. DOI: https://doi.org/10.1021/jacs.5b09858.
- Klosin, J.; Landis, C. R. Ligands for Practical Rhodium-Catalyzed Asymmetric Hydroformylation. Acc. Chem. Res. 2007, 40, 1251–1259. DOI: https://doi.org/10.1021/ar7001039.
- Brezny, A. C.; Landis, C. R. Recent Developments in the Scope, Practicality, and Mechanistic Understanding of Enantioselective Hydroformylation. Acc. Chem. Res. 2018, 51, 2344–2354. DOI: https://doi.org/10.1021/acs.accounts.8b00335.
- Arbuzov, B. A.; Erastov, O. A.; Romanova, I. P.; Efremov, Y. Y.; Musin, R. Z. Reaction of Dihydroxymethylphenylphosphine with o-Phenylenediamine. Russ. Chem. Bull. 1982, 31, 399–401. DOI: https://doi.org/10.1007/BF00948268.
- Arbuzov, B. A.; Erastov, O. A.; Nikonov, G. N.; Arshinova, R. P.; Romanova, I. P.; Kadyrov, R. A. Synthesis and Structure of 1,5-Diaza-3,7-Diphosphacyclooctanes. Russ. Chem. Bull. 1983, 32, 1672–1676. DOI: https://doi.org/10.1007/BF00954289.
- Kane, J. C.; Wong, E. H.; Yap, G. P. A.; Rheingold, A. L. Synthesis and Structural Studies of Molybdenum and Palladium Complexes of 1,5-Diaza-3,7-Diphosphacyclooctane Ligands. Polyhedron 1999, 18, 1183–1188. DOI: https://doi.org/10.1016/S0277-5387(98)00413-6.
- Märkl, G.; Jin, G. Y.; Schoerner, C. 1. 5-Diaza-3,7-Diphospha-Cyclooctane. Tetrahedron Lett. 1980, 21, 1409–1412. DOI: https://doi.org/10.1016/S0040-4039(00)92732-1.
- Stubbs, J. M.; Chapple, D. E.; Boyle, P. D.; Blacquiere, J. M. Catalyst Pendent-Base Effects on Cyclization of Alkynyl Amines. ChemCatChem 2018, 10, 4001–4009. DOI: https://doi.org/10.1002/cctc.201800713.
- Hoffert, W. A.; Roberts, J. A. S.; Bullock, R. M.; Helm, M. L. Production of H2 at Fast Rates Using a Nickel Electrocatalyst in water-acetonitrile solutions. Chem. Commun. 2013, 49, 7767–7769. DOI: https://doi.org/10.1039/C3CC43203C.
- Kilgore, U. J.; Roberts, J. A. S.; Pool, D. H.; Appel, A. M.; Stewart, M. P.; DuBois, M. R.; Dougherty, W. G.; Kassel, W. S.; Bullock, R. M.; DuBois, D. L. [Ni(PPh2NC6H4X2)2]2+ Complexes as Electrocatalysts for H2 Production: Effect of Substituents, Acids, and Water on Catalytic Rates. J. Am. Chem. Soc. 2011, 133, 5861–5872. DOI: https://doi.org/10.1021/ja109755f.
- Galan, B. R.; Schöffel, J.; Linehan, J. C.; Seu, C.; Appel, A. M.; Roberts, J. A. S.; Helm, M. L.; Kilgore, U. J.; Yang, J. Y.; DuBois, D. L.; Kubiak, C. P. Electrocatalytic Oxidation of Formate by [Ni(PR2NR′2)2(CH3CN)]2+ Complexes. J. Am. Chem. Soc. 2011, 133, 12767–12779. DOI: https://doi.org/10.1021/ja204489e.
- Das, A. K.; Engelhard, M. H.; Lense, S.; Roberts, J. A. S.; Bullock, R. M. Covalent Attachment of Diphosphine Ligands to Glassy Carbon Electrodes via Cu-Catalyzed Alkyne-Azide Cycloaddition. Metallation with Ni(II). Dalton Trans. 2015, 44, 12225–12233. DOI: https://doi.org/10.1039/C5DT00162E.
- Bergamini, G.; Natali, M. Homogeneous vs. Heterogeneous Catalysis for Hydrogen Evolution by a Nickel(II) Bis(Diphosphine) Complex. Dalton Trans. 2019, 48, 14653–14661. DOI: https://doi.org/10.1039/C9DT02846C.
- Goff, A.; Artero, V.; Jousselme, B.; Tran, P. D.; Guillet, N.; Métayé, R.; Fihri, A.; Palacin, S.; Fontecave, M. From Hydrogenases to Noble Metal–Free Catalytic Nanomaterials for H2 Production and Uptake. Science 2009, 326, 1384–1387. DOI: https://doi.org/10.1126/science.1179773.
- Jain, A.; Lense, S.; Linehan, J. C.; Raugei, S.; Cho, H.; DuBois, D. L.; Shaw, W. J. Incorporating Peptides in the Outer-Coordination Sphere of Bioinspired Electrocatalysts for Hydrogen Production. Inorg. Chem. 2011, 50, 4073–4085. DOI: https://doi.org/10.1021/ic1025872.
- Pool, D. H.; Stewart, M. P.; O'Hagan, M.; Shaw, W. J.; Roberts, J. A. S.; Bullock, R. M.; DuBois, D. L. Acidic Ionic Liquid/Water Solution as Both Medium and Proton Source for Electrocatalytic H2 Evolution by [Ni(P2N2)2]2+ Complexes. PNAS 2012, 109, 15634–15639. DOI: https://doi.org/10.1073/pnas.1120208109.
- Cardenas, A. J. P.; Ginovska, B.; Kumar, N.; Hou, J.; Raugei, S.; Helm, M. L.; Appel, A. M.; Bullock, R. M.; O'Hagan, M. Controlling Proton Delivery through Catalyst Structural Dynamics. Angew. Chem. Int. Ed. 2016, 55, 13509–13513. DOI: https://doi.org/10.1002/anie.201607460.
- Karasik, A. A.; Naumov, R. N.; Balueva, A. S.; Spiridonova, Y. S.; Golodkov, O. N.; Novikova, H. V.; Belov, G. P.; Katsyuba, S. A.; Vandyukova, E. E.; Lönnecke, P.; et al. Synthesis, Structure, and Transition Metal Complexes of Amphiphilic 1,5-Diaza-3,7-Diphosphacyclooctanes. Heteroatom Chem. 2006, 17, 499–513. DOI: https://doi.org/10.1002/hc.20272.
- Zhou, Y.; Yang, S.; Huang, J. Light-Driven Hydrogen Production from Aqueous Solutions Based on a New Dubois-Type Nickel Catalyst. Phys. Chem. Chem. Phys. 2017, 19, 7471–7475. DOI: https://doi.org/10.1039/C7CP00247E.
- Bosch, B.; Rombouts, J. A.; Orru, R. V. A.; Reek, J. N. H.; Detz, R. J. Nickel-Based Dye-Sensitized Photocathode: Towards Proton Reduction Using a Molecular Nickel Catalyst and an Organic Dye. ChemCatChem 2016, 8, 1392–1398. DOI: https://doi.org/10.1002/cctc.201600025.
- Pool, D. H.; DuBois, D. L. [Ni(PPh2NAr2)2(NCMe)][BF4]2 as an Electrocatalyst for H2 Production: PPh2NAr2 = 1,5-(Di(4-(Thiophene-3-yl)Phenyl)-3,7-Diphenyl-1,5-Diaza-3,7-Diphosphacyclooctane). J. Organomet. Chem. 2009, 694, 2858–2865. DOI: https://doi.org/10.1016/j.jorganchem.2009.04.010.
- Reback, M. L.; Ginovska-Pangovska, B.; Ho, M.-H.; Jain, A.; Squier, T. C.; Raugei, S.; Roberts, J. A. S.; Shaw, W. J. The Role of a Dipeptide Outer-Coordination Sphere on H2-Production Catalysts: Influence on Catalytic Rates and Electron Transfer. Chem. Eur. J. 2013, 19, 1928–1941. DOI: https://doi.org/10.1002/chem.201202849.
- Brunner, F. M.; Neville, M. L.; Kubiak, C. P. Investigation of Immobilization Effects on Ni(P2N2)2 Electrocatalysts. Inorg. Chem. 2020, 59, 16872–16881. DOI: https://doi.org/10.1021/acs.inorgchem.0c01669.
- Klug, C. M.; Cardenas, A. J. P.; Bullock, R. M.; O’Hagan, M.; Wiedner, E. S. Reversing the Tradeoff between Rate and Overpotential in Molecular Electrocatalysts for H2 Production. ACS Catal. 2018, 8, 3286–3296. DOI: https://doi.org/10.1021/acscatal.7b04379.
- Karasik, A. A.; Heinicke, J. W.; Balueva, A. S.; Thede, G.; Jones, P. G.; Sinyashin, O. G. Pt- and Pd-Complexes with Acyclic and Heterocyclic P-Hydroxyaryl-Substituted N-Phosphanylmethyl Amino Acids RP(CH2NHR')2 and (RPCH2NR'CH2)2 – Evaluation of (P^O)M Chelate Formation. Eur. J. Inorg. Chem. 2020, 3682–3691. DOI: https://doi.org/10.1002/ejic.202000551.
- Spiridonova, Y. S.; Nikolaeva, Y. A.; Balueva, A. S.; Musina, E. I.; Litvinov, I. A.; Strelnik, I. D.; Khrizanforova, V. V.; Budnikova, Y. G.; Karasik, A. A. Synthesis and Structure of Iron (II) Complexes of Functionalized 1,5-Diaza-3,7-Diphosphacyclooctanes. Molecules 2020, 25, 3775. DOI: https://doi.org/10.3390/molecules25173775.
- Yang, J. Y.; Bullock, R. M.; Dougherty, W. G.; Kassel, W. S.; Twamley, B.; DuBois, D. L.; DuBois, M. R. Reduction of Oxygen Catalyzed by Nickel Diphosphine Complexes with Positioned Pendant Amines. Dalton Trans. 2010, 39, 3001–3010. DOI: https://doi.org/10.1039/B921245K.
- Smith, S. E.; Yang, J. Y.; DuBois, D. L.; Bullock, R. M. Reversible Electrocatalytic Production and Oxidation of Hydrogen at Low Overpotentials by a Functional Hydrogenase Mimic. Angew. Chem. Int. Ed. 2012, 51, 3152–3155. DOI: https://doi.org/10.1002/anie.201108461.
- Klug, C. M.; O’Hagan, M.; Bullock, R. M.; Appel, A. M.; Wiedner, E. S. Impact of Weak Agostic Interactions in Nickel Electrocatalysts for Hydrogen Oxidation. Organometallics 2017, 36, 2275–2284. DOI: https://doi.org/10.1021/acs.organomet.7b00103.
- Karasik, A. A.; Naumov, R. N.; Sinyashin, O. G.; Belov, G. P.; Novikova, H. V.; Lönnecke, P.; Hey-Hawkins, E. Novel Chiral 1,5-Diaza-3,7-Diphosphacyclooctane Ligands and Their Transition Metal Complexes. Dalton Trans. 2003, 2209–2214. DOI: https://doi.org/10.1039/B300754E.
- Franz, J. A.; O’Hagan, M.; Ho, M.-H.; Liu, T.; Helm, M. L.; Lense, S.; DuBois, D. L.; Shaw, W. J.; Appel, A. M.; Raugei, S.; Bullock, R. M. Conformational Dynamics and Proton Relay Positioning in Nickel Catalysts for Hydrogen Production and Oxidation. Organometallics 2013, 32, 7034–7042. DOI: https://doi.org/10.1021/om400695w.
- Karasik, A. A.; Nikonov, G. N.; Arbuzov, B. A.; Musin, R. Z.; Efremov, Y. Y. Synthesis and Several Properties of 1,3,2,5-Dioxaboraphosphorinanes with a Branched Substituent at the Boron Atom. Russ. Chem. Bull. 1991, 40, 633–637. DOI: https://doi.org/10.1007/BF00958010.
- Fraze, K.; Wilson, A. D.; Appel, A. M.; DuBois, M. R.; DuBois, D. L. Thermodynamic Properties of the Ni − H Bond in Complexes of the Type [HNi(P2RN2R′)2](BF4) and Evaluation of Factors That Control Catalytic Activity for Hydrogen Oxidation/Production. Organometallics 2007, 26, 3918–3924. DOI: https://doi.org/10.1021/om070143v.
- Khrizanforova, V. V.; Musina, E. I.; Khrizanforov, M. N.; Gerasimova, T. P.; Katsyuba, S. A.; Spiridonova, Y. S.; Islamov, D. R.; Kataeva, O. N.; Karasik, A. A.; Sinyashin, O. G.; Budnikova, Y. H. Unexpected Ligand Effect on the Catalytic Reaction Rate Acceleration for Hydrogen Production Using Biomimetic Nickel Electrocatalysts with 1,5-Diaza-3,7-Diphosphacyclooctanes. J. Organomet. Chem. 2015, 789-790, 14–21. DOI: https://doi.org/10.1016/j.jorganchem.2015.04.044.
- Tran, P. D.; Goff, A.; Heidkamp, J.; Jousselme, B.; Guillet, N.; Palacin, S.; Dau, H.; Fontecave, M.; Artero, V. Noncovalent Modification of Carbon Nanotubes with Pyrene-Functionalized Nickel Complexes: Carbon Monoxide Tolerant Catalysts for Hydrogen Evolution and Uptake. Angew. Chem. Int. Ed. 2011, 50, 1371–1374. DOI: https://doi.org/10.1002/ange.201005427.
- Spiridonova, J. S.; Karasik, A. A.; Sinyashin, O. G. The First Example of Diazadiphosphacyclooctanes with Bicyclic Substituents. Phosphorus Sulfur Silicon Relat. Elem 2011, 186, 764–765. DOI: https://doi.org/10.1080/10426507.2010.509880.
- Brunner, F. M. Interactions of Immobilized Transition Metal Complexes with Electrode Surfaces and Their Implications for Catalysis. Ph.D. Dissertation, University of California, San Diego, California, U.S, 2021.
- Bridge, B. Iron(II) Metal-Ligand Cooperative Catalysts for Endo-Selective Intramolecular Hydrofunctionalization. MSc Dissertation, University of Western Ontario, London, Canada, 2020.
- Latypov, S.; Strelnik, A.; Balueva, A.; Spiridonova, Y.; Karasik, A.; Sinyashin, O. Conformational Analysis of P,N-Containing Eight-Membered Heterocycles and Their Pt/Ni Complexes in Solution. Eur. J. Inorg. Chem. 2016, 1068–1084. DOI: https://doi.org/10.1002/ejic.201501331.
- Isbrandt, E. S.; Nasim, A.; Zhao, K.; Newman, S. G. Catalytic Aldehyde and Alcohol Arylation Reactions Facilitated by a 1,5-Diaza-3,7-Diphosphacyclooctane Ligand. J. Am. Chem. Soc. 2021, 143, 14646–14656. DOI: https://doi.org/10.1021/jacs.1c05661.
- Das, P.; Stolley, R. M.; Eide, E. F.; Helm, M. L. A NiII–Bis(Diphosphine)–Hydride Complex Containing Proton Relays – Structural Characterization and Electrocatalytic Studies. Eur. J. Inorg. Chem. 2014, 4611–4618. DOI: https://doi.org/10.1002/ejic.201402250.
- Kilgore, U. J.; Stewart, M. P.; Helm, M. L.; Dougherty, W. G.; Kassel, W. S.; DuBois, M. R.; DuBois, D. L.; Bullock, R. M. Studies of a Series of [Ni(PR2NPh2)2(CH3CN)]2+ Complexes as Electrocatalysts for H2 Production: Substituent Variation at the Phosphorus Atom of the P2N2 Ligand. Inorg. Chem. 2011, 50, 10908–10918. DOI: https://doi.org/10.1021/ic201461a.
- Wiedner, S.; Yang, J. Y.; Dougherty, W. G.; Kassel, W. S.; Bullock, R. M.; DuBois, M. R.; DuBois, D. L. Comparison of Cobalt and Nickel Complexes with Sterically Demanding Cyclic Diphosphine Ligands: Electrocatalytic H2 Production by [Co(PtBu2NPh2)(CH3CN)3](BF4)2. Organometallics 2010, 29, 5390–5401. DOI: https://doi.org/10.1021/om100395r.
- Orthaber, A.; Karnahl, M.; Tschierlei, S.; Streich, D.; Stein, M.; Ott, S. Coordination and Conformational Isomers in Mononuclear Iron Complexes with Pertinence to the [FeFe] Hydrogenase Active Site. Dalton Trans. 2014, 43, 4537–4549. DOI: https://doi.org/10.1039/C3DT53268B.
- Strelnik, I. D.; Dayanova, I. R.; Kolesnikov, I. E.; Fayzullin, R. R.; Litvinov, I. A.; Samigullina, A. I.; Gerasimova, T. P.; Katsyuba, S. A.; Musina, E. I.; Karasik, A. A. The Assembly of Unique Hexanuclear Copper(I) Complexes with Effective White Luminescence. Inorg. Chem. 2019, 58, 1048–1057. DOI: https://doi.org/10.1021/acs.inorgchem.8b01862.
- Wiedner, E. S.; Roberts, J. A. S.; Dougherty, W. G.; Kassel, W. S.; DuBois, D. L.; Bullock, R. M. Synthesis and Electrochemical Studies of Cobalt(III) Monohydride Complexes Containing Pendant Amines. Inorg. Chem. 2013, 52, 9975–9988. DOI: https://doi.org/10.1021/ic401232g.
- Prokopchuk, D. E.; Wiedner, E. S.; Walter, E. D.; Popescu, C. V.; Piro, N. A.; Kassel, W. S.; Bullock, R. M.; Mock, M. T. Catalytic N2 Reduction to Silylamines and Thermodynamics of N2 Binding at Square Planar Fe. J. Am. Chem. Soc. 2017, 139, 9291–9301. DOI: https://doi.org/10.1021/jacs.7b04552.
- Fihri, A.; Luart, D.; Len, C.; Solhy, A.; Chevrin, C.; Polshettiwar, V. Suzuki–Miyaura Cross-Coupling Coupling Reactions with Low Catalyst Loading: A Green and Sustainable Protocol in Pure Water. Dalton Trans. 2011, 40, 3116–3121. DOI: https://doi.org/10.1039/c0dt01637c.
- Ignatieva, S. N.; Balueva, A. S.; Karasik, A. A.; Latypov, S. K.; Nikonova, A. G.; Naumova, O. E.; Lönnecke, P.; Hey-Hawkins, E.; Sinyashin, O. G. First Representative of Optically Active P-L-Menthyl-Substituted (Aminomethyl)Phosphine and Its Borane and Metal Complexes. Inorg. Chem. 2010, 49, 5407–5412. DOI: https://doi.org/10.1021/ic902564n.
- Nasybullina, G. R.; Yanilkin, V. V.; Ziganshina, A. Y.; Morozov, V. I.; Sultanova, E. D.; Korshin, D. E.; Spiridonova, Y. S.; Balueva, A. S.; Karasik, A. A.; Konovalov, A. I. Electrochemical Switching of Monomer—Associate in the System Tetraviologen Calix[4]Resorcinol—3,7-Di(l-Menthyl)-1,5-di(p-Sulfonatophenyl)-1,5-Diaza-3,7-Diphosphacyclooctane. Russ. Chem. Bull. 2013, 62, 2158–2170. DOI: https://doi.org/10.1007/s11172-013-0315-7.
- Baimukhametov, F. Z.; Zheltukhin, V. F.; Nikonov, G. N.; Balueva, A. S. Synthesis of New Phosphines and P-Heterocycles from Phosphonates Containing Allyl Group. Russ. J. Gen. Chem. (Engl. Transl.) 2002, 72, 1754–1759. DOI: https://doi.org/10.1023/A:1023345313956.
- Seu, C. S.; Appel, A. M.; Doud, M. D.; DuBois, D. L.; Kubiak, C. P. Formate Oxidationvia β-Deprotonation in [Ni(PR2NR′2)2(CH3CN)]2+ Complexes. Energy Environ. Sci. 2012, 5, 6480–6490. DOI: https://doi.org/10.1039/c2ee03341k.
- Seu, C. S. Towards an Artificial Formate Dehydrogenase: Mechanistic Studies of Formate Oxidation and CO2 Reduction by Metal P2N2 Complexes. Ph.D. Dissertation, University of California, San Diego, U.S., 2013.
- Boulanger, J.; Bricout, H.; Tilloy, S.; Fihri, A.; Len, C.; Hapiot, F.; Monflier, E. Water-Soluble Diphosphadiazacyclooctanes as Ligands for Aqueous Organometallic Catalysis. Catal. Commun 2012, 29, 77–81. DOI: https://doi.org/10.1016/j.catcom.2012.09.019.
- Liu, T.; Wang, X.; Hoffmann, C.; DuBois, D. L.; Bullock, R. M. Heterolytic Cleavage of Hydrogen by an Iron Hydrogenase Model: An Fe–H.H–N Dihydrogen Bond Characterized by Neutron Diffraction. Angew. Chem. Int. Ed. 2014, 53, 5300–5304. DOI: https://doi.org/10.1002/anie.201402090.
- Weiss, C. J.; Wiedner, E. S.; Roberts, J. A. S.; Appel, A. M. Nickel Phosphine Catalysts with Pendant Amines for Electrocatalytic Oxidation of Alcohols. Chem. Commun. 2015, 51, 6172–6174. DOI: https://doi.org/10.1039/c5cc01107h.
- Strelnik, I. D.; Musina, E. I.; Ignatieva, S. N.; Balueva, A. S.; Gerasimova, T. P.; Katsyuba, S. A.; Krivolapov, D. B.; Dobrynin, A. B.; Bannwarth, C.; Grimme, S.; et al. Pyridyl Containing 1,5-Diaza-3,7-Diphosphacyclooctanes as Bridging Ligands for Dinuclear Copper(I) Complexes. Z Anorg. Allg. Chem. 2017, 643, 895–902. DOI: https://doi.org/10.1002/zaac.201700049.
- Strelnik, I. D. New Pyridyl-Containing Cyclic Aminomethylphosphines and Their Complexes with Metals of Nickel and Copper Subgroups. Ph.D. Dissertation, A. E. Arbuzov Institute of Organic and Physical Chemistry, Russian Federation, Kazan, 2013.
- Yang, J. Y.; Chen, S.; Dougherty, W. G.; Kassel, W. S.; Bullock, R. M.; DuBois, D. L.; Raugei, S.; Rousseau, R.; Dupuis, M.; DuBois, M. R. Hydrogen Oxidation Catalysis by a Nickel Diphosphine Complex with Pendant tert-Butyl Amines. Chem. Commun. 2010, 46, 8618–8620. DOI: https://doi.org/10.1039/c0cc03246h.
- Wilson, A. D.; Newell, R. H.; McNevin, M. J.; Muckerman, J. T.; DuBois, M. R.; DuBois, D. L. Hydrogen Oxidation and Production Using Nickel-Based Molecular Catalysts with Positioned Proton Relays. J. Am. Chem. Soc. 2006, 128, 358–366. DOI: https://doi.org/10.1021/ja056442y.
- O’Hagan, M.; Shaw, W. J.; Raugei, S.; Chen, S.; Yang, J. Y.; Kilgore, U. J.; DuBois, D. L.; Bullock, R. M. Moving Protons with Pendant Amines: Proton Mobility in a Nickel Catalyst for Oxidation of Hydrogen. J. Am. Chem. Soc. 2011, 133, 14301–14312. DOI: https://doi.org/10.1021/ja201838x.
- Das, P.; Ho, M.-H.; O'Hagan, M.; Shaw, W. J.; Bullock, R. M.; Raugei, S.; Helm, M. L. Controlling Proton Movement: Electrocatalytic Oxidation of Hydrogen by a Nickel(II) Complex Containing Proton Relays in the Second and Outer Coordination Spheres. Dalton Trans. 2014, 43, 2744–2754. DOI: https://doi.org/10.1039/C3DT53074D.
- Dutta, A.; Lense, S.; Hou, J.; Engelhard, M. H.; Roberts, J. A. S.; Shaw, W. J. Minimal Proton Channel Enables H2 Oxidation and Production with a Water-Soluble Nickel-Based Catalyst. J. Am. Chem. Soc. 2013, 135, 18490–18496. DOI: https://doi.org/10.1021/ja407826d.
- Boralugodage, N. P.; Arachchige, R. J.; Dutta, A.; Buchko, G. W.; Shaw, W. J. Evaluating the Role of Acidic, Basic, and Polar Amino Acids and Dipeptides on a Molecular Electrocatalyst for H2 Oxidation. Catal. Sci. Technol. 2017, 7, 1108–1121. DOI: https://doi.org/10.1039/C6CY02579J.
- Dutta, A.; Roberts, J. A. S.; Shaw, W. J. Arginine-Containing Ligands Enhance H2 Oxidation Catalyst Performance. Angew. Chem. Int. Ed. 2014, 53, 6487–6491. DOI: https://doi.org/10.1002/anie.201402304.
- Dutta, A.; DuBois, D. L.; Roberts, J. A. S.; Shaw, W. J. Amino Acid Modified Ni Catalyst Exhibits Reversible H2 Oxidation/Production over a Broad pH Range at Elevated Temperatures. PNAS. 2014, 111, 16286–16291. DOI: https://doi.org/10.1073/pnas.1416381111.
- Priyadarshani, N.; Dutta, A.; Ginovska, B.; Buchko, G. W.; O’Hagan, M.; Raugei, S.; Shaw, W. J. Achieving Reversible H2/H+ Interconversion at Room Temperature with Enzyme-Inspired Molecular Complexes: A Mechanistic Study. ACS Catal. 2016, 6, 6037–6049. DOI: https://doi.org/10.1021/acscatal.6b01433
- Lense, S.; Ho, M.-H.; Chen, S.; Jain, A.; Raugei, S.; Linehan, J. C.; Roberts, J. A. S.; Appel, A. M.; Shaw, W. Incorporating Amino Acid Esters into Catalysts for Hydrogen Oxidation: Steric and Electronic Effects and the Role of Water as a Base. Organometallics 2012, 31, 6719–6731. DOI: https://doi.org/10.1021/om300409y.
- Lense, S.; Dutta, A.; Roberts, J. A. S.; Shaw, W. J. A Proton Channel Allows a Hydrogen Oxidation Catalyst to Operate at a Moderate Overpotential with Water Acting as a Base. Chem. Commun. 2014, 50, 792–795. DOI: https://doi.org/10.1039/C3CC46829A.
- Coutard, N.; Reuillard, B.; Huan, T. N.; Valentino, F.; Jane, R. T.; Gentil, S.; Andreiadis, E. S.; Le Goff, A.; Asset, T.; Maillard, F.; et al. Impact of Ionomer Structuration on the Performance of Bio-Inspired Noble-Metal-Free Fuel Cell Anodes. Chem. Catal. 2021, 1, 88–105. DOI: https://doi.org/10.1016/j.checat.2021.01.001.
- Karasik, A. A.; Spiridonova, Y. S.; Yakhvarov, D. G.; Sinyashin, O. G.; Lönnecke, P.; Sommer, R.; Hey-Hawkins, E. Synthesis and Molecular Structure of a Chiral Ferrocenylphosphine. Mendeleev Commun. 2005, 15, 89–90. DOI: https://doi.org/10.1070/MC2005v015n03ABEH002119.
- Song, L.-C.; Tan, H.; Luo, F.-X.; Wang, Y.-X.; Ma, Z.; Niu, Z. Synthesis, Structural Characterization, and Catalytic H2 Production of Ferrocenyl (Fc) Group Containing Complexes [Ni(PFc2NAr)2](BF4)2 (Ar = Ph, p-BrC6H4). Organometallics 2014, 33, 5246–5253. DOI: https://doi.org/10.1021/om500571n.
- Karasik, A. A.; Musina, E. I.; Balueva, A. S.; Strelnik, I. D.; Sinyashin, O. G. Cyclic Aminomethylphosphines as Ligands. Rational Design and Unpredicted Findings. Pure Appl. Chem. 2017, 89, 293–310. DOI: https://doi.org/10.1515/pac-2016-1022.
- Karasik, A. A. Cyclic Aminomethylphosphines as Ligands. Balancing between Rational Design and Unpredicted Findings. Phosphorus Sulfur Silicon Relat. Elem. 2016, 191, 1413–1415. DOI: https://doi.org/10.1080/10426507.2016.1211656.
- Arbuzov, B. A.; Erastov, O. A.; Nikonov, G. N. Method of Preparing 1,3-Azaphosphetidines. U.S.S.R. Patent 810,715, Mar 7, 1981.
- Arbuzov, B. A.; Erastov, O. A.; Nikonov, G. N. Method of Preparing 1,3-Azaphosphetidines. U.S.S.R. Patent 854,932, Aug 15, 1981.
- Arbuzov, B. A.; Erastov, O. A.; Nikonov, G. N. Synthesis of 1,3-Azaphosphetidines. Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 735–736.
- Arbuzov, B. A.; Nikonov, G. N. Phosphorus Heterocycles from α-Hydroxyalkylphosphines and Vinylphosphines. Adv. Heterocycl. Chem. 1994, 61, 59–140. DOI: https://doi.org/10.1016/S0065-2725(08)60897-1.
- Randaccio, L.; Zangrando, E.; Gei, M. H.; Giumanini, A. G. Revisitation of Formaldehyde-Aniline Condensation. III. The Cyclic Tetramer of N-Methyleneaniline: An X-Ray Diffraction Structure Determination. J. Prakt. Chem. 1987, 329, 187–194. DOI: https://doi.org/10.1002/prac.19873290204.
- Giumanini, A. G.; Verardo, G.; Zangrando, E.; Lassiani, L. Revisitation of Formaldehyde Aniline Condensation. VII. 1,3,5-Triarylhexahydro-Sym-Triazines and 1,3,5,7-Tetraaryl-1,3,5,7-Tetrazocines from Aromatic Amines and Paraformaldehyde. J. Prakt. Chem. 1987, 329, 1087–1103. DOI: https://doi.org/10.1002/prac.19873290619.
- Ghandi, M.; Salimi, F.; Olyaei, A. Novel Reaction of N,N'-Bisarylmethanediamines with Formaldehyde. Synthesis of Some New 1,3,5-Triaryl-1,3,5-Hexahydrotriazines. Molecules 2006, 11, 556–563. DOI: https://doi.org/10.3390/11070556.
- Doud, M. D.; Grice, K. A.; Lilio, A. M.; Seu, C. S.; Kubiak, C. P. Versatile Synthesis of PR2NR′2 Ligands for Molecular Electrocatalysts with Pendant Bases in the Second Coordination Sphere. Organometallics 2012, 31, 779–782. DOI: https://doi.org/10.1021/om201168h.
- Wiese, S.; Kilgore, U. J.; DuBois, D. L.; Bullock, R. M. [Ni(PMe2NPh2)2](BF4)2 as an Electrocatalyst for H2 Production. ACS Catal. 2012, 2, 720–727. DOI: https://doi.org/10.1021/cs300019h.
- Stubbs, J. M.; Bridge, B. J.; Blacquiere, J. M. Optimizing Ligand Structure for Low-Loading and Fast Catalysis for Alkynyl-Alcohol and -Amine Cyclization. Dalton Trans. 2019, 48, 7928–7937. DOI: https://doi.org/10.1039/c9dt01870k.
- Doud, M. D. Synthetic Advances for P2N2 Molecular Electrocatalysts with Pendant Bases in the Second Coordination Sphere. Ph.D. Dissertation, University of California, San Diego, U.S., 2016.
- Karasik, A. A.; Erastov, O. A.; Arbuzov, B. A. Reactions of Bis(α-Hydroxyalkyl)Phosphines with Iminoboranes. Russ. Chem. Bull. 1988, 37, 2172–2174. DOI: https://doi.org/10.1007/BF00953432.
- Nikonov, G. N.; Karasik, A. A.; Arbuzov, B. A. Synthesis and Properties of Triethylammonium 2,2,5-Triphenyl-1,3,2,5-Dioxaborataphosphorinane. Russ. Chem. Bull. 1992, 41, 1094–1099. DOI: https://doi.org/10.1007/BF00866594.
- Arbuzov, B. A.; Erastov, O. A.; Nikonov, G. N. 1,3-Azaphosphetidines and Their Praparation Method. U.S.S.R. Patent 785,316, Dec 7, 1980.
- Balueva, A. S.; Kuznetsov, R. M.; Litvinov, I. A.; Gubaidullin, A. T.; Nikonov, G. N. 1-[p-(p-Phenylenomethyl)Phenyl]-3,7-Diphenyl-1,5,3,7-Diazadiphosphacyclooctane} as the First Representative of a New Type of Nitrogen-Containing Macroheterocyclic Phosphines. Mendeleev Commun. 2000, 10, 120–121. DOI: https://doi.org/10.1070/MC2000v010n03ABEH001249.
- Kuznetsov, R. M.; Balueva, A. S.; Litvinov, I. A.; Gubaidullin, A. T.; Nikonov, G. N.; Karasik, A. A.; Sinyashin, O. G. Synthesis of New Macrocyclic Aminomethylphosphines Based on 4,4"-Diaminodiphenylmethane and Its Derivatives. Russ. Chem. Bull. 2002, 51, 151–156. DOI: https://doi.org/10.1023/A:1015086419302.
- Balueva, A. S.; Kuznetsov, R. M.; Ignat'eva, S. N.; Karasik, A. A.; Gubaidullin, A. T.; Litvinov, I. A.; Sinyashin, O. G.; Lönnecke, P.; Hey-Hawkins, E. Self-Assembly of Novel Macrocyclic Aminomethylphosphines with Hydrophobic Intramolecular Cavities. Dalton Trans. 2004, 442–447. DOI: https://doi.org/10.1039/B311592E.
- Nikolaeva, Y. A.; Balueva, A. S.; Musina, E. I.; Karasik, A. A.; Sinyashin, O. G. New P,N-Containing Cyclophanes with Exocyclic Pyridyl-Containing Substituents on Phosphorus Atoms. MHC. 2015, 8, 402–408. DOI: https://doi.org/10.6060/mhc150976b.
- Nikolaeva, Y. A. P,N-Containing Cyclophans and Their Complexes with Transition Metals of 6, 10, 11 Groups And with Quaternary Ammonium Salts. Ph.D. Dissertation, Arbuzov Institute of Organic and Physical Chemistry, Kazan, Russian Federation, 2019.
- Kulikov, D. V.; Karasik, A. A.; Balueva, A. S.; Kataeva, O. N.; Litvinov, I. A.; Hey-Hawkins, E.; Sinyashin, O. G. The First Representative of Novel 36-Membered P,N,O-Containing Cyclophanes. Mendeleev Commun. 2007, 17, 195–196. DOI: https://doi.org/10.1016/j.mencom.2007.06.001.
- Balueva, A. S.; Ignatieva, S. N.; Karasik, A. A.; Lönnecke, P.; Hey-Hawkins, E.-M.; Sinyashin, O. G. Optically Active Cage P,N-Containing Cyclophanes Based on L-Menthylphosphine and Their Platinum (II) and Palladium (II) Complexes. Phosphorus Sulfur Silicon Relat. Elem. 2011, 186, 891–893. DOI: https://doi.org/10.1080/10426507.2010.506668.
- Karasik, A. A.; Kulikov, D. V.; Balueva, A. S.; Ignat'eva, S. N.; Kataeva, O. N.; Lönnecke, P.; Kozlov, A. V.; Latypov, S. K.; Hey-Hawkins, E.; Sinyashin, O. G. P,N-Containing Cyclophanes with Large Helical Hydrophobic Cavities: Prospective Precursors for the Design of a Molecular Reactor. Dalton Trans. 2009, 490–494. DOI: https://doi.org/10.1039/B812508B.
- Nikolaeva, Y. A.; Balueva, A. S.; Ignat´Eva, S. N.; Musina, E. I.; Karasik, A. A. Synthesis of First Representatives of 46-Membered P,N,O-Containing Cyclophanes and Their Transition Metal Complexes. Russ. Chem. Bull. 2016, 65, 1319–1324. DOI: https://doi.org/10.1007/s11172-016-1455-3.
- Zhelezina, Y. A.; Balueva, A. S.; Ignatieva, S. N.; Karasik, A. A.; Sinyashin, O. G. Host-Guest Complexes of P,N-Containing Cyclophanes with Heteroaromatic Ammonium Salts in Solution. Phosphorus Sulfur Silicon Relat. Elem. 2013, 188, 19–20. DOI: https://doi.org/10.1080/10426507.2012.740701.
- Balueva, A. S.; Musina, E. I.; Nikolaeva, Y. A.; Karasik, A. A.; Sinyashin, O. G. Complexes of Phosphorus-Containing Cyclophanes and Cryptands with Metals, Anions, and Organic Substrates. Russ. J. Org. Chem. 2019, 55, 1642–1661. DOI: https://doi.org/10.1134/S1070428019110022.
- Karasik, A. A.; Kulikov, D. V.; Kuznetsov, R. M.; Balueva, A. S.; Akhmetgaliev, A. A.; Kataeva, O. N.; Lőnnecke, P.; Sharapov, O. R.; Zhelezina, Y. A.; Ignat’eva, S. N.; et al. Novel P,N-Containing Cyclophane with a Chiral Hydrophobic Cavity. Macroheterocycles 2011, 4, 324–330. DOI: https://doi.org/10.6060/mhc2011.4.08.
- Yang, J. Y.; Smith, S. E.; Liu, T.; Dougherty, W. G.; Hoffert, W. A.; Kassel, W. S.; DuBois, M. R.; DuBois, D. L.; Bullock, R. M. Two Pathways for Electrocatalytic Oxidation of Hydrogen by a Nickel Bis(Diphosphine) Complex with Pendant Amines in the Second Coordination Sphere. J. Am. Chem. Soc. 2013, 135, 9700–9712. DOI: https://doi.org/10.1021/ja400705a.
- Shaw, W. J.; Helm, M. L.; DuBois, D. L. A Modular, Energy-Based Approach to the Development of Nickel Containing Molecular Electrocatalysts for Hydrogen Production and Oxidation. Biochim. Biophys. Acta 2013, 1827, 1123–1139. DOI: https://doi.org/10.1016/j.bbabio.2013.01.003.
- DuBois, M. R.; DuBois, D. L. The Roles of the First and Second Coordination Spheres in the Design of Molecular Catalysts for H2 Production and Oxidation. Chem. Soc. Rev. 2009, 38, 62–72. DOI: https://doi.org/10.1039/B801197B.
- Bullock, R. M.; Helm, M. L. Molecular Electrocatalysts for Oxidation of Hydrogen Using Earth-Abundant Metals: Shoving Protons around with Proton Relays. Acc. Chem. Res. 2015, 48, 2017–2026. DOI: https://doi.org/10.1021/acs.accounts.5b00069.
- Raugei, S.; Helm, M. L.; Hammes-Schiffer, S.; Appel, A. M.; O'Hagan, M.; Wiedner, E. S.; Bullock, R. M. Experimental and Computational Mechanistic Studies Guiding the Rational Design of Molecular Electrocatalysts for Production and Oxidation of Hydrogen. Inorg. Chem. 2016, 55, 445–460. DOI: https://doi.org/10.1021/acs.inorgchem.5b02262.
- Budnikova, Y. H.; Khrizanforova, V. V. Synthetic Models of Hydrogenases Based on Framework Structures Containing Coordinating P,N-Atoms as Hydrogen Energy Electrocatalysts – from Molecules to Materials. Pure Appl. Chem. 2020, 92, 1305–1320. DOI: https://doi.org/10.1515/pac-2019-1207.
- Kireev, N. V.; Kiryutin, A. S.; Pavlov, A. A.; Yurkovskaya, A. V.; Musina, E. I.; Karasik, A. A.; Shubina, E. S.; Ivanov, K. L.; Belkova, N. V. Nickel(II) Dihydrogen and Hydride Complexes as the Intermediates of H2 Heterolytic Splitting by Nickel Diazadiphosphacyclooctane Complexes. Eur. J. Inorg. Chem. 2021, 2021, 4265–4272. DOI: https://doi.org/10.1002/ejic.202100489.
- Xue, L.; Ahlquist, M. S. G. A DFT Study: Why Do [Ni(PR2NR′2)2]2+ Complexes Facilitate the Electrocatalytic Oxidation of Formate? Inorg. Chem. 2014, 53, 3281–3289. DOI: https://doi.org/10.1021/ic4027317.
- Chen, X.; Yang, X. Bioinspired Design and Computational Prediction of Iron Complexes with Pendant Amines for the Production of Methanol from CO2 and H2. J. Phys. Chem. Lett. 2016, 7, 1035–1041. DOI: https://doi.org/10.1021/acs.jpclett.6b00161.
- Bruch, Q. J.; Connor, G. P.; McMillion, N. D.; Goldman, A. S.; Hasanayn, F.; Holland, P. L.; Miller, A. J. M. Considering Electrocatalytic Ammonia Synthesis via Bimetallic Dinitrogen Cleavage. ACS Catal. 2020, 10, 10826–10846. DOI: https://doi.org/10.1021/acscatal.0c02606.
- Karasik, A. A.; Musina, E. I.; Strelnik, I. D.; Balueva, A. S.; Budnikova, Y. H.; Sinyashin, O. G. Cyclic Phosphino Amino Pyridines - Novel Instrument for Construction of Catalysts and Luminescent Materials. Phosphorus Sulfur Silicon Relat. Elem. 2015, 190, 729–732. DOI: https://doi.org/10.1080/10426507.2014.989431.
- Karasik, A. A.; Strelnik, I. D.; Musina, E. I.; Dayanova, I. R.; Elistratova, J. G.; Mustafina, A. R.; Sinyashin, O. G. Luminescent Complexes of 1,5-Diaza-3,7-Diphosphacyclooctanes with Coinage Metals. Phosphorus Sulfur Silicon Relat. Elem. 2019, 194, 410–414. DOI: https://doi.org/10.1080/10426507.2018.1539854.
- Karasik, A. A.; Musina, E. I.; Strelnik, I. D.; Dayanova, I. R.; Elistratova, J. G.; Mustafina, A. R.; Sinyashin, O. G. Luminescent Complexes on a Scaffold of P2N2-Ligands: Design of Materials for Analytical and Biomedical Applications. Pure Appl. Chem. 2019, 91, 839–849. DOI: https://doi.org/10.1515/pac-2018-0926.
- Strelnik, I. D.; Sizov, V. V.; Gurzhiy, V. V.; Melnikov, A. S.; Kolesnikov, I. E.; Musina, E. I.; Karasik, A. A.; Grachova, E. V. Binuclear Gold(I) Phosphine Alkynyl Complexes Templated on a Flexible Cyclic Phosphine Ligand: Synthesis and Some Features of Solid-State Luminescence. Inorg. Chem. 2020, 59, 244–253. DOI: https://doi.org/10.1021/acs.inorgchem.9b02091.
- Dayanova, I. R.; Shamsieva, A. V.; Strelnik, I. D.; Gerasimova, T. P.; Kolesnikov, I. E.; Fayzullin, R. R.; Islamov, D. R.; Saifina, A. F.; Musina, E. I.; Hey-Hawkins, E.; Karasik, A. A. Assembly of Heterometallic AuICu2I2 Cores on the Scaffold of NPPN-Bridging Cyclic Bisphosphine. Inorg. Chem. 2021, 60, 5402–5411. DOI: https://doi.org/10.1021/acs.inorgchem.1c00442.
- Das, A. K.; Engelhard, M. H.; Bullock, R. M.; Roberts, J. A. S. A Hydrogen-Evolving Ni(P2N2)2 Electrocatalyst Covalently Attached to a Glassy Carbon Electrode: Preparation, Characterization, and Catalysis. Comparisons with the Homogeneous Analogue. Inorg. Chem. 2014, 53, 6875–6885. DOI: https://doi.org/10.1021/ic500701a.
- Huan, T. N.; Jane, R. T.; Benayad, A.; Guetaz, L.; Tran, P. D.; Artero, V. Bio-Inspired Noble Metal-Free Nanomaterials Approaching Platinum Performances for H2 Evolution and Uptake. Energy Environ. Sci. 2016, 9, 940–947. DOI: https://doi.org/10.1039/C5EE02739J.
- Galan, B. R.; Reback, M. L.; Jain, A.; Appel, A. M.; Shaw, W. J. Electrocatalytic Oxidation of Formate with Nickel Diphosphine Dipeptide Complexes: Effect of Ligands Modified with Amino Acids. Eur. J. Inorg. Chem. 2013, 5366–5371. DOI: https://doi.org/10.1002/ejic.201300751.
- Jain, A.; Reback, M. L.; Lindstrom, M. L.; Thogerson, C. E.; Helm, M. L.; Appel, A. M.; Shaw, W. J. Investigating the Role of the Outer-Coordination Sphere in [Ni(PPh2NPh-R2)2]2+ Hydrogenase Mimics. Inorg. Chem. 2012, 51, 6592–6602. DOI: https://doi.org/10.1021/ic300149x.
- Gross, M. A.; Reynal, A.; Durrant, J. R.; Reisner, E. Versatile Photocatalytic Systems for H2 Generation in Water Based on an Efficient DuBois-Type Nickel Catalyst. J. Am. Chem. Soc. 2014, 136, 356–366. DOI: https://doi.org/10.1021/ja410592d.
- Caputo, C. A.; Gross, M. A.; Lau, V. W.; Cavazza, C.; Lotsch, B. V.; Reisner, E. Photocatalytic Hydrogen Production Using Polymeric Carbon Nitride with a Hydrogenase and a Bioinspired Synthetic Ni Catalyst. Angew. Chem. Int. Ed. 2014, 53, 11538–11542. DOI: https://doi.org/10.1002/anie.201406811.
- Martindale, B. C. M.; Hutton, G. A. M.; Caputo, C. A.; Reisner, E. Solar Hydrogen Production Using Carbon Quantum Dots and a Molecular Nickel Catalyst. J. Am. Chem. Soc. 2015, 137, 6018–6025. DOI: https://doi.org/10.1021/jacs.5b01650.
- Rosser, T. E.; Gross, M. A.; Lai, Y.-H.; Reisner, E. Precious-Metal Free Photoelectrochemical Water Splitting with Immobilised Molecular Ni and Fe Redox Catalysts. Chem. Sci. 2016, 7, 4024–4035. DOI: https://doi.org/10.1039/C5SC04863J.
- Gross, M. A.; Creissen, C. E.; Orchard, K. L.; Reisner, E. Photoelectrochemical Hydrogen Production in Water Using a Layer-by-Layer Assembly of a Ru Dye and Ni Catalyst on NiO. Chem. Sci. 2016, 7, 5537–5546. DOI: https://doi.org/10.1039/C6SC00715E.
- Creissen, C. E.; Warnan, J.; Reisner, E. Solar H2 Generation in Water with a CuCrO2 Photocathode Modified with an Organic Dye and Molecular Ni Catalyst. Chem. Sci. 2018, 9, 1439–1447. DOI: https://doi.org/10.1039/C7SC04476C.
- Rosser, T. E.; Hisatomi, T.; Sun, S.; Antón-García, D.; Minegishi, T.; Reisner, E.; Domen, K. La5Ti2Cu0.9Ag0.1S5O7 Modified with a Molecular Ni Catalyst for Photoelectrochemical H2 Generation. Chemistry 2018, 24, 18393–18397. DOI: https://doi.org/10.1002/chem.201801169.
- Karasik, A. A.; Musina, E. I.; Balueva, A. S.; Sinyashin, O. G. Novel Biomimetic Cyclic P,N-Ligands. Lability of P-CH2-N Fragment: Problem or Advantage? Phosphorus Sulfur Silicon Relat. Elem 2013, 188, 27–28. DOI: https://doi.org/10.1080/10426507.2012.741156.
- Strelnik, I. D.; Dayanova, I. R.; Poryvaev, T. M.; Gerasimova, T. P.; Litvinov, I. A.; Katsyuba, S. A.; Musina, E. I.; Karasik, A. A.; Sinyashin, O. G. Rearrangement of Two 8-Membered 1,5-Diaza-3,7-Diphosphacyclooctane Rings into 16-Membered P4N4 Ligand on the Gold(I) Template. Mendeleev Commun. 2020, 30, 40–42. DOI: https://doi.org/10.1016/j.mencom.2020.01.013.
- Mock, M. T.; Chen, S.; O'Hagan, M.; Rousseau, R.; Dougherty, W. G.; Kassel, W. S.; Bullock, R. M. Dinitrogen Reduction by a Chromium(0) Complex Supported by a 16-Membered Phosphorus Macrocycle. J. Am. Chem. Soc. 2013, 135, 11493–11496. DOI: https://doi.org/10.1021/ja405668u.
- Kendall, A. J.; Johnson, S. I.; Bullock, R. M.; Mock, M. T. Catalytic Silylation of N2 and Synthesis of NH3 and N2H4 by Net Hydrogen Atom Transfer Reactions Using a Chromium P4 Macrocycle. J. Am. Chem. Soc. 2018, 140, 2528–2536. DOI: https://doi.org/10.1021/jacs.7b11132.
- Fluck, E.; Weißgraeber, H.-J. 7-Methyl-1,3,5-Triaza-7-Phosphaadamantan-7-Ium-Jodid. Chem. Ztg. 1977, 101, 304–304.
- Caporali, M.; Gonsalvi, L.; Zanobini, F.; Peruzzini, M.; Putman, R. D.; Rauchfuss, T. B. Synthesis of the Water-Soluble Bidentate (P,N) Ligand PTN(Me) (PTN(Me) = 7-Phospha-3-Methyl-1,3,5-Triazabicyclo[3.3.1]Nonane). In Inorganic Syntheses; Rauchfuss, T. B., Ed.; John Wiley & Sons: Hoboken, NJ, 2010; Vol. 35, pp. 96–102. DOI: https://doi.org/10.1002/9780470651568.ch5.
- Assmann, B.; Angermaier, K.; Paul, M.; Riede, J.; Schmidbaur, H. Synthesis of 7-Alkyl/Aryl-1,3,5-Triaza-7-Phosphonia-Adamantane Cations and Their Reductive Cleavage to Novel N-Methyl-P-Alkyl/Aryl[3.3.1]Bicyclononane Ligands. Chem. Ber. 1995, 128, 891–900. DOI: https://doi.org/10.1002/cber.19951280907.
- Kirk, A. S. Reactions of Novel Self-Assembled Iron(II) Phosphine Complexes. Ph.D. Dissertation, University of Bath, United Kingdom, 2008.
- Jogun, K. H.; Stezowski, J. J.; Fluck, E.; Weißgraeber, H.-J. Molekülstruktur des 7-Methyl-1.3.5-triaza-7-phosphaadamantan-7-ium-tetrafluoroborats. Darstellung und Charakterisierung des 7-Methyl-1.3.5-triaza-7-phospha-tricyclo[3.3.2.13,7]-undecan-7-ium-iodids. Z. Naturforsch. B 1978, 33, 1257–1262.
- Assmann, B.; Angermaier, K.; Schmidbaur, H. Synthesis, Structure and Complexes of a New Bicyclic N,P-Ligand Derived from Phosphatriazaadamantane. J. Chem. Soc, Chem. Commun. 1994, 941–942. DOI: https://doi.org/10.1039/c39940000941.
- Burrows, A. D.; Harrington, R. W.; Kirk, A. S.; Mahon, M. F.; Marken, F.; Warren, J. E.; Whittlesey, M. K. Synthesis, Characterization, and Electrochemistry of a Series of Iron(II) Complexes Containing Self-Assembled 1,5-Diaza-3,7-Diphosphabicyclo[3.3.1]Nonane Ligands. Inorg. Chem. 2009, 48, 9924–9935. DOI: https://doi.org/10.1021/ic900874f.
- Kostyanovskii, R. G.; Él'natanov, Y. I.; Shikhaliev, S. M.; Ignatov, S. M.; Chervin, I. I. Geminal Systems. 19. Reactions of Aminomethylphosphines with Electrophilic Reagents. Russ. Chem. Bull. 1982, 31, 1433–1441. DOI: https://doi.org/10.1007/BF00954168.
- Valyaev, D. A.; Filippov, O. A.; Lugan, N.; Lavigne, G.; Ustynyuk, N. A. Umpolung of Methylenephosphonium Ions in Their Manganese Half-Sandwich Complexes and Application to the Synthesis of Chiral Phosphorus-Containing Ligand Scaffolds. Angew. Chem. 2015, 127, 6413–6417. DOI: https://doi.org/10.1002/ange.201501256.
- Valyaev, D. A.; Willot, J.; Mangin, L. P.; Zargarian, D.; Lugan, N. Manganese-Mediated Synthesis of an NHC Core Non-Symmetric Pincer Ligand and Evaluation of Its Coordination Properties. Dalton Trans. 2017, 46, 10193–10196. DOI: https://doi.org/10.1039/C7DT02190A.
- Brill, M.; Kühnel, E.; Scriban, C.; Rominger, F.; Hofmann, P. A Short and Modular Synthesis of Bulky and Electron-Rich N-Phosphinomethyl-Functionalised N-Heterocyclic Carbene Complexes. Dalton Trans. 2013, 42, 12861–12864. DOI: https://doi.org/10.1039/C3DT51777B.
- LaPointe, A. M. Parallel Synthesis of Aminomethylphosphine Ligands. J. Comb. Chem. 1999, 1, 101–104. DOI: https://doi.org/10.1021/cc980013x.
- LaPointe, A. M.; Guram, A.; Powers, T. S.; Jandeleit, B.; Boussie, T.; Lund, C. Substituted Aminomethylphosphines, Compositions and Coordination Complexes of Same, Their Synthesis and Processes Using Same. U.S. Patent 6,043,363, Mar 28, 2000.
- Bowes, E. G.; Beattie, D. D.; Love, J. A. Role of Phosphine Sterics in Strained Aminophosphine Chelate Formation. Inorg. Chem. 2019, 58, 2925–2929. DOI: https://doi.org/10.1021/acs.inorgchem.8b03514.
- Grim, S. O.; Matienzo, L. J. The Synthesis and Characterization of Some Novel Polydentate Phosphorus-Nitrogen Ligands. Tetrahedron Lett. 1973, 14, 2951–2953. DOI: https://doi.org/10.1016/S0040-4039(01)96290-2.
- Kellner, K.; Tzschach, A.; Nagy-Magos, Z.; Markó, L. Optisch Aktive N-Phosphinomethylierte α-Aminosäuren: Synthese und Anwendung als Liganden in Asymmetrischen Hydrierungen mit Rhodium-Komplexen. J. Organomet. Chem. 1980, 193, 307–314. DOI: https://doi.org/10.1016/S0022-328X(00)90290-0.
- Law, D. J. The Synthesis of Aminomethylphosphines, Their Metal Complexes and Their Use in Homogeneous Catalysis. Ph.D. Dissertation, University of Leicester, Leicester, UK, 1990.
- Li, Q.-S.; Xu, F.-B.; Cui, D.-J.; Yu, K.; Zeng, X.-S.; Leng, X.-B.; Song, H.-B.; Zhang, Z.-Z. Heterobimetallic Pt(II)–M(I) (M = Cu, Ag) Eight-Membered Macrocyclic Complexes with Large-Bite P,N-Ligand Bridges. Dalton Trans. 2003, 1551–1557. DOI: https://doi.org/10.1039/b211301p.
- Cui, D.-J.; Li, Q.-S.; Xu, F.-B.; Leng, X.-B.; Zhang, Z.-Z. First Heterobimetallic Seven-Membered Macrocycle Complex with a Fe(0) → Cu(I) Donor − Acceptor Bond. Organometallics 2001, 20, 4126–4128. DOI: https://doi.org/10.1021/om010382x.
- Clarke, D. A.; Miller, P. W.; Long, N. J.; White, A. J. P. Steric Control over the Formation of Cis and Trans Bis-Chelated Palladium(II) Complexes Using a New Series of Flexible N,P Pyridyl–Phosphine Ligands. Dalton Trans. 2007, 4556–4564. DOI: https://doi.org/10.1039/b709032c.
- Bárta, O.; Císařová, I.; Štěpnička, P. Phosphinomethylation of [1′-(Diphenylphosphino)Ferrocenyl]-Methylamines as a Route to Unsymmetric Ferrocene Diphosphine Ligands. J. Organomet. Chem. 2018, 855, 26–32. DOI: https://doi.org/10.1016/j.jorganchem.2017.11.024.
- Deng, L.; Kang, B.; Englert, U.; Klankermayer, J.; Palkovits, R. Direct Hydrogenation of Biobased Carboxylic Acids Mediated by a Nitrogen-Centered Tridentate Phosphine Ligand. ChemSusChem 2016, 9, 177–180. DOI: https://doi.org/10.1002/cssc.201501461.
- Noble, T. A. Co‒ordination Studies of Polyarene and Halocarbon Functionalised Tertiary Phosphines for Explosives Detection. Ph.D. Dissertation, Loughborough University, Loughborough, UK, 2014.
- Komarnicka, U. K.; Kozieł, S.; Starosta, R.; Kyzioł, A. Selective Cu(I) Complex with Phosphine-Peptide (SarGly) Conjugate Contra Breast Cancer: Synthesis, Spectroscopic Characterization and Insight into Cytotoxic Action. J. Inorg. Biochem. 2018, 186, 162–175. DOI: https://doi.org/10.1016/j.jinorgbio.2018.06.009.
- Komarnicka, U. K.; Kozieł, S.; Zabierowski, P.; Kruszyński, R.; Lesiów, M. K.; Tisato, F.; Porchia, M.; Kyzioł, A. Copper(I) Complexes with Phosphines P(p-OCH3-Ph)2CH2OH and P(p-OCH3-Ph)2CH2SarGly. Synthesis, Multimodal DNA Interactions, and Prooxidative and in Vitro Antiproliferative Activity. J. Inorg. Biochem. 2020, 203, id: 110926. DOI: https://doi.org/10.1016/j.jinorgbio.2019.110926.
- Westhues, N. F. Development of Molecular Transition-Metal Catalysts for the Reverse Water-Gas Shift Reaction and the Selective Transformation of Carbon Dioxide and Hydrogen to Formic Acid Esters and Methanol. Ph.D. Dissertation, RWTH Aachen University, Aachen, Germany, 2020.
- Petrov, K. A.; Parshina, V. A.; Orlov, B. A.; Tsypina, G. M. Properties of Phosphines. V. Reactions of Phosphines with Chloramines, Sulfenyl Chlorides, and Amines. Zh. Obshch. Khim. 1962, 32, 4017–4022.
- Kostyanovskii, R. G.; Él'natanov, Y. I.; Shikhaliev, S. M. Aminomethylation of Phosphines by Alkoxymethylamines and Diaminomethanes. Russ. Chem. Bull. 1979, 28, 1470–1474. DOI: https://doi.org/10.1007/BF00947322.
- Issleib, K.; Kümmel, R.; Oehme, H.; Meißner, I. Alkali‐Phosphorverbindungen und Ihr Reaktives Verhalten, LIX. Synthese und Reaktionsverhalten der 2‐Amino‐Äthylphosphine. Chem. Ber. 1968, 101, 3612–3618. DOI: https://doi.org/10.1002/cber.19681011035.
- Arbuzov, B. A.; Erastov, O. A.; Nikonov, G. N. Preparation and Some Properties of Diphenylboryloxymethyl(Methyl) Phenylphosphine. Russ. Chem. Bull. 1983, 32, 2287–2290. DOI: https://doi.org/10.1007/BF00954710.
- Maier, L.; Organische Phorsphorverbindungen, XXXV. Die α-Aminoalkylierung von Elementarem Weissem Phosphor und von Biphosphinen. Darstellung und Reaktionen von Dialkylaminomethyl-Substituierten Tertiären Phosphinoxiden. Helv. Chim. Acta 1968, 51, 1608–1616. DOI: https://doi.org/10.1002/hlca.19680510716.
- Maier, L.; Process for Preparing Nitrogen-Containing Tertiary Phosphines and Phosphine Oxides. U.S. Patent 3,553,265, Jan 5, 1971.
- Yan, P.; Hashimoto, Y. A Novel Reductive Coupling Reaction between Diphenylphosphine Sulfide and Formamides. Tetrahedron Lett. 2006, 47, 3467–3469. DOI: https://doi.org/10.1016/j.tetlet.2006.03.073.
- Brown, G. M. Synthesis and Screening of Ligands for Catalytic Olefin Oligomerisation Reactions. Ph.D. Dissertation, Loughborough University, Loughborough, UK, 2009.
- Kostyanovskii, R. G.; El'natanov, Y. I.; Shikhaliev, S. M. Synthesis of Aminomethylphosphines and Their Cleavage with Acid Chlorides to Acylphosphines. Russ. Chem. Bull. 1977, 26, 222–222. DOI: https://doi.org/10.1007/BF00921542.
- Kostyanovsky, R. G.; Voznesensky, V. N.; Kadorkina, G. K.; El'natanov, Y. I. Mass Spectrometry of Organic Compounds of the Group V Elements: VI - A New Type of Amine Fragmentation under Electron Impact. Org. Mass Spectrom. 1980, 15, 412–418. DOI: https://doi.org/10.1002/oms.1210150804.
- Lundberg, K. L.; Rowatt, R. J.; Miller, N. E. gem-Dibasic Ligands with Phosphorus, Sulfur, and Nitrogen Sites, and Some Borane Derivatives. Inorg. Chem. 1969, 8, 1336–1340. DOI: https://doi.org/10.1021/ic50076a027.
- Aguiar, A. M.; Hansen, K. C.; Mague, J. T. 3-Oxa-, Aza-, and Thioorganophosphonium Heterocyclics via α-Alkoxy, α-Dialkylamino, and α-Thioalkoxy Tertiary Phosphines. J. Org. Chem. 1967, 32, 2383–2387. DOI: https://doi.org/10.1021/jo01283a005.
- McEwen, W. E.; Smith, J. H.; Woo, E. J. Role of through Space 2p-3d Overlap in the Alkylation of (ω-N,N-Dimethylaminoalkyl)Diphenylphosphines and in the Alkaline Decomposition of Related Quaternary Phosphonium Salts. J. Am. Chem. Soc. 1980, 102, 2746–2751. DOI: https://doi.org/10.1021/ja00528a037.
- Abu-Gnim, C.; Amer, I. Phosphine Oxides as Ligands in the Hydroformylation Reaction. J. Organomet. Chem. 1996, 516, 235–243. DOI: https://doi.org/10.1016/0022-328X(96)06137-2.
- Kellner, K.; Hanke, W. Unsymmetrisch Substitutierte N,N-Bisphosphinomethyl- und N-Phosphinomethyl-N-Thiomethyl-α-Aminosäuren. J. Organomet. Chem. 1987, 326, C9–C12. DOI: https://doi.org/10.1016/0022-328X(87)80132-8.
- Lischewski, M.; Issleib, K.; Tille, H. Alkali-Phosphor Verbindungen und Ihr Reaktives Verhalten: LXVIII. Dialkylphosphino-Bis(Dimethylamino)Methane. J. Organomet. Chem. 1973, 54, 195–201. DOI: https://doi.org/10.1016/S0022-328X(00)85008-1.
- Issleib, K.; Lischewski, M. Alkali-Phosphor-Verbindungen und Ihr Reaktives Verhalten: LXVII. Bis(Diorganylphosphino)-Dimethylamino-Methane und Diäthylphosphino-Dimethylamino-Methoxy-Methane. J. Organomet. Chem. 1972, 46, 297–304. DOI: https://doi.org/10.1016/S0022-328X(00)88331-X.
- Song, H.-B.; Wang, Q.-M.; Zhang, Z.-Z.; Mak, T. C. W. Synthesis and Structural Characterization of Hetero-Binuclear Complexes Containing a Fe0→Mn+ Bond Bridged by a Non-Rigid P,N-Phosphine Ligand. J. Organomet. Chem. 2000, 605, 15–21. DOI: https://doi.org/10.1016/S0022-328X(00)00248-5.
- Płotek, M.; Starosta, R.; Komarnicka, U. K.; Skórska-Stania, A.; Jeżowska-Bojczuk, M.; Stochel, G.; Kyzioł, A. New Ruthenium(II) Coordination Compounds Possessing Bidentate Aminomethylphosphane Ligands: Synthesis, Characterization and Preliminary Biological Study in Vitro. Dalton Trans. 2015, 44, 13969–13978. DOI: https://doi.org/10.1039/C5DT01119A.
- Kuang, S.-M.; Zhang, Z.-Z.; Wang, Q.-G.; Mak, T. C. W. Synthesis of the New Polydentate Phosphine Ligand 1-[(Diphenylphosphino)Methyl]-4-(2-Pyridyl)Piperazine and Structural Characterization of Its Binuclear Silver(I) and Mononuclear Iron(0) Complexes. Inorg. Chem. 1998, 37, 6090–6092. DOI: https://doi.org/10.1021/ic9800482.
- Clarke, M. L.; Slawin, A. M. Z.; Wheatley, M. V.; Woollins, J. D. Synthesis and Structure of Novel Rhodium Complexes of Multi-Functionalised Amine-Phosphine Ligands. J. Chem. Soc, Dalton Trans. 2001, 3421–3429. DOI: https://doi.org/10.1039/b104523g.
- Ma, X.; Fu, X.; Li, L. Synthesis of New Type of Water-Soluble Hybrid Phosphine-Phosphonate Ligands. Synth. Commun. 2002, 32, 539–546. DOI: https://doi.org/10.1081/SCC-120002399.
- de Almeida, R. F. M.; Santos, T. C. B.; da Silva, L. C.; Suchodolski, J.; Krasowska, A.; Stokowa-Sołtys, K.; Puchalska, M.; Starosta, R. NBD Derived Diphenyl(Aminomethyl) Phosphane – A New Fluorescent Dye for Imaging of Low pH Regions and Lipid Membranes in Living Cells. Dyes Pigm. 2021, 184, 108771. DOI: https://doi.org/10.1016/j.dyepig.2020.108771.
- Kostyanovskii, R. G.; Él'natanov, Y. I.; Shikhaliev, S. M. Optically Active Aminomethylphosphines. Russ. Chem. Bull. 1978, 27, 845–845. DOI: https://doi.org/10.1007/BF00925330.
- Bykowska, A.; Starosta, R.; Brzuszkiewicz, A.; Bażanów, B.; Florek, M.; Jackulak, N.; Król, J.; Grzesiak, J.; Kaliński, K.; Jeżowska-Bojczuk, M. Synthesis, Properties and Biological Activity of a Novel Phosphines Ligand Derived from Ciprofloxacin. Polyhedron 2013, 60, 23–29. DOI: https://doi.org/10.1016/j.poly.2013.04.059.
- Bykowska, A.; Starosta, R.; Komarnicka, U. K.; Ciunik, Z.; Kyzioł, A.; Guz-Regner, K.; Bugla-Płoskońska, G.; Jeżowska-Bojczuk, M. Phosphine Derivatives of Ciprofloxacin and Norfloxacin, a New Class of Potential Therapeutic Agents. New J. Chem. 2014, 38, 1062–1071. DOI: https://doi.org/10.1039/c3nj01243c.
- Komarnicka, U. K.; Starosta, R.; Guz-Regner, K.; Bugla-Płoskońska, G.; Kyzioł, A.; Jeżowska-Bojczuk, M. Phosphine Derivatives of Sparfloxacin – Synthesis, Structures and in Vitro Activity. J. Mol. Struct. 2015, 1096, 55–63. DOI: https://doi.org/10.1016/j.molstruc.2015.04.044.
- Komarnicka, U. K.; Starosta, R.; Kyzioł, A.; Płotek, M.; Puchalska, M.; Jeżowska-Bojczuk, M. New Copper(I) Complexes Bearing Lomefloxacin Motif: Spectroscopic Properties, in Vitro Cytotoxicity and Interactions with DNA and Human Serum albumin. J. Inorg. Biochem. 2016, 165, 25–35. DOI: https://doi.org/10.1016/j.jinorgbio.2016.09.015.
- Almeida, R. F. M.; Santos, F. C.; Marycz, K.; Alicka, M.; Krasowska, A.; Suchodolski, J.; Panek, J. J.; Jezierska, A.; Starosta, R. New Diphenylphosphane Derivatives of Ketoconazole Are Promising Antifungal Agents. Sci. Rep. 2019, 9, 16214. DOI: https://doi.org/10.1038/s41598-019-52525-7.
- Starosta, R.; Almeida, R. F. M.; Puchalska, M.; Białońska, A.; Panek, J. J.; Jezierska, A.; Szmigiel, I.; Suchodolski, J.; Krasowska, A. New Anticandidal Cu(I) Complexes with Neocuproine and Ketoconazole Derived Diphenyl(Aminomethyl) Phosphane: Luminescence Properties for Detection in Fungal Cells. Dalton Trans. 2020, 49, 8528–8539. DOI: https://doi.org/10.1039/D0DT01162B.
- Hazari, A.; Labinger, J. A.; Bercaw, J. E. A Versatile Ligand Platform That Supports Lewis Acid Promoted Migratory Insertion. Angew. Chem. Int. Ed. 2012, 51, 8268–8271. DOI: https://doi.org/10.1002/anie.201203264.
- McLain, S. J. Organometallic Crown Ethers. 1. Metal-Acyl Binding to a Crown Ether-Held Cation. J. Am. Chem. Soc. 1983, 105, 6355–6357. DOI: https://doi.org/10.1021/ja00358a051.
- McLain, S. J. Organometallic Crown Ethers. 2. Syntheses of Phosphino Aza Crown Ether Ligands. Inorg. Chem. 1986, 25, 3124–3127. DOI: https://doi.org/10.1021/ic00238a005.
- Berdini, V.; Bassetti, M.; Mancini, G.; Mandolini, L.; Monti, D. Metal Ion Complexation in Organometallic Crown Ethers: Structural and Rate Effects on the Migratory Insertion of Carbon Monoxide in Indenyl and Cyclopentadienyl Iron (II) Complexes. J. Organomet. Chem. 1998, 551, 331–338. DOI: https://doi.org/10.1016/S0022-328X(97)00521-4.
- Pap, L. G.; Arulsamy, N.; Hulley, E. B. Tridentate Phosphine Ligands Bearing Aza-Crown Ether Lariats. Polyhedron 2018, 141, 385–392. DOI: https://doi.org/10.1016/j.poly.2017.11.012.
- Tzschach, A.; Kellner, K. Organoarsen-Verbindungen. XXIII. Darstellung Imidomethylsubstituierter Tertiärer Phosphine und Arsine. J. Prakt. Chem. 1974, 316, 851–856. DOI: https://doi.org/10.1002/prac.19743160518.
- Rodríguez, L. I.; Roth, T.; Fillol, J. L.; Wadepohl, H.; Gade, L. H. The More Gold-the More Enantioselective: Cyclohydroaminations of γ-Allenyl Sulfonamides With Mono-, bis-, and Trisphospholane Gold(I) Catalysts. Chemistry 2012, 18, 3721–3728. DOI: https://doi.org/10.1002/chem.201103140.
- Fawcett, J.; Hoye, P. A. T.; Kemmitt, R. D. W.; Law, D. J.; Russell, D. R. Synthesis of Bis(Phosphinomethyl)Amines via Bis(Hydroxymethyl)Phosphonium Salts. Isolation of 9,9-Bis(Hydroxymethyl)-9-Phosphoniabicyclo[3.3.1]Nonane Hydrogensulfate and Chloride Salts, and the Crystal Structures of [PPh2(CH2OH)2]+Cl– and [(C6H11)2PCH2]2NCHMePh. J. Chem. Soc., Dalton Trans. 1993, 2563–2568. DOI: https://doi.org/10.1039/DT9930002563.
- Naziruddin, A. R.; Hepp, A.; Pape, T.; Hahn, F. E. Synthesis of Rhodium(I) Complexes Bearing Bidentate NH,NR-NHC/Phosphine Ligands. Organometallics 2011, 30, 5859–5866. DOI: https://doi.org/10.1021/om200689r.
- Hahn, F. E.; Naziruddin, A. R.; Hepp, A.; Pape, T. Synthesis, Characterization, and H-Bonding Abilities of Ruthenium(II) Complexes Bearing Bidentate NR,NH-Carbene/Phosphine Ligands. Organometallics 2010, 29, 5283–5288. DOI: https://doi.org/10.1021/om100388w.
- Guerrero, M.; Muñoz, S.; Ros, J.; Calvet, T.; Font-Bardía, M.; Pons, J. New N-Pyrazole, P-Phosphine Hybrid Ligands and Their Reactivity towards Pd(II): X-Ray Crystal Structures of Complexes with [PdCl2(N,P)] Core. J. Organomet. Chem. 2015, 799-800, 257–264. DOI: https://doi.org/10.1016/j.jorganchem.2015.10.007.
- Junges, C. H.; Dresch, L. C.; Costa, M. T.; Tirloni, B.; Casagrande, O. L.; Stieler, R. Pyrazolyl-Phosphinoyl Nickel(II) Complexes: Synthesis, Characterization and Ethylene Dimerization Studies. Appl. Organometal. Chem. 2019, 33, id: e4887. DOI: https://doi.org/10.1002/aoc.4887.
- Salem, H.; Schmitt, M.; Herrlich, U.; Kühnel, E.; Brill, M.; Nägele, P.; Bogado, A. L.; Rominger, F.; Hofmann, P. Bulky N-Phosphinomethyl-Functionalized N-Heterocyclic Carbene Chelate Ligands: Synthesis, Molecular Geometry, Electronic Structure, and Their Ruthenium Alkylidene Complexes. Organometallics 2013, 32, 29–46. DOI: https://doi.org/10.1021/om300487r.
- Takahashi, K.; Cho, K.; Iwai, A.; Ito, T.; Iwasawa, N. Development of N-Phosphinomethyl-Substituted NHC-Nickel(0) Complexes as Robust Catalysts for Acrylate Salt Synthesis from Ethylene and CO2. Chem. Eur. J. 2019, 25, 13504–13508. DOI: https://doi.org/10.1002/chem.201903625.
- Buhaibeh, R.; Duhayon, C.; Valyaev, D. A.; Sortais, J.-B.; Canac, Y. Cationic PCP and PCN NHC Core Pincer-Type Mn(I) Complexes: From Synthesis to Catalysis. Organometallics 2021, 40, 231–241. DOI: https://doi.org/10.1021/acs.organomet.0c00717.
- Danopoulos, A. A.; Tsoureas, N.; Macgregor, S. A.; Smith, C. Phosphine- and Pyridine-Functionalized N-Heterocyclic Carbene Methyl and Allyl Complexes of Palladium. Unexpected Regiospecificity of the Protonation Reaction of the Dimethyl Complexes. Organometallics 2007, 26, 253–263. DOI: https://doi.org/10.1021/om0608408.
- Song, G.; Wang, X.; Li, Y.; Li, X. Iridium Abnormal N-Heterocyclic Carbene Hydrides via Highly Selective C-H Activation. Organometallics 2008, 27, 1187–1192. DOI: https://doi.org/10.1021/om7011216.
- Schuster, E. M.; Botoshansky, M.; Gandelman, M. Pincer Click Ligands. Angew. Chem. Int. Ed. 2008, 47, 4555–4558. DOI: https://doi.org/10.1002/anie.200800123.
- Schuster, E. M.; Nisnevich, G.; Botoshansky, M.; Gandelman, M. Synthesis of Novel Bulky, Electron-Rich Propargyl and Azidomethyl Dialkyl Phosphines and Their Use in the Preparation of Pincer Click Ligands. Organometallics 2009, 28, 5025–5031. DOI: https://doi.org/10.1021/om900545s.
- Detz, R. J.; Heras, S. A.; de Gelder, R.; van Leeuwen, P. W. N. M.; Hiemstra, H.; Reek, J. N. H.; van Maarseveen, J. H. “Clickphine”: A Novel and Highly Versatile P,N Ligand Class via Click Chemistry. Org. Lett. 2006, 8, 3227–3230. DOI: https://doi.org/10.1021/ol061015q.
- Liu, Y.; Fan, X.; Tian, R.; Duan, Z. FeCl2 Catalyzed Three-Component Reactions of Phospholes, Pyrrolidine, and Ketones (Aldehydes): Chemoselective Synthesis of 1-Phosphafulvenes. Org. Lett. 2021, 23, 2943–2947. DOI: https://doi.org/10.1021/acs.orglett.1c00602.
- Angurell, I.; Turrin, C.-O.; Laurent, R.; Maraval, V.; Servin, P.; Rossell, O.; Seco, M.; Caminade, A.-M.; Majoral, J.-P. Decorating Step-by-Step and Independently the Surface and the Core of Dendrons. J. Organomet. Chem. 2007, 692, 1928–1939. DOI: https://doi.org/10.1016/j.jorganchem.2007.01.001.
- Oehme, H.; Leissring, E.; Zschunke, A. Synthese und Stereochemie der 1-Amino- und 1-Phenylamino-1,3-Azaphospholan-5-One. Phosphorus Sulfur Silicon Relat. Elem. 1978, 4, 59–66. DOI: https://doi.org/10.1080/03086647808079966.
- Serindag, O. The Synthesis of Some Aminobis (Methylphosphines) and Their Transition Metal Complexes. Ph.D. Dissertation, University of Leicester, Leicester, UK, 1993.
- Clark, H. Synthetic Approaches towards Dendrimeric Catalysts. Ph.D. Dissertation, University of Ottawa, Ottawa, Canada, 2001.
- Elsegood, M. R. J.; Lake, A. J.; Mortimer, R. J.; Smith, M. B.; Weaver, G. W. Synthesis, Coordination Studies and Redox Properties of a Novel Ditertiary Phosphine Bearing Two Ferrocenyl Groups. J. Organomet. Chem. 2008, 693, 2317–2326. DOI: https://doi.org/10.1016/j.jorganchem.2008.04.005.
- Elsegood, M. R. J.; Lake, A. J.; Mortimer, R. J.; Smith, M. B.; Weaver, G. W. A New Tris(Ferrocenylamine) Ditertiary Phosphine: Synthesis and Co-Ordination Studies. J. Organomet. Chem. 2010, 695, 1838–1842. DOI: https://doi.org/10.1016/j.jorganchem.2010.04.012.
- Xu, F.-B.; Li, Q.-S.; Zeng, X.-S.; Leng, X.-B.; Zhang, Z.-Z. Bimetallocyclophanes Formed by the π − π Stacking Interaction Approach and Fluorescent Chemosensing Behavior. Organometallics 2004, 23, 632–634. DOI: https://doi.org/10.1021/om0340037.
- Li, Q.-S.; Wan, C.-Q.; Xu, F.-B.; Song, H.-B.; Zhang, Z.-Z. Synthesis of a Novel Pyridine-Diamino Bridged Diphosphine Ligand and Its Macrocyclic Metal Complexes. Inorg. Chim. Acta 2005, 358, 2283–2291. DOI: https://doi.org/10.1016/j.ica.2005.01.008.
- Diehl, E.; Brückner, R. Turning the Nitrogen Atoms of an Ar2P − CH2−N − N−CH2−PAr2 Motif into Uniquely Configured Stereocenters: A Novel Diphosphane Design for Asymmetric Catalysis. Chem. Eur. J. 2018, 24, 3429–3433. DOI: https://doi.org/10.1002/chem.201706160.
- Balch, A. L.; Rowley, S. P. Solubilizing the Thallium-Platinum Unit of Tl2Pt(CN)4. Preparation and Use of a New Crown Ether/Phosphine Hybrid Ligand for Linking Main-Group and Transition-Metal Ions. J. Am. Chem. Soc. 1990, 112, 6139–6140. DOI: https://doi.org/10.1021/ja00172a046.
- Hope, H.; Viggiano, M.; Moezzi, B.; Power, P. P. Syntheses and X-Ray Crystal Structures of Two New Classes of Macrocyclic Ligands Having Both Phosphorus and Nitrogen Donor Atoms. Inorg. Chem. 1984, 23, 2550–2552. DOI: https://doi.org/10.1021/ic00184a035.
- Subramaniyan, V.; Dutta, B.; Govindaraj, A.; Mani, G. Facile Synthesis of Pd(II) and Ni(II) Pincer Carbene Complexes by the Double C-H Bond Activation of a New Hexahydropyrimidine-Based Bis(phosphine): Catalysis of C-N Couplings. Dalton Trans. 2019, 48, 7203–7210. DOI: https://doi.org/10.1039/C8DT03413C.
- Hill, A. F.; McQueen, C. M. A. N-Heterocyclic Pincer Carbene Complexes via Double C–H Activation. Organometallics 2012, 31, 8051–8054. DOI: https://doi.org/10.1021/om300897w.
- Langbein, S.; Wadepohl, H.; Gade, L. H. Ditopic N-Heterocyclic Pincer Carbene Complexes Containing a Perylene Backbone. Organometallics 2016, 35, 809–815. DOI: https://doi.org/10.1021/acs.organomet.6b00049.
- Plikhta, A.; Pöthig, A.; Herdtweck, E.; Rieger, B. Toward New Organometallic Architectures: Synthesis of Carbene-Centered Rhodium and Palladium Bisphosphine Complexes. Stability and Reactivity of [PCBImPRh(L)][PF6] Pincers. Inorg. Chem. 2015, 54, 9517–9528. DOI: https://doi.org/10.1021/acs.inorgchem.5b01428.
- Priya, S.; Balakrishna, M. S.; Mobin, S. M. Reactions of Aminophosphines and Aminobis(Phosphines) with Aldehydes and Ketones: Coordination Complexes of the Resultant Aminobis(Alkylphosphineoxides) with Cobalt, Uranium, Thorium and Gadolinium Salts: Crystal and Molecular Structures of Ph2P(O)CH(C6H4OH-o)N(H)Ph, Ph2P(O)CH(OH) C6H4OH-o and Ph2P(O)N(H)Ph. Polyhedron 2005, 24, 1641–1650. DOI: https://doi.org/10.1016/j.poly.2005.04.036.
- Christensen, C. A.; Meldal, M. Efficient Solid-Phase Synthesis of Peptide-Based Phosphine Ligands: Towards Combinatorial Libraries of Selective Transition Metal Catalysts. Chemistry 2005, 11, 4121–4131. DOI: https://doi.org/10.1002/chem.200500105.
- Slany, M.; Caminade, A.-M.; Majoral, J. P. Specific Functionalization on the Surface of Dendrimers. Tetrahedron Lett. 1996, 37, 9053–9056. DOI: https://doi.org/10.1016/S0040-4039(96)02123-5.
- Lartigue, M.-L.; Caminade, A.-M.; Majoral, J. P. Chiroptical Properties of Dendrimers with Stereogenic End Groups. Tetrahedron Asymm. 1997, 8, 2697–2708. DOI: https://doi.org/10.1016/S0957-4166(97)00304-2.
- Slany, M.; Bardaji, M.; Casanove, M.-J.; Caminade, A.-M.; Majoral, J.-P.; Chaudret, B. Dendrimer Surface Chemistry. Facile Route to Polyphosphines and Their Gold Complexes. J. Am. Chem. Soc. 1995, 117, 9764–9765. DOI: https://doi.org/10.1021/ja00143a023.
- Slany, M.; Bardaji, M.; Caminade, A.-M.; Chaudret, B.; Majoral, J. P. Versatile Complexation Ability of Very Large Phosphino-Terminated Dendrimers. Inorg. Chem. 1997, 36, 1939–1945. DOI: https://doi.org/10.1021/ic961258m.
- Maraval, V.; Sebastian, R. M.; Ben, F.; Laurent, R.; Caminade, A. M.; Majoral, J. P. Varying Topology of Dendrimers − a New Approach toward the Synthesis of Di‐Block Dendrimers. Eur. J. Inorg. Chem. 2001, 1681–1691. DOI: https://doi.org/10.1002/1099-0682(200107)2001:7 < 1681::AID-EJIC1681 > 3.0.CO;2-T.
- Tolentino, D. R.; Neale, S. E.; Isaac, C. J.; Macgregor, S. A.; Whittlesey, M. K.; Jazzar, R.; Bertrand, G. Reductive Elimination at Carbon under Steric Control. J. Am. Chem. Soc. 2019, 141, 9823–9826. DOI: https://doi.org/10.1021/jacs.9b04957.
- Blackaby, W. J. M.; Neale, S. E.; Isaac, C. J.; Sabater, S.; Macgregor, S. A.; Whittlesey, M. K. N-Heterocyclic Carbene Non-Innocence in the Catalytic Hydrophosphination of Alkynes. ChemCatChem 2019, 11, 1893–1897. DOI: https://doi.org/10.1002/cctc.201900220.
- Holthausen, M. H.; Mahdi, T.; Schlepphorst, C.; Hounjet, L. J.; Weigand, J. J.; Stephan, D. W. Frustrated Lewis Pair-Mediated C-O or C-H Bond Activation of Ethers. Chem. Commun. 2014, 50, 10038–10040. DOI: https://doi.org/10.1039/c4cc01922a.
- Takata, T.; Nishikawa, D.; Hirano, K.; Miura, M. Synthesis of α-Aminophosphines by Copper-Catalyzed Regioselective Hydroamination of Vinylphosphines. Chemistry 2018, 24, 10975–10978. DOI: https://doi.org/10.1002/chem.201802491.
- Oehme, H.; Thamm, R. Synthese und Reaktionsverhalten der (3-Aminopropyl)-Phenylphosphine. J. Prakt. Chem. 1973, 315, 526–538. DOI: https://doi.org/10.1002/prac.19733150320.
- Andrieu, J.; Richard, P.; Camus, J.-M.; Poli, R. Synthesis, Coordination to Rh(I), and Hydroformylation Catalysis of New β-aminophosphines Bearing a Dangling Nitrogen Group: An Unusual Inversion of a Rh-coordinated P Center. Inorg. Chem. 2002, 41, 3876–3885. DOI: https://doi.org/10.1021/ic011035i.
- Basvani, K. R.; Kindermann, M. K.; Frauendorf, H.; Schulzke, C.; Jones, P. G.; Heinicke, J. W. 3-Phenylphosphaprolines – Synthesis, Structure and Properties of Heterocyclic α-Phosphanyl Amino Acids. Polyhedron 2017, 130, 195–204. DOI: https://doi.org/10.1016/j.poly.2017.04.014.
- Basvani, K. R. Novel Cyclic α-Phosphino-α-Amino Acids and α-Phosphonium Glycolates, P,O- Ligands and Nickel Complexes (Syntheses, Structural Characterization, Properties and Use in Catalysis). Ph.D. Dissertation, University of Greifswald, Greifswald, Germany, 2010.
- Heinicke, J.; Basvani, K. R.; Jones, P. G. α-Phosphino Amino Acids: Synthesis, Structure, and Reactivity of Phosphaprolines. Phosphorus Sulfur Silicon Relat. Elem. 2011, 186, 678–682. DOI: https://doi.org/10.1080/10426507.2010.515956.
- Roberts, R. M.; DeWolfe, R. H. Ortho Esters, Imidic Esters and Amidines. IV. The Mechanism of the Reaction of Aniline with Ethyl Orthoformate. J. Am. Chem. Soc. 1954, 76, 2411–2414. DOI: https://doi.org/10.1021/ja01638a033.
- DeWolfe, R. H. Reactions of Aromatic Amines with Aliphatic Ortho Esters. A Convenient Synthesis of Alkyl N-Arylimidic Esters. J. Org. Chem. 1962, 27, 490–493. DOI: https://doi.org/10.1021/jo01049a036.
- Swaringen, R. A.; Eaddy, J. F.; Henderson, T. R. Reaction of Ortho Esters with Secondary Amines. J. Org. Chem. 1980, 45, 3986–3989. DOI: https://doi.org/10.1021/jo01308a007.
- Saba, S.; Ciaccio, J. A. Reaction of Orthoesters with Amine Hydrochlorides: An Introductory Organic Lab Experiment Combining Synthesis, Spectral Analysis, and Mechanistic Discovery. J. Chem. Educ. 2016, 93, 945–948. DOI: https://doi.org/10.1021/acs.jchemed.5b00782.
- Lightburn, T. E.; Dombrowski, M. T.; Tan, K. L. Catalytic Scaffolding Ligands: An Efficient Strategy for Directing Reactions. J. Am. Chem. Soc. 2008, 130, 9210–9211. DOI: https://doi.org/10.1021/ja803011d.
- Worthy, A. D.; Tan, K. (2S,3R)-2-Isopropoxy-1-methyl-3-phenyl-2,3-dihydro-1H-benzo[d][1,3]azaphosphole. In Encyclopedia of Reagents for Organic Synthesis; John Wiley & Sons, 2013, pp. 1–3. DOI: https://doi.org/10.1002/047084289X.rn01580.
- Sun, X.; Frimpong, K.; Tan, K. L. Synthesis of Quaternary Carbon Centers via Hydroformylation. J. Am. Chem. Soc. 2010, 132, 11841–11843. DOI: https://doi.org/10.1021/ja1036226.
- Lightburn, T. E.; Paolis, O. A. D.; Cheng, K. H.; Tan, K. L. Regioselective Hydroformylation of Allylic Alcohols. Org. Lett. 2011, 13, 2686–2689. DOI: https://doi.org/10.1021/ol200782d.
- Tan, K. L. Induced Intramolecularity: An Effective Strategy in Catalysis. ACS Catal. 2011, 1, 877–886. DOI: https://doi.org/10.1021/cs2002302.
- Worthy, A. D.; Gagnon, M. M.; Dombrowski, M. T.; Tan, K. L. Regioselective Hydroformylation of Sulfonamides Using a Scaffolding Ligand. Org. Lett. 2009, 11, 2764–2767. DOI: https://doi.org/10.1021/ol900921e.
- Worthy, A. D.; Joe, C. L.; Lightburn, T. E.; Tan, K. L. Application of a Chiral Scaffolding Ligand in Catalytic Enantioselective Hydroformylation. J. Am. Chem. Soc. 2010, 132, 14757–14759. DOI: https://doi.org/10.1021/ja107433h.
- Joe, C. L.; Tan, K. L. Enantioselective Hydroformylation of Aniline Derivatives. J. Org. Chem. 2011, 76, 7590–7596. DOI: https://doi.org/10.1021/jo201328d.
- Aluri, B. R.; Ghalib, M.; Jones, P. G.; Frauendorf, H.; Heinicke, J. W. Synthesis of N,P-Disecondary o-Arylphosphanylanilines via o-R1NHC6H4P(R)O2Et Precursors and Preliminary Study of Cyclocondensations with (EtO)3CH/NH4PF6. Eur. J. Inorg. Chem. 2020, 2020, 182–190. DOI: https://doi.org/10.1002/ejic.201901069.
- Niaz, B.; Aluri, B. R.; Jones, P. G.; Heinicke, J. W. π Excess σ2P = C–N–Heterocycles: Catalytic P-Arylation and Alkylation of N-Alkyl-1,3-Benzazaphospholes and Isolation of P,N-Disubstituted Dihydrobenzazaphosphole P-Oxides. Eur. J. Inorg. Chem. 2015, 3995–4005. DOI: https://doi.org/10.1002/ejic.201500532.
- Aluri, B. R.; Kindermann, M. K.; Jones, P. G.; Heinicke, J. Sterically and Polarity-Controlled Reactions of tBuLi with P-CH-NR Heterocycles: Novel Heterocyclic P- and P,O-Ligands and Preliminary Tests in Transition-Metal Catalysis. Chem. Eur. J. 2008, 14, 4328–4335. DOI: https://doi.org/10.1002/chem.200702016.
- Aluri, B. R.; Ghalib, M.; Kindermann, M. K.; Jones, P. G.; Heinicke, J. W. π-Excess Aromatic σ2P Ligands: Formation of a Heterocyclic 1,2-Diphosphine by the Addition of tBuLi and Subsequent Inverse Addition of the Product at the P = C Bonds of Two Molecules of 1-Neopentyl-1,3-Benzazaphosphole. Heteroatom Chem. 2015, 26, 426–435. DOI: https://doi.org/10.1002/hc.21277.
- Ghalib, M.; Jones, P. G.; Heinicke, J. W. [(Lithiumbenzazaphospholine-2-Carboxylate-κP)Rh(COD)Cl] — the First Structurally Characterized Phosphinoalkanoate RhCl Complex with Rh–Cl…Alkali Metal Interactions. Inorg. Chem. Commun. 2015, 57, 66–68. DOI: https://doi.org/10.1016/j.inoche.2015.05.006.
- Heinicke, J. W. Electron-Rich Aromatic 1,3-Heterophospholes – Recent Syntheses and Impact of High Electron Density at σ2P on the Reactivity. Eur. J. Inorg. Chem. 2016, 575–594. DOI: https://doi.org/10.1002/ejic.201500941.
- Muller, G.; Sainz, D. Synthesis of Monohydroxy -Methyl- and -Ethyl-Phosphines PPh2CHROH. J. Organomet. Chem. 1995, 495, 103–111. DOI: https://doi.org/10.1016/0022-328X(95)05425-O.
- Moiseev, D. V.; Patrick, B. O.; James, B. R. New Tertiary Phosphines from Cinnamaldehydes and Diphenylphosphine. Inorg. Chem. 2007, 46, 11467–11474. DOI: https://doi.org/10.1021/ic701597g.
- Moiseev, D. V.; Marcazzan, P.; James, B. R. Reversible Decomposition of Mono(α-Hydroxy)Phosphines and Their Reaction with α,β-Unsaturated Aldehydes. Can. J. Chem. 2009, 87, 582–590. DOI: https://doi.org/10.1139/V09-021.
- Hoffmann, H.; Förster, H. Darstellung von α-Aminophosphonsäureestern und Verwandten Verbindungen. Monatsh. Chem. 1968, 99, 380–388. DOI: https://doi.org/10.1007/BF00908943.
- Lange, D. Elektronische und Sterische Differenzierung in Enantioselektiven Katalysatoren und Reagenzien. Ph.D. Dissertation, Universität zu Köln, Köln, Germany, 2007.
- Romanov, G. V.; Ryzhikova, T. Y.; Pudovik, A. N. Tertiary Aminotrichloroethylphosphines and Their Oxides. Russ. Chem. Bull. 1984, 33, 1311–1312. DOI: https://doi.org/10.1007/BF00949010.
- Ben-Aroya, B. B.-N.; Portnoy, M. Preparation of α-Aminophosphines on Solid Support: Model Studies and Parallel Synthesis. Tetrahedron 2002, 58, 5147–5158. DOI: https://doi.org/10.1016/S0040-4020(02)00471-4.
- Wu, L.; Annibale, V. T.; Jiao, H.; Brookfield, A.; Collison, D.; Manners, I. Homo- and Heterodehydrocoupling of Phosphines Mediated by Alkali Metal Catalysts. Nat. Commun. 2019, 10, id: 2786 DOI: https://doi.org/10.1038/s41467-019-09832-4.
- Kellner, K.; Schultz, H. J.; Tzschach, A. Synthese und Reaktionsverhalten von α‐Arylsulfonainido‐Benzylphosphinen und ‐Arsinen. Z Chem. 2010, 20, 152–152. DOI: https://doi.org/10.1002/zfch.19800200420.
- Pudovik, A. N.; Romanov, G. V.; Karelov, A. A.; Pozhidaev, V. M.; Stepanova, T. Y. Interaction of Diphenylphosphine and Diphenylphosphinic Acid with Azomethines. Zh. Obshch. Khim. 1981, 51, 2407–2410.
- Bar-Nir, B. B.-A.; Portnoy, M. Addition of Borane-Protected Secondary Phosphines to Imines. A Route to Protected Mono-N-Substituted-α-Aminophosphines. Tetrahedron Lett. 2000, 41, 6143–6147. DOI: https://doi.org/10.1016/S0040-4039(00)00993-X.
- Andújar Sánchez, C. M. Aplicaciones Sintéticas de Aniones de Complejos Fosfina Borano y Fosforil Fosfacenos. Ph.D. Dissertation, University of Almería, Almería, Spain, 2004.
- Du, L.-Z.; Gong, J.-F.; Zhu, Y.; Wu, Y.-J.; Song, M.-P. Synthesis, Characterization and the Crystal Structures of Novel Achiral and Chiral α-Ferrocenyl α-Aminophosphine Oxides. Inorg. Chem. Commun. 2006, 9, 529–532. DOI: https://doi.org/10.1016/j.inoche.2006.02.027.
- Couret, C.; Couret, F.; Satgé, J.; Escudié, J. Réactivité Des Silyl- et Germylphosphines Vis-à-Vis de Divers Composés à Insaturation C = N: Imines, α-Diimines, N-Acylimines et Cétènimines. Helv. Chim. Acta 1975, 58, 1316–1323. DOI: https://doi.org/10.1002/hlca.19750580510.
- Huang, M.; Li, C.; Huang, J.; Duan, W.-L.; Xu, S. Palladium-Catalyzed Asymmetric Addition of Diarylphosphines to N-Tosylimines. Chem. Commun. 2012, 48, 11148–11150. DOI: https://doi.org/10.1039/C2CC35563A.
- Andrieu, J.; Baldoli, C.; Maiorana, S.; Poli, R.; Richard, P. Chiral α‐P,N Ligands from a Diastereoselective Ph2PH Addition to (η6‐Benzaldimine)Tricarbonylchromium Complexes. Eur. J. Org. Chem. 1999, 3095–3097. DOI: https://doi.org/10.1002/(SICI)1099-0690(199911)1999:11 < 3095::AID-EJOC3095 > 3.0.CO;2-Q.
- Oehme, H.; Issleib, K.; Leissring, E. Synthese und Reaktionsverhalten der 1,3-Azaphospholan-5-One. Phosphorus 1973, 3, 159–163.
- Issleib, K.; Malotki, P. Alkali-Phosphor Verbindungen und Ihr Reaktives Verhalten, LXXI. Synthese und Reaktionsverhalten von (3-Oxa-Alkyl)-Organophosphinen. Phosphorus 1973, 3, 141–152.
- Barluenga, J.; Bayón, A. M.; Asensio, G. Monoalkylation of Primary Aromatic Amines via N-(Alkoxymethyl)Aryl Amines. Evidence for the Formation of Stable Monomeric Methyleneamines. J. Chem. Soc., Chem. Commun. 1983, 1109–1110. DOI: https://doi.org/10.1039/C39830001109.
- Barluenga, J.; Bayón, A. M.; Campos, P.; Asensio, G.; Gonzalez-Nuñez, E.; Molina, Y. Preparation of N,O-Aminals as Synthetic Equivalents of H2C = NAr and (H2C = NHAr)+ Ions: Neutral- and Acid-Promoted Transformations. J. Chem. Soc., Perkin Trans. 1 1988, 1631–1636. DOI: https://doi.org/10.1039/P19880001631.
- Barluenga, J.; Campos, P. J.; Canal, G.; Asensio, G. Nucleophilic Additions of Phosphorus Compounds to Aromatic Methyleneamines. Synlett 1990, 261–262. DOI: https://doi.org/10.1055/s-1990-21056.
- Lindner, E.; Mohr, M.; Nachtigal, C.; Fawzi, R.; Henkel, G. Preparation, Properties and Reactions of Metal-Containing Heterocycles: Part C: Tetraazatetraphosphadimolybdacyclophanes: Synthesis, Isolation, Characterization, and X-Ray Crystal Structures. J. Organomet. Chem 2000, 595, 166–177. DOI: https://doi.org/10.1016/S0022-328X(99)00587-2.
- Durran, S. E.; Smith, M. B.; Slawin, A. M. Z.; Gelbrich, T.; Hursthouse, M. B.; Light, M. E. Synthesis and Coordination Studies of New Aminoalcohol Functionalized Tertiary Phosphines. Can. J. Chem. 2001, 79, 780–791. DOI: https://doi.org/10.1139/v01-037.
- Cao, B.; Elsegood, M. R. J.; Lastra-Calvo, N.; Smith, M. B. New (Aminomethyl)Phosphines via Selective Hydrophosphination and/or Phosphorus Based Mannich Condensation Reactions. J. Organomet. Chem. 2017, 853, 159–167. DOI: https://doi.org/10.1016/j.jorganchem.2017.10.029.
- Zhang, Q.; Aucott, S. M.; Slawin, A. M. Z.; Woollins, J. D. Synthesis and Coordination Chemistry of the New Unsymmetrical Ligand Ph2PCH2NHC6H4PPh2. Eur. J. Inorg. Chem. 2002, 1635–1646. DOI: https://doi.org/10.1002/1099-0682(200207)2002:7 < 1635::AID-EJIC1635 > 3.0.CO;2-B.
- Smith, M. B.; Elsegood, M. R. J. Mannich-Based Condensation Reactions as a Practical Route to New Aminocarboxylic Acid Tertiary Phosphines. Tetrahedron Lett. 2002, 43, 1299–1301. DOI: https://doi.org/10.1016/S0040-4039(01)02361-9.
- Elsegood, M. R. J.; Karakus, M.; Noble, T. A.; Smith, M. B. Synthesis and Characterization of a New Dinuclear Ruthenium(II) Complex with a Bridging P/S-Ligand. Phosphorus Sulfur Silicon Relat. Elem. 2019, 194, 349–350. DOI: https://doi.org/10.1080/10426507.2018.1542396.
- Payet, E.; Auffrant, A.; Le Goff, X. F.; Le Floch, P. Phosphine- and Thiophosphorane-Amine Ligands: Lithiation and Coordination to Rh(I). J. Organomet. Chem. 2010, 695, 1499–1506. DOI: https://doi.org/10.1016/j.jorganchem.2010.03.006.
- Blann, K.; Bollmann, A.; Brown, G. M.; Dixon, J. T.; Elsegood, M. R. J.; Raw, C. R.; Smith, M. B.; Tenza, K.; Willemse, J. A.; Zweni, P. Ethylene Oligomerisation Chromium Catalysts with Unsymmetrical PCNP Ligands. Dalton Trans. 2021, 50, 4345–4354. DOI: https://doi.org/10.1039/D1DT00287B.
- Clarke, M. L.; Cole-Hamilton, D. J.; Foster, D. F.; Slawin, A. M. Z.; Woollins, J. D. Co-Ordination Chemistry and Metal Catalysed Carbonylation Reactions Using 8-(Diphenylphosphino)Methylaminoquinoline: A Ligand That Displays Monodentate, Bidentate and Tridentate Co-Ordination Modes. J. Chem. Soc, Dalton Trans. 2002, 1618–1624. DOI: https://doi.org/10.1039/b200401a.
- Durran, S. E.; Smith, M. B.; Slawin, A. M. Z.; Steed, J. W. The Synthesis and Co-Ordination Chemistry of New Functionalised Pyridylphosphines Derived from Ph2PCH2OH. J. Chem. Soc, Dalton Trans. 2000, 2771–2778. DOI: https://doi.org/10.1039/b003759l.
- Penney, M. K.; Potter, C.; Burroughs, M. A.; Klausmeyer, K. K. Silver Coordination Complexes of 2-(Diphenylphosphinomethyl) Aminopyridine with Weakly Interacting Counterions. Polyhedron 2015, 102, 207–215. DOI: https://doi.org/10.1016/j.poly.2015.09.048.
- Coles, S. J.; Durran, S. E.; Hursthouse, M. B.; Slawin, A. M. Z.; Smith, M. B. Late Transition Metal Complexes of a New P-N Ligand Ph2PCH2N(H)C5H3(Cl-5)N: Synthesis and Structural Studies. New J. Chem. 2001, 25, 416–422. DOI: https://doi.org/10.1039/b008502m.
- Durran, S. E.; Smith, M. B.; Dale, S. H.; Coles, S. J.; Hursthouse, M. B.; Light, M. E. New Pyridyl Modified Phosphines: Synthesis and Late Transition-Metal Coordination Studies. Inorg. Chim. Acta 2006, 359, 2980–2988. DOI: https://doi.org/10.1016/j.ica.2005.12.068.
- Jun-Feng, Z.; Xin, G.; Wen-Fu, F.; Xu, H.; Li, L. Interaction of Free Functional Group with Platinum(II) Center in Cyclometalated Complexes: A Structural and Photophysical Property Investigation. Inorg. Chim. Acta 2010, 363, 338–345. DOI: https://doi.org/10.1016/j.ica.2009.10.021.
- Li, N.-Y.; Ren, Z.-G.; Liu, D.; Yuan, R.-X.; Wei, L.-P.; Zhang, L.; Li, H.-X.; Lang, J.-P. Construction of [Ag2X2]-based complexes from reactions of Ag(I) salts with N-Diphenylphosphanylmethyl-4-Aminopyridine: Isolation, Structures, and Luminescent Properties. Dalton Trans. 2010, 39, 4213–4222. DOI: https://doi.org/10.1039/b925081f.
- Angurell, I.; Puig, E.; Rossell, O.; Seco, M.; Gómez-Sal, P.; Martín, A. Bifunctional N-P Ligands as Building Blocks for Construction of Multilayered Metallodendrimers. J. Organomet. Chem. 2012, 716, 120–128. DOI: https://doi.org/10.1016/j.jorganchem.2012.06.010.
- Zhang, J.-F.; Gan, X.; Xu, Q.-Q.; Chen, J.-H.; Yuan, M.; Fu, W.-F. Synthesis, Structures and Spectroscopic Properties of Platinum(II), Palladium(II) and Copper(I) Halide Complexes with Pyrimidine-Phosphine Ligand. Z Anorg. Allg. Chem. 2007, 633, 1718–1722. DOI: https://doi.org/10.1002/zaac.200700233.
- Kumar, S.; Mondal, D.; Balakrishna, M. S. Diverse Architectures and Luminescence Properties of Group 11 Complexes Containing Pyrimidine-Based Phosphine, N-((Diphenylphosphine)Methyl)Pyrimidin-2-Amine. ACS Omega. 2018, 3, 16601–16614. DOI: https://doi.org/10.1021/acsomega.8b02484.
- Zhang, J.-F.; Fu, W.-F.; Gan, X.; Chen, J.-H. Synthesis, Structures and Photophysical Properties of Luminescent Copper(I) and Platinum(II) Complexes with a Flexible Naphthyridine-Phosphine Ligand. Dalton Trans. 2008, 3093–3100. DOI: https://doi.org/10.1039/b717777a.
- Stephan, G. C.; Näther, C.; Sivasankar, C.; Tuczek, F. Mo– and W–N2 and –CO Complexes with Novel Mixed P/N Ligands: Structural Properties and Implications to Synthetic Nitrogen Fixation. Inorg. Chim. Acta 2008, 361, 1008–1019. DOI: https://doi.org/10.1016/j.ica.2007.06.046.
- Zhang, Y.-P.; Zhang, M.; Chen, X.-R.; Lu, C.; Young, D. J.; Ren, Z.-G.; Lang, J.-P. Cobalt(II) and Nickel(II) Complexes of a PNN Type Ligand as Photoenhanced Electrocatalysts for the Hydrogen Evolution Reaction. Inorg. Chem. 2020, 59, 1038–1045. DOI: https://doi.org/10.1021/acs.inorgchem.9b02497.
- Altan, O.; Serindağ, O.; Sayın, K.; Karakaş, D. Pd(II) Complexes of Novel Phosphine Ligands: Synthesis, Characterization, and Catalytic Activities on Heck Reaction. Phosphorus Sulfur Silicon Relat. Elem. 2016, 191, 993–999. DOI: https://doi.org/10.1080/10426507.2015.1119827.
- Dann, S. E.; Durran, S. E.; Elsegood, M. R. J.; Smith, M. B.; Staniland, P. M.; Talib, S.; Dale, S. H. Supramolecular Chemistry of Half-Sandwich Organometallic Building Blocks Based on RuCl2(p-Cymene)Ph2PCH2Y. J. Organomet. Chem. 2006, 691, 4829–4842. DOI: https://doi.org/10.1016/j.jorganchem.2006.07.036.
- Ramirez, B. L.; Sharma, P.; Eisenhart, R. J.; Gagliardi, L.; Lu, C. C. Bimetallic Nickel-Lutetium Complexes: Tuning the Properties and Catalytic Hydrogenation Activity of the Ni Site by Varying the Lu Coordination Environment. Chem. Sci. 2019, 10, 3375–3384. DOI: https://doi.org/10.1039/C8SC04712J.
- Du, J.; Huang, Z.; Zhang, Y.; Wang, S.; Zhou, S.; Fang, H.; Cui, P. A Scandium Metalloligand-Based Heterobimetallic Pd-Sc Complex: Electronic Tuning through a Very Short Pd→Sc Dative Bond. Chemistry 2019, 25, 10149–10155. DOI: https://doi.org/10.1002/chem.201901424.
- Brown, G. M.; Elsegood, M. R. J.; Lake, A. J.; Sanchez-Ballester, N. M.; Smith, M. B.; Varley, T. S.; Blann, K. Mononuclear and Heterodinuclear Metal Complexes of Nonsymmetric Ditertiary Phosphanes Derived from R2PCH2OH. Eur. J. Inorg. Chem. 2007, 1405–1414. DOI: https://doi.org/10.1002/ejic.200601199.
- Elsegood, M. R. J.; Lake, A. J.; Smith, M. B. A Novel Fluorene-Containing κ4-P2N2-Tetradentate Platinum(II) Complex. Dalton Trans. 2009, 30–32. DOI: https://doi.org/10.1039/B816351K.
- Kellner, K.; Hanke, W.; Tzschach, A. Zur Reaktion von Aminosäuren mit Formaldehyd und Sekundären Phosphinen. Z. Chem. 2010, 24, 193–194. DOI: https://doi.org/10.1002/zfch.19840240518.
- Peulecke, N.; Yakhvarov, D. G.; Heinicke, J. W. Chemistry of α-Phosphanyl α-Amino Acids. Eur. J. Inorg. Chem. 2019, 1507–1518. DOI: https://doi.org/10.1002/ejic.201801130.
- Lach, J.; Peulecke, N.; Kindermann, M. K.; Palm, G. J.; Köckerling, M.; Heinicke, J. W. α-Phosphanyl Amino Acids: Synthesis. Structure and Properties of Alkyl and Heterocyclic N-Substituted Siphenylphosphanylglycines. Tetrahedron 2015, 71, 4933–4945. DOI: https://doi.org/10.1016/j.tet.2015.05.101.
- Heinicke, J.; Peulecke, N.; Jones, P. G. Novel α-Functionally Substituted Amino Acids: Diphenylphosphinoglycines. Chem. Commun. 2005, 262–264. DOI: https://doi.org/10.1039/B412860E.
- Lach, J.; Guo, C.-Y.; Kindermann, M. K.; Jones, P. G.; Heinicke, J. α-Phosphanyl Amino Acids: Synthesis, Structure and Reactivity of N-Aryl-α-Phosphanylglycines. Eur. J. Org. Chem. 2010, 1176–1186. DOI: https://doi.org/10.1002/ejoc.200901251.
- Lach, J.; Peulecke, N.; Jones, P. G.; Dix, I.; Heinicke, J. W. α-Phosphanyl Amino Acids: Diphenylphosphanyl Glycines with a Chiral N-Substituent. Polyhedron 2016, 117, 795–802. DOI: https://doi.org/10.1016/j.poly.2016.07.011.
- Soficheva, O. S.; Kislitsyn, Y. A.; Nesterova, A. A.; Dobrynin, A. B.; Yakhvarov, D. G. Electrochemical Properties of N-Substituted α-Diphenylphosphinoglycines. Russ. J. Electrochem. 2020, 56, 431–436. DOI: https://doi.org/10.1134/S1023193520050109.
- Fomina, O. S.; Heinicke, J. W.; Sinyashin, O. G.; Yakhvarov, D. G. The Synthesis of Novel N-Heterocyclic α-Diphenylphosphinoglycines. Phosphorus Sulfur Silicon Relat. Elem. 2016, 191, 1478–1479. DOI: https://doi.org/10.1080/10426507.2016.1212046.
- Soficheva, O. S.; Nesterova, A. A.; Dobrynin, A. B.; Zueva, E. M.; Heinicke, J. W.; Sinyashin, O. G.; Yakhvarov, D. G. The Effect of N-Substituent on the Relative Thermodynamic Stability of Unionized and Zwitterionic Forms of α-Diphenylphosphino-α-Amino Acids. Mendeleev Commun. 2020, 30, 516–518. DOI: https://doi.org/10.1016/j.mencom.2020.07.038.
- Soficheva, O. S.; Bekmukhamedov, G. E.; Dobrynin, A. B.; Heinicke, J. W.; Sinyashin, O. G.; Yakhvarov, D. G. α-Diphenylphosphino-N-(Pyrazin-2-yl)Glycine as a Ligand in Ni-Catalyzed Ethylene Oligomerization. Mendeleev Commun. 2019, 29, 575–577. DOI: https://doi.org/10.1016/j.mencom.2019.09.033.
- Basvani, K. R.; Fomina, O. S.; Yakhvarov, D. G.; Heinicke, J. Synthesis and Properties of Zwitterionic Phosphonioglycolates. Polyhedron 2014, 67, 306–313. DOI: https://doi.org/10.1016/j.poly.2013.09.016.
- Peulecke, N.; Kindermann, M. K.; Köckerling, M.; Heinicke, J. Phosphonium Bis(Glycolates) and Phosphinoglycolates: Synthesis, Solvolysis, Oxidation to (Thio)Phosphinoylglycolates and Use as Ligands in Ni-Catalyzed Ethylene Oligomerization. Polyhedron 2012, 41, 61–69. DOI: https://doi.org/10.1016/j.poly.2012.04.019.
- Wu, P.; Givskov, M.; Nielsen, T. E. Reactivity and Synthetic Applications of Multicomponent Petasis Reactions. Chem. Rev. 2019, 119, 11245–11290. DOI: https://doi.org/10.1021/acs.chemrev.9b00214.
- Churches, Q. I.; Stewart, H. E.; Cohen, S. B.; Shröder, A.; Turner, P.; Hutton, C. A. Stereoselectivity of the Petasis Reaction with Various Chiral Amines and Styrenylboronic Acids. Pure Appl. Chem. 2008, 80, 687–694. DOI: https://doi.org/10.1351/pac200880040687.
- Heinicke, J.; Lach, J.; Peulecke, N.; Jones, P. G.; Dix, I. Phosphinoglycines and Phosphinoglycolates. Phosphorus Sulfur Silicon Relat. Elem. 2008, 183, 783–786. DOI: https://doi.org/10.1080/10426500701808101.
- Zhang, Q.; Ly, T.; Slawin, A. M. Z.; Woollins, J. D. Synthesis and Coordination of a New Bisaminomethylphosphine. Rev. Roum. Chim. 2002, 47, 1015–1020.
- Segawa, Y.; Yamashita, M.; Nozaki, K. Diphenylphosphino- or Dicyclohexylphosphino-Tethered Boryl Pincer Ligands: Syntheses of PBP Iridium(III) Complexes and Their Conversion to Iridium − Ethylene Complexes. Organometallics 2009, 28, 6234–6242. DOI: https://doi.org/10.1021/om9006455.
- Dixon, L. S. H.; Hill, A. F.; Sinha, A.; Ward, J. S. N-Heterocyclic Silyl Pincer Ligands. Organometallics 2014, 33, 653–658. DOI: https://doi.org/10.1021/om400792j.
- Segawa, Y.; Yamashita, M.; Nozaki, K. Syntheses of PBP Pincer Iridium Complexes: A Supporting Boryl Ligand. J. Am. Chem. Soc. 2009, 131, 9201–9203. DOI: https://doi.org/10.1021/ja9037092.
- Eizawa, A.; Arashiba, K.; Tanaka, H.; Kuriyama, S.; Matsuo, Y.; Nakajima, K.; Yoshizawa, K.; Nishibayashi, Y. Remarkable Catalytic Activity of Dinitrogen-Bridged Dimolybdenum Complexes Bearing NHC-Based PCP-Pincer Ligands toward Nitrogen Fixation. Nat. Commun. 2017, 8, id: 14874. DOI: https://doi.org/10.1038/ncomms14874.
- Tanoue, K.; Yamashita, M. Synthesis of Pincer Iridium Complexes Bearing a Boron Atom and iPr-Substituted Phosphorus Atoms: Application to Catalytic Transfer Dehydrogenation of Alkanes. Organometallics 2015, 34, 4011–4017. DOI: https://doi.org/10.1021/acs.organomet.5b00376.
- Eizawa, A.; Nishimura, S.; Arashiba, K.; Nakajima, K.; Nishibayashi, Y. Synthesis of Ruthenium Complexes Bearing PCP-Type Pincer Ligands and Their Application to Direct Synthesis of Imines from Amines and Benzyl Alcohol. Organometallics 2018, 37, 3086–3092. DOI: https://doi.org/10.1021/acs.organomet.8b00465.
- Takaoka, S.; Eizawa, A.; Kusumoto, S.; Nakajima, K.; Nishibayashi, Y.; Nozaki, K. Hydrogenation of Carbon Dioxide with Organic Base by PCIIP-Ir Catalysts. Organometallics 2018, 37, 3001–3009. DOI: https://doi.org/10.1021/acs.organomet.8b00377.
- Matoba, K.; Eizawa, A.; Nishimura, S.; Arashiba, K.; Nakajima, K.; Nishibayashi, Y. Practical Synthesis of a PCP-Type Pincer Ligand and Its Metal Complexes. Synthesis 2018, 50, 1015–1019. DOI: https://doi.org/10.1055/s-0036-1589153.
- Brugos, J.; Cabeza, J. A.; García-Álvarez, P.; Pérez-Carreño, E.; Polo, D. Synthesis and Some Coordination Chemistry of the PSnP Pincer-Type Stannylene Sn(NCH2PtBu2)2C6H4, Attempts to Prepare the PSiP Analogue, and the Effect of the E Atom on the Molecular Structures of E(NCH2PtBu2)2C6H4 (E = C, Si, Ge, Sn). Dalton Trans. 2018, 47, 4534–4544. DOI: https://doi.org/10.1039/C7DT04561A.
- Álvarez-Rodríguez, L.; Brugos, J.; Cabeza, J. A.; García-Álvarez, P.; Pérez-Carreño, E.; Polo, D. Synthesis and Initial Transition Metal Chemistry of the First PGeP Pincer-Type Germylene. Chem. Commun. 2017, 53, 893–896. DOI: https://doi.org/10.1039/C6CC09283G.
- Xiong, Z.; Li, X.; Zhang, S.; Shi, Y.; Sun, H. Synthesis and Reactivity of N-Heterocyclic PSiP Pincer Iron and Cobalt Complexes and Catalytic Application of Cobalt Hydride in Kumada Coupling Reactions. Organometallics 2016, 35, 357–363. DOI: https://doi.org/10.1021/acs.organomet.5b00937.
- Whited, M. T.; Deetz, A. M.; Boerma, J. W.; DeRosha, D. E.; Janzen, D. E. Formation of Chlorosilyl Pincer-Type Rhodium Complexes by Multiple Si–H Activations of Bis(Phosphine)/Dihydrosilyl Ligands. Organometallics 2014, 33, 5070–5073. DOI: https://doi.org/10.1021/om5006319.
- Wang, Y.; Zhang, H.; Xie, S.; Sun, H.; Li, X.; Fuhr, O.; Fenske, D. An Air-Stable N-Heterocyclic [PSiP] Pincer Iron Hydride and an Analogous Nitrogen Iron Hydride: Synthesis and Catalytic Dehydration of Primary Amides to Nitriles. Organometallics 2020, 39, 824–833. DOI: https://doi.org/10.1021/acs.organomet.9b00880.
- Ma, C. Coordination and Reactivity of Ligands with Unconventional ‘Donors’. Ph.D. Dissertation, The Australian National University, Canberra, Australia, 2018.
- Srungavruksham, N. K.; Liu, Y.-H.; Tsai, M.-K.; Chiu, C.-W. PSb+P Ligand: Platform for a Stibenium to Transition-Metal Interaction. Inorg. Chem. 2020, 59, 4468–4474. DOI: https://doi.org/10.1021/acs.inorgchem.9b03530.
- Sun, X.; Zhu, C. Synthesis, Characterization and Reactivity of a Neutral Antimony(III) Complex. Chin. Chem. Lett. 2021, 32, 717–720. DOI: https://doi.org/10.1016/j.cclet.2020.07.006.
- Sung, S.; Ang, A.; Hill, A. F.; Ma, C.; Kong, R. Y.; Ward, J. S.; Young, R. D. Bimetallic Complexes of Group 8, 9, and 11 Metals Bridged by RB(NCH2PPh2)2C6H4 (R = H, 4-C6H4X; X = H, Me, F) Ligands. Eur. J. Inorg. Chem. 2018, 2855–2864. DOI: https://doi.org/10.1002/ejic.201800448.
- Rudd, P. A.; Liu, S.; Gagliardi, L.; Young, V. G.; Lu, C. C. Metal–Alane Adducts with Zero-Valent Nickel, Cobalt, and Iron. J. Am. Chem. Soc. 2011, 133, 20724–20727. DOI: https://doi.org/10.1021/ja2099744.
- Clouston, L. J.; Siedschlag, R. B.; Rudd, P. A.; Planas, N.; Hu, S.; Miller, A. D.; Gagliardi, L.; Lu, C. C. Systematic Variation of Metal–Metal Bond Order in Metal–Chromium Complexes. J. Am. Chem. Soc. 2013, 135, 13142–13148. DOI: https://doi.org/10.1021/ja406506m.
- Rudd, P. A.; Liu, S.; Planas, N.; Bill, E.; Gagliardi, L.; Lu, C. C. Multiple Metal-metal Bonds in Iron-Chromium Complexes. Angew. Chem. Int. Ed. 2013, 52, 4449–4452. DOI: https://doi.org/10.1002/anie.201208686.
- Rudd, P. A.; Planas, N.; Bill, E.; Gagliardi, L.; Lu, C. C. Dinitrogen Activation at Iron and Cobalt Metallalumatranes. Eur. J. Inorg. Chem. 2013, 3898–3906. DOI: https://doi.org/10.1002/ejic.201300272.
- Ward, A. L.; Lukens, W. W.; Lu, C. C.; Arnold, J. Photochemical Route to Actinide-Transition Metal Bonds: Synthesis, Characterization and Reactivity of a Series of Thorium and Uranium Heterobimetallic Complexes. J. Am. Chem. Soc. 2014, 136, 3647–3654. DOI: https://doi.org/10.1021/ja413192m.
- Cammarota, R. C.; Lu, C. C. Tuning Nickel with Lewis Acidic Group 13 Metalloligands for Catalytic Olefin Hydrogenation. J. Am. Chem. Soc. 2015, 137, 12486–12489. DOI: https://doi.org/10.1021/jacs.5b08313.
- Eisenhart, R. J.; Rudd, P. A.; Planas, N.; Boyce, D. W.; Carlson, R. K.; Tolman, W. B.; Bill, E.; Gagliardi, L.; Lu, C. C. Pushing the Limits of Delta Bonding in Metal–Chromium Complexes with Redox Changes and Metal Swapping. Inorg. Chem. 2015, 54, 7579–7592. DOI: https://doi.org/10.1021/acs.inorgchem.5b01163.
- Ramirez, B. L.; Lu, C. C. Rare-Earth Supported Nickel Catalysts for Alkyne Semihydrogenation: Chemo- and Regioselectivity Impacted by the Lewis Acidity and Size of the Support. J. Am. Chem. Soc. 2020, 142, 5396–5407. DOI: https://doi.org/10.1021/jacs.0c00905.
- Prat, J. R.; Gaggioli, C. A.; Cammarota, R. C.; Bill, E.; Gagliardi, L.; Lu, C. C. Bioinspired Nickel Complexes Supported by an Iron Metalloligand. Inorg. Chem. 2020, 59, 14251–14262. DOI: https://doi.org/10.1021/acs.inorgchem.0c02041.
- Saito, T.; Hara, N.; Nakao, Y. Palladium Complexes Bearing Z-Type PAlP Pincer Ligands. Chem. Lett. 2017, 46, 1247–1249. DOI: https://doi.org/10.1246/cl.170421.
- Hara, N.; Saito, T.; Semba, K.; Kuriakose, N.; Zheng, H.; Sakaki, S.; Nakao, Y. Rhodium Complexes Bearing PAlP Pincer Ligands. J. Am. Chem. Soc. 2018, 140, 7070–7073. DOI: https://doi.org/10.1021/jacs.8b04199.
- Hara, N.; Yamamoto, K.; Tanaka, Y.; Saito, T.; Sakaki, S.; Nakao, Y. Synthesis, Electronic Properties, and Lewis Acidity of Rhodium Complexes Bearing X-Type PBP, PAlP, and PGaP Pincer Ligands. Bull. Chem. Soc. Jpn. 2021, 94, 1859–1868. DOI: https://doi.org/10.1246/bcsj.20210068.
- Ben-Aroya, B. B.-N.; Portnoy, M. Solid-Phase Synthesis of an α-Aminophosphine Library. J. Comb. Chem. 2001, 3, 524–527. DOI: https://doi.org/10.1021/cc0100363.
- Slany, M.; Höhn, A. Cis-verbrückte Metallkomplexe. Ger. Patent 196 51 685, Aug 20, 1998.
- Buenaflor, J.; Sommerville, P.; Qian, H.; Luscombe, C. Investigation of Bimetallic Nickel Catalysts in Catalyst‐Transfer Polymerization of π‐Conjugated Polymers. Macromol. Chem. Phys. 2020, 221, id: 1900363. DOI: https://doi.org/10.1002/macp.201900363.
- Durran, S. E.; Elsegood, M. R. J.; Hawkins, N.; Smith, M. B.; Talib, S. New Functionalised Ditertiary Phosphines via Phosphorus Based Mannich Condensation Reactions. Tetrahedron Lett. 2003, 44, 5255–5257. DOI: https://doi.org/10.1016/S0040-4039(03)01273-5.
- Reetz, M. T.; Waldvogel, S. R.; Goddard, R. Substituent Effects in the Rhodium-Catalyzed Hydroformylation of Olefins Using Bis(Diarylphosphino)Methylamino Ligands. Tetrahedron Lett. 1997, 38, 5967–5970. DOI: https://doi.org/10.1016/S0040-4039(97)01345-2.
- Seo, J.; Pekarek, R. T.; Rose, M. J. Photoelectrochemical Operation of a Surface-Bound, Nickel-Phosphine H2 Evolution Catalyst on p-Si(111): A Molecular Semiconductor|Catalyst Construct. Chem. Commun. 2015, 51, 13264–13267. DOI: https://doi.org/10.1039/C5CC02802G.
- Garrett, B. R.; Awad, A.; He, M.; Click, K. A.; Durr, C. B.; Gallucci, J. C.; Hadad, C. M.; Wu, Y. Dimeric FeFe-Hydrogenase Mimics Bearing Carboxylic Acids: Synthesis and Electrochemical Investigation. Polyhedron 2016, 103, 21–27. DOI: https://doi.org/10.1016/j.poly.2015.08.019.
- Keleş, M.; Yılmaz, M. K. Palladium(II) Complexes with Aminomethylphosphine Ligands as Catalysts for the Heck Reaction. Heteroatom Chem. 2012, 23, 466–471. DOI: https://doi.org/10.1002/hc.21038.
- Kim, H. J.; Seo, J.; Rose, M. J. H2 Photogeneration Using a Phosphonate-Anchored Ni-PNP Catalyst on a Band-Edge-Modified p-Si(111)|AZO Construct. ACS Appl. Mater. Interfaces 2016, 8, 1061–1066. DOI: https://doi.org/10.1021/acsami.5b09902.
- Dolaz, M.; Uruş, S.; Ceyhan, G. Synthesis, Characterization and Catalytic Properties of Benzylphosphonate-aminethylphosphine-Pd(II), Cu(II), Ru(II) and V(IV) Complexes. J. Inorg. Organomet. Polym. 2019, 29, 1575–1586. DOI: https://doi.org/10.1007/s10904-019-01121-3.
- Keles, M.; Aydin, Z.; Serindag, O. Synthesis of Palladium Complexes with Bis(Diphenylphosphinomethyl)Amino Ligands: A Catalyst for the Heck Reaction of Aryl Halide with Methyl Acrylate. J. Organomet. Chem. 2007, 692, 1951–1955. DOI: https://doi.org/10.1016/j.jorganchem.2007.01.003.
- Keleş, M.; Altan, O.; Serindaǧ, O. Synthesis and Characterization of Bis(Diphenylphosphinomethyl)Amino Ligands and Their Ni(II), Pd(II) Complexes: Application to Hydrogenation of Styrene. Heteroatom Chem. 2008, 19, 113–118. DOI: https://doi.org/10.1002/hc.20384.
- De'Ath, P.; Elsegood, M. R. J.; Halliwell, C. A. G.; Smith, M. B. Mild Intramolecular P–C(sp3) Bond Cleavage in Bridging Diphosphine Complexes of RuII RhIII and IrIII. J. Organomet. Chem. 2021, 937, id: 121704. DOI: https://doi.org/10.1016/j.jorganchem.2021.121704.
- Smith, M. B.; Dale, S. H.; Coles, S. J.; Gelbrich, T.; Hursthouse, M. B.; Light, M. E.; Horton, P. N. Hydrogen Bonded Supramolecular Assemblies Based on Neutral Square-Planar Palladium(II) Complexes. CrystEngComm 2007, 9, 165–175. DOI: https://doi.org/10.1039/b616337h.
- Elsegood, M. R. J.; Smith, M. B.; Staniland, P. M. Neutral Molecular Pd6 Hexagons Using κ3-P2O-Terdentate Ligands. Inorg. Chem. 2006, 45, 6761–6770. DOI: https://doi.org/10.1021/ic060629o.
- Smith, M. B.; Dale, S. H.; Coles, S. J.; Gelbrich, T.; Hursthouse, M. B.; Light, M. E. Isomeric Dinuclear Gold(I) Complexes with Highly Functionalised Ditertiary Phosphines: Self-Assembly of Dimers, Rings and 1-D Polymeric Chains. CrystEngComm 2006, 8, 140–149. DOI: https://doi.org/10.1039/b516023e.
- Serindaǧ, O. Synthesis of a Crown Ether Functionalized Phosphine and Its Nickel(II), Palladium(II) and Platinum(II) Complexes. Synth. React. Inorg. Met. Org. Chem. 1995, 25, 327–335. DOI: https://doi.org/10.1080/15533179508218223.
- Ezzaher, S.; Capon, J.-F.; Gloaguen, F.; Pétillon, F. Y.; Schollhammer, P.; Talarmin, J.; Kervarec, N. Influence of a Pendant Amine in the Second Coordination Sphere on Proton Transfer at a Dissymmetrically Disubstituted Diiron System Related to the [2Fe]H Subsite of [FeFe]H2ase. Inorg. Chem. 2009, 48, 2–4. DOI: https://doi.org/10.1021/ic801369u.
- Weiss, C. J.; Groves, A. N.; Mock, M. T.; Dougherty, W. G.; Kassel, W. S.; Helm, M. L.; DuBois, D. L.; Bullock, R. M. Synthesis and Reactivity of Molybdenum and Tungsten Bis(Dinitrogen) Complexes Supported by Diphosphine Chelates Containing Pendant Amines. Dalton Trans. 2012, 41, 4517–4529. DOI: https://doi.org/10.1039/c2dt12224c.
- Redin, K.; Wilson, A. D.; Newell, R.; DuBois, M. R.; DuBois, D. L. Studies of Structural Effects on the Half-Wave Potentials of Mononuclear and Dinuclear Nickel(II) Diphosphine/Dithiolate Complexes. Inorg. Chem. 2007, 46, 1268–1276. DOI: https://doi.org/10.1021/ic061740x.
- Uruş, S.; Serindağ, O.; Diğrak, M. Synthesis, Characterization, and Antimicrobial Activities of Cu(I), Ag(I), Au(I), and Co(II) Complexes with [CH3N(CH2PPh2)2]. Heteroatom Chem. 2005, 16, 484–491. DOI: https://doi.org/10.1002/hc.20145.
- Willocq, C.; Vidick, D.; Tinant, B.; Delcorte, A.; Bertrand, P.; Devillers, M.; Hermans, S. Anchoring of Ru–Pt and Ru–Au Clusters onto a Phosphane‐Functionalized Carbon Support. Eur. J. Inorg. Chem. 2011, 4721–4729. DOI: https://doi.org/10.1002/ejic.201100384.
- Klemps, C.; Payet, E.; Magna, L.; Saussine, L.; Le Goff, X. F.; Le Floch, P. PCNCP Ligands in the Chromium-Catalyzed Oligomerization of Ethylene: Tri- versus Tetramerization. Chemistry 2009, 15, 8259–8268. DOI: https://doi.org/10.1002/chem.200900986.
- Wu, W.; Li, C.-J. A Highly Regio- and Stereoselective Transition Metal-Catalyzed Hydrosilylation of Terminal Alkynes under Ambient Conditions of Air, Water, and Room Temperature. Chem. Commun. 2003, 1668–1669. DOI: https://doi.org/10.1039/b302259e.
- Yerlikay, G.; Tapanyiğit, E. B.; Güzel, B.; Şahin, O.; Kardaş, G. Synthesis of Phosphine-Containing Novel Pd(II) and Ni(II) Complexes: Electrochemical, Photophysical and Quantum Chemical Studies. J. Mol. Struct. 2019, 1198, id: 126889. DOI: https://doi.org/10.1016/j.molstruc.2019.126889.
- Keleş, M.; Keleş, T.; Serindağ, O. Palladium Complexes with Bis(Diphenylphosphinomethyl)Amino Ligands and Their Application as Catalysts for the Heck Reaction. Transition Met. Chem. 2008, 33, 717–720. DOI: https://doi.org/10.1007/s11243-008-9101-z.
- Zhang, J.; Vittal, J. J.; Henderson, W.; Wheaton, J. R.; Hall, I. H.; Hor, T. S. A.; Yan, Y. K. Tricarbonylrhenium(I) Complexes of Phosphine-Derivatized Amines, Amino Acids and a Model Peptide: Structures, Solution Behavior and Cytotoxicity. J. Organomet. Chem. 2002, 650, 123–132. DOI: https://doi.org/10.1016/S0022-328X(02)01200-7.
- Zhang, Q.; Hua, G.; Bhattacharyya, P.; Slawin, A. M. Z.; Woollins, J. D. Syntheses and Coordination Chemistry of Aminomethylphosphine Derivatives of Adenine. Eur. J. Inorg. Chem. 2003, 2426–2437. DOI: https://doi.org/10.1002/ejic.200300037.
- Román-Martı́nez, M. C.; Dı́az-Auñón, J. A.; de Lecea, C. S.-M.; Alper, H.; Rhodium-Diphosphine Complex Bound to Activated Carbon: An Effective Catalyst for the Hydroformylation of 1-Octene. J. Mol. Catal. A: Chem. 2004, 213, 177–182. DOI: https://doi.org/10.1016/j.molcata.2003.12.015.
- Servin, P.; Laurent, R.; Romerosa, A.; Peruzzini, M.; Majoral, J.-P.; Caminade, A.-M. Synthesis of Dendrimers Terminated by Bis(Diphenylphosphinomethyl)Amino Ligands and Use of Their Palladium Complexes for Catalyzing C − C Cross-Coupling Reactions. Organometallics 2008, 27, 2066–2073. DOI: https://doi.org/10.1021/om800008p.
- Durran, S. E.; Elsegood, M. R. J.; Smith, M. B. New Complexes of Functionalised Ligands Bearing P/N/Se or P2Se Donor Sets. New J. Chem. 2002, 26, 1402–1408. DOI: https://doi.org/10.1039/b204005k.
- Keleş, M.; Keleş, T.; Serindağ, O.; Yaşar, S.; Özdemir, İ. Hydrogenation of Acetophenone and Its Derivatives with 2-Propanol Using Aminomethylphosphine-Ruthenium Catalysis. Phosphorus Sulfur Silicon Relat. Elem. 2009, 185, 165–170. DOI: https://doi.org/10.1080/10426500902754278.
- Posset, T.; Guenther, J.; Pope, J.; Oeser, T.; Blümel, J. Immobilized Sonogashira Catalyst Systems: New Insights by Multinuclear HRMAS NMR Studies. Chem. Commun. 2011, 47, 2059–2061. DOI: https://doi.org/10.1039/C0CC04194G.
- Penney, M. K.; Giang, R.; Klausmeyer, K. K. Single, Double, and Triple Silver Centers Bound by a Tetradentate N,P Ligand. Polyhedron 2015, 85, 275–283. DOI: https://doi.org/10.1016/j.poly.2014.08.017.
- Penney, M. K.; Giang, R.; Burroughs, M. A.; Klausmeyer, K. K. Structure and Luminescence of Discrete and Polymeric Ag(I) Complexes Formed by the Multidentate Pyridylphosphine (PPh2CH2)2N(3-CH2C5H4N). Polyhedron 2015, 87, 43–54. DOI: https://doi.org/10.1016/j.poly.2014.11.002.
- Angurell, I.; Rossell, O.; Seco, M. Synthesis of Carbosilane Dendrimers Containing up to Four Metal Layers. Chemistry 2009, 15, 2932–2940. DOI: https://doi.org/10.1002/chem.200802479.
- Siebert, M.; Seibicke, M.; Siegle, A. F.; Kräh, S.; Trapp, O. Selective Ruthenium-Catalyzed Transformation of Carbon Dioxide: An Alternative Approach toward Formaldehyde. J. Am. Chem. Soc. 2019, 141, 334–341. DOI: https://doi.org/10.1021/jacs.8b10233.
- Huang, T.-H.; Luo, C.; Zheng, D.; Tan, J.-Y.; Liu, Y.; Tang, J. Synthesis, Structures, DFT Studies and Properties of Novel Tertiary Diphosphines Based on α- and β-Naphthylamine. J. Mol. Struct. 2022, 1247, id: 131375. DOI: https://doi.org/10.1016/j.molstruc.2021.131375.
- De’Ath, P.; Elsegood, M. R. J.; Sanchez-Ballester, N. M.; Smith, M. B. Low-Dimensional Architectures in Isomeric cis-PtCl2{Ph2PCH2N(Ar)CH2PPh2} Complexes Using Regioselective-N(Aryl)-Group Manipulation. Molecules 2021, 26, 6809. DOI: https://doi.org/10.3390/molecules26226809.
- Viertl, W.; Pann, J.; Pehn, R.; Roithmeyer, H.; Bendig, M.; Rodríguez-Villalón, A.; Bereiter, R.; Heiderscheid, M.; Müller, T.; Zhao, X.; et al. Performance of Enhanced DuBois Type Water Reduction Catalysts (WRC) in Artificial Photosynthesis - Effects of Various Proton Relays During Catalysis. Faraday Discuss. 2019, 215, 141–161. DOI: https://doi.org/10.1039/C8FD00162F.
- Pehn, R.; Pann, J.; Ehrmann, K.; Viertl, W.; Roithmeyer, H.; Bendig, M.; Strabler, C.; Kopacka, H.; Müller, T.; Hofer, T.; Brüggeller, P. Versatile Production of Novel PNP Based Metal Complexes Applicable as Water Reduction Catalysts Showing CH/M as Well as CH/π Interactions. Eur. J. Inorg. Chem. 2020, 4358–4372. DOI: https://doi.org/10.1002/ejic.202000778.
- Walsh, A. P.; Laureanti, J. A.; Katipamula, S.; Chambers, G. M.; Priyadarshani, N.; Lense, S.; Bays, J. T.; Linehan, J. C.; Shaw, W. J. Evaluating the Impacts of Amino Acids in the Second and Outer Coordination Spheres of Rh-Bis(Diphosphine) Complexes for CO2 Hydrogenation. Faraday Discuss. 2019, 215, 123–140. DOI: https://doi.org/10.1039/C8FD00164B.
- Curtis, C. J.; Miedaner, A.; Ciancanelli, R.; Ellis, W. W.; Noll, B. C.; DuBois, M. R.; DuBois, D. L. [Ni(Et2PCH2NMeCH2PEt2)2]2+ as a Functional Model for Hydrogenases. Inorg. Chem. 2003, 42, 216–227. DOI: https://doi.org/10.1021/ic020610v.
- DuBois, D. L.; DuBois, M. R. Nickel Complexes of Bis(Diethylphosphinomethyl)Methylamine. In Inorganic Syntheses; Rauchfuss, T. B., Ed.; John Wiley & Sons: New Jersey, 2010; Vol. 35, pp. 132–137. DOI: https://doi.org/10.1002/9780470651568.ch7.
- Darmon, J. M.; Raugei, S.; Liu, T.; Hulley, E. B.; Weiss, C. J.; Bullock, R. M.; Helm, M. L. Iron Complexes for the Electrocatalytic Oxidation of Hydrogen: Tuning Primary and Secondary Coordination Spheres. ACS Catal. 2014, 4, 1246–1260. DOI: https://doi.org/10.1021/cs500290w.
- Labios, L. A.; Weiss, C. J.; Egbert, J. D.; Lense, S.; Bullock, R. M.; Dougherty, W. G.; Kassel, W. S.; Mock, M. T. Synthesis and Protonation Studies of Molybdenum(0) Bis(Dinitrogen) Complexes Supported by Diphosphine Ligands Containing Pendant Amines. Z Anorg. Allg. Chem. 2015, 641, 105–117. DOI: https://doi.org/10.1002/zaac.201400119.
- Darmon, J. M.; Kumar, N.; Hulley, E. B.; Weiss, C. J.; Raugei, S.; Bullock, R. M.; Helm, M. L. Increasing the Rate of Hydrogen Oxidation without Increasing the Overpotential: A Bio-Inspired Iron Molecular Electrocatalyst with an Outer Coordination Sphere Proton Relay. Chem. Sci. 2015, 6, 2737–2745. DOI: https://doi.org/10.1039/C5SC00398A.
- Kumar, N.; Darmon, J. M.; Weiss, C. J.; Helm, M. L.; Raugei, S.; Bullock, R. M. Outer Coordination Sphere Proton Relay Base and Proximity Effects on Hydrogen Oxidation with Iron Electrocatalysts. Organometallics 2019, 38, 1391–1396. DOI: https://doi.org/10.1021/acs.organomet.8b00805.
- Kruckenberg, A.; Wadepohl, H.; Gade, L. H. Bis(Diisopropylphosphinomethyl)Amine Nickel(II) and Nickel(0) Complexes: Coordination Chemistry, Reactivity, and Catalytic Decarbonylative C–H Arylation of Benzoxazole. Organometallics 2013, 32, 5153–5170. DOI: https://doi.org/10.1021/om400711d.
- Heuzé, K.; Méry, D.; Gauss, D.; Blais, J. C.; Astruc, D. Copper-free Monomeric and Dendritic Palladium Catalysts for the Sonogashira Reaction: Substituent Effects, Synthetic Applications, and the Recovery and Re-use of the Catalysts. Chemistry 2004, 10, 3936–3944. DOI: https://doi.org/10.1002/chem.200400150.
- Méry, D.; Heuzé, K.; Astruc, D. A. Very Efficient, Copper-Free Palladium Catalyst for the Sonogashira Reaction with Aryl Halides. Chem. Commun. 2003, 1934–1935. DOI: https://doi.org/10.1039/B305391C.
- Serindag, O.; Kemmitt, R. D. W.; Fawcett, J.; Russell, D. R. Preparation and Reaction of Platinum(II) Complexes of N,N-Bis(Dicyclohexylphosphinomethyl)Aminomethane. Crystal Structures of (Cy2PCH2)2NMe (Cy = Cyclohexyl) and [PtX2{(Cy2PCH2)2NMe}], (X = Cl and I). Transit. Met. Chem. 1999, 24, 486–491. DOI: https://doi.org/10.1023/A:1006916608831.
- Gatard, S.; Nlate, S.; Cloutet, E.; Bravic, G.; Blais, J.-C.; Astruc, D. Dendritic Stars by Ring-Opening-metathesis Polymerization from Ruthenium-Carbene Initiators. Angew. Chem. Int. Ed. 2003, 42, 452–456. DOI: https://doi.org/10.1002/anie.200390137.
- Phanopoulos, A.; White, A. J. P.; Long, N. J.; Miller, P. W. Insight into the Stereoelectronic Parameters of N‐Triphos Ligands via Coordination to Tungsten(0). Dalton Trans. 2016, 45, 5536–5548. DOI: https://doi.org/10.1039/C6DT00170J.
- Heuzé, K.; Fougeret, A.; Lemo, J.; Rosario-Amorin, D. C–C or C–N Reactions Catalyzed by Diadamanthylphosphine Palladium-Based Catalyst Supported on DAB-Dendrimers. In Solid-Phase Organic Syntheses; Scott, P. J. H., Ed.; John Wiley&Sons: New Jersey, 2012; Vol. 2, pp. 97–104. DOI: https://doi.org/10.1002/9781118336953.ch11.
- Fillol, J. L.; Kruckenberg, A.; Scherl, P.; Wadepohl, H.; Gade, L. H. Stitching Phospholanes Together Piece by Piece: New Modular Di- and Tridentate Stereodirecting Ligands. Chem. Eur. J. 2011, 17, 14047–14062. DOI: https://doi.org/10.1002/chem.201101864.
- Keglevich, G.; Szekrényi, A.; Szöllősy, Á.; Drahos, L. Synthesis of Bis(Phosphonatomethyl)-, Bis(Phosphinatomethyl)-, and Bis(Phosphinoxidomethyl)Amines, as Well as Related Ring Bis(Phosphine) Platinum Complexes. Synth. Commun. 2011, 41, 2265–2272. DOI: https://doi.org/10.1080/00397911.2010.501478.
- Bálint, E.; Fazekas, E.; Pintér, G.; Szollosy, A.; Holczbauer, T.; Czugler, M.; Drahos, L.; Körtvélyesi, T.; Keglevich, G. Synthesis and Utilization of the Bis(>P(O)CH2)Amine Derivatives Obtained by the Double Kabachnik–Fields Reaction with Cyclohexylamine; Quantum Chemical and X-Ray Study of the Related Bidentate Chelate Platinum Complexes. 2012, 16, 547–554. DOI: https://doi.org/10.2174/138527212799499822.
- Bálint, E.; Fazekas, E.; Pongrácz, P.; Kollár, L.; Drahos, L.; Holczbauer, T.; Czugler, M.; Keglevich, G. N-Benzyl and N-Aryl Bis(phospha-Mannich Adducts): Synthesis and Catalytic Activity of the Related Bidentate Chelate Platinum Complexes in Hydroformylation. J. Organomet. Chem. 2012, 717, 75–82. DOI: https://doi.org/10.1016/j.jorganchem.2012.07.031.
- Bálint, E.; Tripolszky, A.; Jablonkai, E.; Karaghiosoff, K.; Czugler, M.; Mucsi, Z.; Kollár, L.; Pongrácz, P.; Keglevich, G. Synthesis and Use of α-Aminophosphine Oxides and N,N-Bis(Phosphinoylmethyl)Amines – a Study on the Related Ring Platinum Complexes. J. Organomet. Chem. 2016, 801, 111–121. DOI: https://doi.org/10.1016/j.jorganchem.2015.10.029.
- Bálint, E.; Tajti, Á.; Kalocsai, D.; Mátravölgyi, B.; Karaghiosoff, K.; Czugler, M.; Keglevich, G. Synthesis and Utilization of Optically Active α-Aminophosphonate Derivatives by Kabachnik-Fields Reaction. Tetrahedron 2017, 73, 5659–5667. DOI: https://doi.org/10.1016/j.tet.2017.07.060.
- Tripolszky, A.; Bálint, E.; Keglevich, G. Microwave-Assisted Synthesis of α-Aminophosphine Oxides. Phosphorus Sulfur Silicon Relat. Elem. 2019, 194, 345–348. DOI: https://doi.org/10.1080/10426507.2018.1541898.
- Sowa, S.; Stankevič, M.; Flis, A.; Pietrusiewicz, K. M. Reduction of Tertiary Phosphine Oxides by BH3 Assisted by Neighboring Activating Groups. Synthesis 2018, 50, 2106–2118. DOI: https://doi.org/10.1055/s-0036-1591546.
- Bays, J. T.; Priyadarshani, N.; Jeletic, M. S.; Hulley, E. B.; Miller, D. L.; Linehan, J. C.; Shaw, W. J. The Influence of the Second and Outer Coordination Spheres on Rh(Diphosphine)2 CO2 Hydrogenation Catalysts. ACS Catal. 2014, 4, 3663–3670. DOI: https://doi.org/10.1021/cs5009199.
- Wise, D. E. Rational Phosphine Design for Cytotoxic Ru Complexes, Luminescent Compounds and Allylation Catalysts. Ph.D. Dissertation, the University of Bristol, Bristol, UK, 2021.
- Laureanti, J. A.; Buchko, G. W.; Katipamula, S.; Su, Q.; Linehan, J. C.; Zadvornyy, O. A.; Peters, J. W.; O’Hagan, M. Protein Scaffold Activates Catalytic CO2 Hydrogenation by a Rhodium Bis(Diphosphine) Complex. ACS Catal. 2019, 9, 620–625. DOI: https://doi.org/10.1021/acscatal.8b02615.
- Märkl, G.; Jin, G. Y. Optisch Aktive N.N-Bis [Phosphinomethylen]-Aminosäureester und Deren Molybdäncarbonyl-Komplexe. Tetrahedron Lett. 1981, 22, 223–226. DOI: https://doi.org/10.1016/0040-4039(81)80060-3.
- Roy, S.; Mazinani, S. K. S.; Groy, T. L.; Gan, L.; Tarakeshwar, P.; Mujica, V.; Jones, A. K. Catalytic Hydrogen Evolution by Fe(II) Carbonyls Featuring a Dithiolate and a Chelating Phosphine. Inorg. Chem. 2014, 53, 8919–8929. DOI: https://doi.org/10.1021/ic5012988.
- Elsegood, M. R. J.; Lake, A. J.; Elliott, C. L.; Smith, M. B.; Weaver, G. W. Late Transition Metal Complexes of a Coumarin-Functionalized Ditertiary Phosphine. Phosphorus Sulfur Silicon Relat. Elem. 2008, 183, 435–439. DOI: https://doi.org/10.1080/10426500701735536.
- Elsegood, M. R. J.; Noble, T. A.; Talib, S.; Smith, M. B. A Simple Procedure to Ditertiary Phosphinocarboxylic Acids and Their Bisphosphine Oxides. Phosphorus Sulfur Silicon Relat. Elem. 2013, 188, 121–127. DOI: https://doi.org/10.1080/10426507.2012.743133.
- Serindag, O.; Kemmitt, R. D. W.; Fawcett, J.; Russell, D. R. Synthesis of Sulphonated Aminomethylphosphines and Some Nickel(II), Palladium(II), Platinum(II) and Rhodium(I) Complexes. Crystal Structure of [Et3NH][(Ph2PCH2)2N(CH2)2SO3]. Transition Met. Chem. 1995, 20, 548–551. DOI: https://doi.org/10.1007/BF00136417.
- Ma, X. B.; Fu, X. K. Synthesis of a New Type of Amphilic and Water-Soluble Tertiary Phosphine Ligands Substituted by an Ethoxylated Phosphonic Acid Chain and Their Palladium Complexes. J. Mol. Catal. A: Chem. 2003, 195, 47–53. DOI: https://doi.org/10.1016/S1381-1169(02)00549-6.
- Reetz, M. T.; Waldvogel, S. R. β-Cyclodextrin-Modified Diphosphanes as Ligands for Supramolecular Rhodium Catalysts. Angew. Chem. Int. Ed. 1997, 36, 865–867. DOI: https://doi.org/10.1002/anie.199708651.
- Reetz, M. T.; Waldvogel, S. Olefin Hydroformylation Process in a Two-Phase System. World Patent 98/05618, Feb 12, 1998.
- Vigo, S.; Andrés, R.; Gómez-Sal, P.; de la Mata, J.; de Jesús, E. Synthesis of Palladium(II) Complexes of Bidentate Phosphano Ligands with Carbosilane Substituents. J. Organomet. Chem. 2012, 717, 88–98. DOI: https://doi.org/10.1016/j.jorganchem.2012.07.032.
- Märk, G.; Jin, G. Y. N.N.N-Tris[Phosphinomethylen]Amine N.N.N′-Tris[Phosphinomethylen]Hydrazine N.N.N′.N′-Tetra[Phosphinomethylen]Hydrazine. Tetrahedron Lett. 1981, 22, 1105–1108. DOI: https://doi.org/10.1016/S0040-4039(01)90248-5.
- Maraval, V.; Laurent, R.; Caminade, A.-M.; Majoral, J.-P. Phosphorus-Containing Dendrimers and Their Transition Metal Complexes as Efficient Recoverable Multicenter Homogeneous Catalysts in Organic Synthesis. Organometallics 2000, 19, 4025–4029. DOI: https://doi.org/10.1021/om0005607.
- Maraval, V.; Laurent, R.; Donnadieu, B.; Mauzac, M.; Caminade, A.-M.; Majoral, J.-P. Rapid Synthesis of Phosphorus-Containing Dendrimers with Controlled Molecular Architectures: First Example of Surface-Block, Layer-Block, and Segment-Block Dendrimers Issued from the Same Dendron. J. Am. Chem. Soc. 2000, 122, 2499–2511. DOI: https://doi.org/10.1021/ja992099j.
- Bardaji, M.; Kustos, M.; Caminade, A.-M.; Majoral, J.-P.; Chaudret, B. Phosphorus-Containing Dendrimers as Multidentate Ligands: Palladium, Platinum, and Rhodium Complexes. Organometallics 1997, 16, 403–410. DOI: https://doi.org/10.1021/om9606101.
- Bardají, M.; Caminade, A.-M.; Majoral, J.-P.; Chaudret, B. Ruthenium Hydride and Dihydrogen Complexes with Dendrimeric Multidentate Ligands. Organometallics 1997, 16, 3489–3497. DOI: https://doi.org/10.1021/om970092+.
- Caminade, A.-M.; Laurent, R.; Ouali, A.; Majoral, J.-P. Poly(Phosphorhydrazone) Metallodendrimers. A Review. Inorg. Chim. Acta 2014, 409, 68–88. DOI: https://doi.org/10.1016/j.ica.2013.06.022.
- Caminade, A.-M.; Ouali, A.; Laurent, R.; Majoral, J.-P. Phosphorus Dendrimers as Supports of Transition Metal Catalysts. Inorg. Chim. Acta 2015, 431, 3–20. DOI: https://doi.org/10.1016/j.ica.2014.10.035.
- Caminade, A.-M.; Majoral, J.-P. Bifunctional Phosphorus Dendrimers and Their Properties. Molecules 2016, 21, id: 538. DOI: https://doi.org/10.3390/molecules21040538.
- Yi, T.; Mo, M.; Fu, H.-Y.; Li, R.-X.; Chen, H.; Li, X.-J. Highly Efficient Pd/Tetraphosphine Catalytic System for Copper-Free Sonogashira Reactions of Aryl Bromides with Terminal Alkynes. Catal. Lett. 2012, 142, 594–600. DOI: https://doi.org/10.1007/s10562-012-0796-2.
- Matienzo, L. J.; Grim, S. O.; Uriarte, R.; Meek, D. W. N,N,N′,N′‐Tetrakis(Diphenylphosphinomethyl)‐Ethylenediamine. Inorg. Synth. 1976, 16, 198–199. DOI: https://doi.org/10.1002/9780470132470.ch53.
- Fernández, E. J.; Laguna, A.; Monge, M.; Montiel, M.; Olmos, M. E.; Pérez, J.; Sánchez-Forcada, E. Dendritic (Phosphine)Gold(I) Thiolate Complexes: Assessment of the Molecular Size through PGSE NMR Studies. Dalton Trans. 2009, 474–480. DOI: https://doi.org/10.1039/B812500G.
- Zhang, Y.; Yi, T.; Wang, K.; Fu, H.; Chen, H.; Li, R. A New Tetraphosphine and Its Application in Pd-Catalyzed Suzuki Cross-Coupling Reaction Chin. J. Org. Chem. 2012, 32, 790–793. DOI: https://doi.org/10.6023/cjoc1108181.
- Pann, J.; Ehrmann, K.; Pehn, R.; Roithmeyer, H.; Viertl, W.; Kopacka, H.; Brüggeller, P.; Oberhauser, W. Cu(I) Coordination by N,N,N’,N’-Tetra(di-Ortho-Anisylphosphanylmethyl) Ethylene and Propylene Diamine: First Example of a Sandwiched CuCl-Tetramer. Inorg. Chim. Acta 2021, 516, id: 120162. DOI: https://doi.org/10.1016/j.ica.2020.120162.
- Ni, Q.-L.; Uao, Y.-F.; Ge, C.-Y.; Gui, L.-C.; Tang, L.-H.; Wang, X.-J. Synthesis and Crystal Structure of N,N,N',N'-Tetra[(Diphenylphosphine)Ethyl]-1,4-Phenylenediamine. Chem. Res. Appl. 2008, 20, 617–620.
- Uruş, S.; İncesu, M.; Köşker, S.; Kurt, A. H.; Ceyhan, G. Synthesis, Characterization, Photoluminescence and Electrochemical Properties of Pt(II) and Ag(I) Complexes of Tetradentate Aminomethylphosphine Ligands and Antiproliferative Activities on HT‐29 Human Colon Cancer. Appl. Organometal. Chem. 2017, 31, id: e3550. DOI: https://doi.org/10.1002/aoc.3550.
- Wang, K.; Wang, W.; Luo, H.; Zheng, X.; Fu, H.; Chen, H.; Li, R. An Easily Prepared Tetraphosphine and Its Use in the Palladium-Catalyzed Suzuki–Miyaura Coupling of Aryl Chlorides. Catal. Lett. 2013, 143, 1214–1219. DOI: https://doi.org/10.1007/s10562-013-1028-0.
- Uruş, S.; Keleş, M.; Köşker, S. Synthesis and Characterization of Pd(II) and Ru(II) Complexes of Tetradentate N,N,N,N-(Diphosphinomethyl)Amine Ligands: Catalytic Properties in Transfer Hydrogenation and Heck Coupling Reactions. Heterocycles 2020, 100, 1019–1034. DOI: https://doi.org/10.3987/COM-20-14260.
- Zhou, R.; Wang, W.; Jiang, Z.-J.; Fu, H.-Y.; Zheng, X.-L.; Zhang, C.-C.; Chen, H.; Li, R.-X. Pd/Tetraphosphine Catalytic System for Cu-Free Sonogashira Reaction “on Water”. Catal. Sci. Technol. 2014, 4, 746–751. DOI: https://doi.org/10.1039/c3cy00831b.
- Gurrentz, J. M.; Rose, M. J. Non-Catalytic Benefits of Ni(II) Binding to an Si(111)-PNP Construct for Photoelectrochemical Hydrogen Evolution Reaction: Metal Ion Induced Flat Band Potential Modulation. J. Am. Chem. Soc. 2020, 142, 5657–5667. DOI: https://doi.org/10.1021/jacs.9b12824.
- Rosario-Amorinâ, D.; Wangâ, X.; Gaboyard, M.; Clérac, R.; Nlate, S.; Heuzé, K. Dendron-Functionalized Core–Shell Superparamagnetic Nanoparticles: Magnetically Recoverable and Reusable Catalysts for Suzuki C-C Cross-Coupling Reactions. Chem. Eur. J. 2009, 15, 12636–12643. DOI: https://doi.org/10.1002/chem.200901866.
- Rosario-Amorin, D.; Gaboyard, M.; Clérac, R.; Nlate, S.; Heuzé, K. Enhanced Catalyst Recovery in an Aqueous Copper-Free Sonogashira Cross-Coupling Reaction. Dalton Trans. 2011, 40, 44–46. DOI: https://doi.org/10.1039/C0DT01204A.
- Rosario-Amorin, D.; Gaboyard, M.; Clérac, R.; Vellutini, L.; Nlate, S.; Heuzé, K. Metallodendritic Grafted Core–Shell γ-Fe2O3 Nanoparticles Used as Recoverable Catalysts in Suzuki C-C Coupling Reactions. Chem. Eur. J. 2012, 18, 3305–3315. DOI: https://doi.org/10.1002/chem.201103147.
- Reetz, M. T.; Lohmer, G.; Schwickardi, R. Systhesis and Catalytic Activity of Dendritic Diphosphane Metal Complexes. Angew. Chem. Int. Ed. 1997, 36, 1526–1529. DOI: https://doi.org/10.1002/anie.199715261.
- Alonso, E.; Astruc, D. Introduction of the Cluster Fragment Ru3(CO)11 at the Periphery of Phosphine Dendrimers Catalyzed by the Electron-Reservoir Complex [FeICp(C6Me6)]. J. Am. Chem. Soc. 2000, 122, 3222–3223. DOI: https://doi.org/10.1021/ja994332j.
- Mizugaki, T.; Murata, M.; Ooe, M.; Ebitani, K.; Kaneda, K. Novel Catalysis of Dendrimer-Bound Pd(0) Complexes: Sterically Steered Allylic Amination and the First Application for a Thermomorphic System. Chem. Commun. 2002, 52–53. DOI: https://doi.org/10.1039/b107452k.
- Heuzé, K.; Méry, D.; Gauss, D.; Astruc, D. Copper-Free, Recoverable Dendritic Pd Catalysts for the Sonogashira Reaction. Chem. Commun. 2003, 2274–2275. DOI: https://doi.org/10.1039/B307116M.
- Feeder, N.; Geng, J.; Goh, P. G.; Johnson, B. F. G.; Martin, C. M.; Shephard, D. S.; Zhou, W. Nanoscale Super Clusters of Clusters Assembled around a Dendritic Core. Angew. Chem. Int. Ed. 2000, 39, 1661–1664. DOI: https://doi.org/10.1002/(SICI)1521-3773(20000502)39:9 < 1661::AID-ANIE1661 > 3.0.CO;2-H.
- Corzana, F.; Monge, M.; Sánchez-Forcada, E. Size and Shape Assessment of Organometallic Gold(I) Metallodendrimers through PGSE-NMR and Molecular Dynamics Simulations. Inorg. Chim. Acta 2012, 380, 31–39. DOI: https://doi.org/10.1016/j.ica.2011.10.006.
- Ujam, O. T.; Devey, K.; Henderson, W.; Nicholson, B. K.; Mucalo, M. R.; Decker, C.; Hor, T. S. A. Immobilization of [Pt2(μ-S)2(PPh3)4] on Polymeric Supports by Sulfide Alkylation and Phosphine Exchange Reactions. Phosphorus Sulfur Silicon Relat. Elem 2013, 188, 1508–1525. DOI: https://doi.org/10.1080/10426507.2012.761990.
- Arya, P.; Rao, N. V.; Singkhonrat, J.; Alper, H.; Bourque, S. C.; Manzer, L. E. A Divergent, Solid-Phase Approach to Dendritic Ligands on Beads. Heterogeneous Catalysis for Hydroformylation Reactions. J. Org. Chem. 2000, 65, 1881–1885. DOI: https://doi.org/10.1021/jo991621h.
- Arya, P.; Panda, G.; Rao, N. V.; Alper, H.; Bourque, S. C.; Manzer, L. E. Solid-Phase Catalysis: A Biomimetic Approach toward Ligands on Dendritic Arms to Explore Recyclable Hydroformylation reactions. J. Am. Chem. Soc. 2001, 123, 2889–2890. DOI: https://doi.org/10.1021/ja003854s.
- Lu, S.-M.; Alper, H. Hydroformylation Reactions with Recyclable Rhodium-Complexed Dendrimers on a Resin. J. Am. Chem. Soc. 2003, 125, 13126–13131. DOI: https://doi.org/10.1021/ja0303384.
- Lu, S.-M.; Alper, H. Carbonylative Ring Expansion of Aziridines to β-Lactams with Rhodium-Complexed Dendrimers on a Resin. J. Org. Chem. 2004, 69, 3558–3561. DOI: https://doi.org/10.1021/jo030353r.
- Gottis, S.; Rodriguez, L.-I.; Laurent, R.; Angurell, I.; Seco, M.; Rossell, O.; Majoral, J.-P.; Caminade, A.-M. Janus Carbosilane/Phosphorhydrazone Dendrimers Synthesized by the ‘Click’ Staudinger Reaction. Tetrahedron Lett. 2013, 54, 6864–6867. DOI: https://doi.org/10.1016/j.tetlet.2013.10.024.
- Posset, T.; Blümel, J. New Mechanistic Insights regarding Pd/Cu Catalysts for the Sonogashira Reaction: HRMAS NMR Studies of Silica-Immobilized Systems. J. Am. Chem. Soc. 2006, 128, 8394–8395. DOI: https://doi.org/10.1021/ja062206r.
- You, S.; Huang, B.; Yan, T.; Cai, M. A Highly Efficient Heterogeneous Palladium-Catalyzed Carbonylative Annulation of 2-Aminobenzamides with Aryl Iodides Leading to Quinazolinones. J. Organomet. Chem. 2018, 875, 35–45. DOI: https://doi.org/10.1016/j.jorganchem.2018.09.003.
- Xu, Z.; Huang, B.; Zhou, Z.; Cai, M. Recyclable Heterogeneous Palladium-Catalyzed Carbonylative Cyclization of 2-Iodoanilines with Aryl Iodides Leading to 2-Arylbenzoxazinones. Synthesis 2020, 52, 581–590. DOI: https://doi.org/10.1055/s-0039-1690265.
- Motokura, K.; Saitoh, K.; Noda, H.; Chun, W.-J.; Miyaji, A.; Yamaguchi, S.; Baba, T. A. Pd–Bisphosphine Complex and Organic Functionalities Immobilized on the Same SiO2 Surface: Detailed Characterization and Its Use as an Efficient Catalyst for Allylation. Catal. Sci. Technol. 2016, 6, 5380–5388. DOI: https://doi.org/10.1039/C6CY00593D.
- Motokura, K.; Ikeda, M.; Kim, M.; Nakajima, K.; Kawashima, S.; Nambo, M.; Chun, W. J.; Tanaka, S. Silica Support‐Enhanced Pd‐Catalyzed Allylation Using Allylic Alcohols. ChemCatChem 2018, 10, 4536–4544. DOI: https://doi.org/10.1002/cctc.201801097.
- Motokura, K.; Fukuda, T.; Uemura, Y.; Matsumura, D.; Ikeda, M.; Nambo, M.; Chun, W.-J. Effects of Mesopore Internal Surfaces on the Structure of Immobilized Pd-Bisphosphine Complexes Analyzed by Variable-Temperature XAFS and Their Catalytic Performances. Catalysts 2018, 8, 106. DOI: https://doi.org/10.3390/catal8030106.
- Motokura, K.; Kawashima, S.; Nambo, M.; Manaka, Y.; Chun, W. J. Accumulation of Active Species in Silica Mesopore: Effect of the Pore Size and Free Base Additives on Pd‐Catalyzed Allylation Using Allylic Alcohol. ChemCatChem 2020, 12, 2783–2791. DOI: https://doi.org/10.1002/cctc.202000266.
- Cai, M.; Sha, J.; Xu, Q. MCM-41-Supported Bidentate Phosphine Palladium(0) Complex: A Highly Active and Recyclable Catalyst for the Sonogashira Reaction of Aryl Iodides. Tetrahedron 2007, 63, 4642–4647. DOI: https://doi.org/10.1016/j.tet.2007.03.111.
- Cai, M.; Sha, J.; Xu, Q. MCM-41-Supported Bidentate Phosphine Palladium(0) Complex as an Efficient Catalyst for the Heterogeneous Suzuki Reaction. J. Mol. Catal. A: Chem. 2007, 268, 82–86. DOI: https://doi.org/10.1016/j.molcata.2006.12.011.
- Cai, M.; Sha, J. Diphosphino-Functionalized MCM-41 Anchored Palladium(0) Complex as an Efficient Catalyst for Heck Arylation of Conjugated Alkenes with Aryl Halides. Catal. Commun. 2007, 8, 1691–1696. DOI: https://doi.org/10.1016/j.catcom.2007.01.038.
- Jin, M.-J.; Sarkar, M. S.; Lee, D.-H.; Lee, I.-M. Mesoporous Silica SBA-15-Supported Palladium Catalyst for Green Sonogashira Coupling Reactions. Stud. Surf. Sci. Catal. 2007, 165, 709–712. DOI: https://doi.org/10.1016/S0167-2991(07)80419-8.
- Hao, W.; Sha, J.; Sheng, S.; Cai, M. The First Heterogeneous Carbonylative Sonogashira Coupling Reaction Catalyzed by MCM-41-Supported Bidentate Phosphine Palladium(0) Complex. J. Mol. Catal. A: Chem. 2009, 298, 94–98. DOI: https://doi.org/10.1016/j.molcata.2008.09.031.
- Cao, M.; Wang, Z.; Zhang, J.; Xu, S.; Zhang, S.; Da, X.; Jiang, X. Preparation, Characterization and Photocatalytic Properties of Diiron Mimic Modified Nano Silica. Inorg. Chim. Acta 2018, 469, 402–407. DOI: https://doi.org/10.1016/j.ica.2017.09.007.
- Hao, W.; Sha, J.; Sheng, S.; Cai, M. MCM-41-Supported Bidentate Phosphine Palladium(II) Complex as an Efficient Catalyst for the Carbonylation of Aryl Halides. Catal. Commun. 2008, 10, 257–260. DOI: https://doi.org/10.1016/j.catcom.2008.09.004.
- Cai, M.; Zheng, G.; Ding, G. The First Heterogeneous Carbonylative Stille Coupling of Organostannanes with Aryl Iodides Catalyzed by MCM-41-Supported Bidentate Phosphine Palladium(0) Complex. Green Chem. 2009, 11, 1687–1693. DOI: https://doi.org/10.1039/b914844m.
- Zhao, H.; Zheng, G.; Sheng, S.; Cai, M. Carbonylative Cross-Coupling of Aryl Halides with Sodium Tetraphenylborate Catalyzed by MCM-41-Supported Bidentate Phosphine Palladium(II) Complex. Catal. Commun. 2009, 11, 158–161. DOI: https://doi.org/10.1016/j.catcom.2009.09.016.
- Cai, M.; Zheng, G.; Zha, L.; Peng, J. Carbonylative Suzuki–Miyaura Coupling of Arylboronic Acids with Aryl Iodides Catalyzed by the MCM‐41‐Supported Bidentate Phosphane Palladium(II) Complex. Eur. J. Org. Chem. 2009, 1585–1591. DOI: https://doi.org/10.1002/ejoc.200801253.
- Zheng, G.; Wang, P.; Cai, M. A New Route to Biaryl Ketones via Carbonylative Suzuki Coupling Catalyzed by MCM-41-Supported Bidentate Phosphine Palladium(0) Complex. Chin. J. Chem. 2009, 27, 1420–1426. DOI: https://doi.org/10.1002/cjoc.200990239.
- Wang, Y.; Huang, B.; Sheng, S.; Cai, M. A Novel and Efficient Synthesis of Terminal Arylacetylenes via Sonogashira Coupling Reactions Catalysed by MCM-41-Supported Bidentate Phosphine Palladium(0) Complex. J. Chem. Res. 2007, 2007, 728–732. DOI: https://doi.org/10.3184/030823407X275928.
- Zhao, H.; Wang, Y.; Sha, J.; Sheng, S.; Cai, M. MCM-41-Supported Bidentate Phosphine Palladium(0) Complex as an Efficient Catalyst for the Heterogeneous Stille Reaction. Tetrahedron 2008, 64, 7517–7523. DOI: https://doi.org/10.1016/j.tet.2008.05.120.
- Jiang, J.; Wang, P.; Cai, M. Diphosphino-Functionalised MCM-41-Supported Palladium Complex: An Efficient and Recyclable Catalyst for the Formylation of Aryl Halides. J. Chem. Res. 2014, 38, 218–222. DOI: https://doi.org/10.3184/174751914X13934116089943.
- Zhou, Z.; Huang, B.; Cai, M. Recyclable Palladium-Catalyzed Carbonylative Annulation of 2-Iodoanilines with Acid Anhydrides: A Practical Synthesis of 2-Alkylbenzoxazinones. Synth. Commun. 2021, 51, 3150–3163. DOI: https://doi.org/10.1080/00397911.2021.1966039.
- Zha, L.; Hao, W.; Cai, M. A Diphosphino-Functionalised MCM-41-Anchored Platinum Complex: An Efficient and Reusable Catalyst for the Hydrosilylation of Olefins. J. Chem. Res. 2010, 34, 648–652. DOI: https://doi.org/10.3184/030823410X12887259824283.
- Xia, J.; Yao, R.; Cai, M. A Highly Efficient Heterogeneous Rhodium(I)‐Catalyzed C–S Coupling Reaction of Thiols with Polychloroalkanes or Alkyl Halides under Mild Conditions. Appl. Organometal. Chem. 2015, 29, 221–225. DOI: https://doi.org/10.1002/aoc.3273.
- Zhao, H.; Peng, J.; Cai, M. Heterogeneous Hydrothiolation of Alkynes with Thiols Catalyzed by Diphosphino-Functionalized MCM-41 Anchored Rhodium Complex. Catal. Lett. 2012, 142, 138–142. DOI: https://doi.org/10.1007/s10562-011-0732-x.
- Bourque, S. C.; Maltais, F.; Xiao, W.-J.; Tardif, O.; Alper, H.; Arya, P.; Manzer, L. E. Hydroformylation Reactions with Rhodium-Complexed Dendrimers on Silica. J. Am. Chem. Soc. 1999, 121, 3035–3038. DOI: https://doi.org/10.1021/ja983764b.
- Lu, S.-M.; Alper, H. Intramolecular Carbonylation Reactions with Recyclable Palladium-Complexed Dendrimers on Silica: Synthesis of Oxygen, Nitrogen, or Sulfur-Containing Medium Ring Fused Heterocycles. J. Am. Chem. Soc. 2005, 127, 14776–14784. DOI: https://doi.org/10.1021/ja053650h.
- Bourque, S. C.; Alper, H. Hydroformylation Reactions Using Recyclable Rhodium-Complexed Dendrimers on Silica. J. Am. Chem. Soc. 2000, 122, 956–957. DOI: https://doi.org/10.1021/ja993196f.
- Reynhardt, J. P. K.; Yang, Y.; Sayari, A.; Alper, H. Periodic Mesoporous Silica-Supported Recyclable Rhodium-Complexed Dendrimer Catalysts. Chem. Mater. 2004, 16, 4095–4102. DOI: https://doi.org/10.1021/cm0493142.
- Reynhardt, J. P. K.; Yang, Y.; Sayari, A.; Alper, H. Rhodium Complexed C2‐PAMAM Dendrimers Supported on Large Pore Davisil Silica as Catalysts for the Hydroformylation of Olefins. Adv. Synth. Catal. 2005, 347, 1379–1388. DOI: https://doi.org/10.1002/adsc.200505065.
- Alper, H.; Arya, P.; Bourque, S. C.; Jefferson, G. R.; Manzer, L. E. Heck Reaction Using Palladium Complexed to Dendrimers on Silica. Can. J. Chem. 2000, 78, 920–924. DOI: https://doi.org/10.1139/v00-018.
- Antebi, S.; Arya, P.; Manzer, L. E.; Alper, H. Carbonylation Reactions of Iodoarenes with PAMAM Dendrimer-Palladium Catalysts Immobilized on Silica. J. Org. Chem. 2002, 67, 6623–6631. DOI: https://doi.org/10.1021/jo020271n.
- Touzani, R.; Alper, H. PAMAM Dendrimer-Palladium Complex Catalyzed Synthesis of Five-, Six- or Seven Membered Ring Lactones and Lactams by Cyclocarbonylation Methodology. J. Mol. Catal. A: Chem. 2005, 227, 197–207. DOI: https://doi.org/10.1016/j.molcata.2004.10.024.
- Lu, S. M.; Alper, H. Synthesis of Large Ring Macrocycles (12-18) by Recyclable Palladium-Complexed Dendrimers on Silica Gel Catalyzed Intramolecular Cyclocarbonylation Reactions. Chemistry 2007, 13, 5908–5916. DOI: https://doi.org/10.1002/chem.200601724.
- Zweni, P. P.; Alper, H. Silica-Supported Dendrimer-Palladium Complex-Catalyzed Selective Hydrogenation of Dienes to Monoolefins. Adv. Synth. Catal. 2006, 348, 725–731. DOI: https://doi.org/10.1002/adsc.200505236.
- Tang, H.; Huang, B.; Zhu, X.; Cai, M. Synthesis of Poly(Ether Ketone Amide)s Containing 4‐Aryl‐2,6‐Diphenylpyridine Moieties by a Heterogeneous Palladium‐Catalyzed Polycondensation of Aromatic Diiodides, Aromatic Diamines, and Carbon Monoxide. Polym. Adv. Technol. 2018, 29, 2204–2215. DOI: https://doi.org/10.1002/pat.4328.
- Huang, B.; Wang, P.; Zhu, X.; Cai, M. Synthesis of Poly(Ether Ketone Amide)s by a Heterogeneous Palladium-Catalyzed Polycondensation of Aromatic Diiodides, Diamines, and Carbon Monoxide. High Perform. Polym. 2019, 31, 425–437. DOI: https://doi.org/10.1177/0954008318781700.
- Liu, L.; Zou, F.; Zhang, R.; Cai, M. Synthesis of New Fluorinated Aromatic Poly (Ether Ketone Amide)s Containing Cardo Structures by a Heterogeneous Palladium‐Catalyzed Carbonylative Polycondensation. Polym. Adv. Technol. 2019, 30, 58–69. DOI: https://doi.org/10.1002/pat.4443.
- Zou, F.; Huang, B.; Liu, L.; Cai, M. Synthesis of Cardo Poly(Arylene Ether Ketone Amide)s by Heterogeneous Palladium-Catalyzed Polycondensation of Aromatic Diiodides, Aromatic Diamines Containing Cardo Groups and CO. Polym. Bull. 2020, 77, 1983–2001. DOI: https://doi.org/10.1007/s00289-019-02844-6.
- Liu, L.; Li, J.; Yan, T.; Cai, M. Novel Preparation of Poly(Arylene Ether Sulfone Amide)s via Supported Palladium-Catalyzed Carbonylative Polymerization. Polym. Bull. 2020, 77, 1951–1968. DOI: https://doi.org/10.1007/s00289-019-02843-7.
- Zou, F.; Yao, F.; Liu, L.; Cai, M. Recyclable Heterogeneous Palladium-Catalyzed Carbon–Carbon Coupling Polycondensations toward Highly Purified Conjugated Polymers. J. Polym. Res. 2020, 27, 1. DOI: https://doi.org/10.1007/s10965-019-1979-y.
- Tang, H.; Yao, F.; Liu, L.; Cai, M. Recyclable Heterogeneous Palladium-Catalyzed Heck Coupling Polycondensation of Bis(Acrylamide)s with Aromatic Diiodides towards Polycinnamamides. J. Macromol. Sci. A 2020, 57, 198–206. DOI: https://doi.org/10.1080/10601325.2019.1680256.
- You, S.; Yan, C.; Zhang, R.; Cai, M. A Convenient and Practical Heterogeneous Palladium-Catalyzed Carbonylative Suzuki Coupling of Aryl Iodides with Formic Acid as Carbon Monoxide Source. Appl. Organomet. Chem. 2019, 33, id: 4650. DOI: https://doi.org/10.1002/aoc.4650.
- Li, J.; Huang, B.; Tang, H.; Cai, M. Synthesis and Characterization of Novel Soluble Poly(Arylene Ether Amide Triphenylphosphine Oxide)s by Heterogeneous Palladium-Catalyzed Carbonylation Polymerization. J. Macromol. Sci. A 2020, 57, 896–905. DOI: https://doi.org/10.1080/10601325.2020.1810067.
- Natour, S.; Abu-Reziq, R. Functionalized Magnetic Mesoporous Silica Nanoparticle-Supported Palladium Catalysts for Carbonylative Sonogashira Coupling Reactions of Aryl Iodides. ChemCatChem 2015, 7, 2230–2240. DOI: https://doi.org/10.1002/cctc.201500356.
- Uruş, S. Synthesis of Fe3O4@SiO2@OSi(CH2)3NHRN(CH2PPh2)2 PdCl2 Type Nanocomposite Complexes: Highly Efficient and Magnetically-Recoverable Catalysts in Vitamin K3 Synthesis. Food Chem. 2016, 213, 336–343. DOI: https://doi.org/10.1016/j.foodchem.2016.06.093.
- Abu-Reziq, R.; Alper, H.; Wang, D.; Post, M. L. Metal Supported on Dendronized Magnetic Nanoparticles: Highly Selective Hydroformylation Catalysts. J. Am. Chem. Soc. 2006, 128, 5279–5282. DOI: https://doi.org/10.1021/ja060140u.
- Uruş, S.; Eskalen, H.; Çaylar, M.; Akbulut, M. Highly Effective Aldose Reductase Mimetics: Microwave-Assisted Catalytic Transfer Hydrogenation of D-Glucose to D-Sorbitol with Magnetically Recoverable Aminomethylphosphine-Ru(II) and Ni(II) Complexes. J. Mol. Struct. 2021, 1237, id: 130313. DOI: https://doi.org/10.1016/j.molstruc.2021.130313
- Shaikh, M. N.; Bououdina, M.; Jimoh, A. A.; Aziz, M. A.; Helal, A.; Hakeem, A. S.; Yamani, Z. H.; Kim, T.-J. The Rhodium Complex of Bis(Diphenylphosphinomethyl)Dopamine-Coated Magnetic Nanoparticles as an Efficient and Reusable Catalyst for Hydroformylation of Olefins. New J. Chem. 2015, 39, 7293–7299. DOI: https://doi.org/10.1039/C5NJ01170A.
- Shaikh, M. N.; Yamani, Z. H. Surface Bonded Rh-Bis(diarylphosphine) on Magnetic Nanoparticles as a Recyclable Catalyst for Hydroformylation of Olefins. U.S. Patent 9,480,978, Nov 1, 2016.
- Henderson, W.; Olsen, G. M.; Bonnington, L. S. Immobilised Phosphines Incorporating the Chiral Biopolymers Chitosan and Chitin. J. Chem. Soc, Chem. Commun. 1994, 1863–1864. DOI: https://doi.org/10.1039/c39940001863.
- Cao, M.; Wang, Z.; Yuan, Z.; Jiang, X.; Xu, S.; Liu, Y.; Zhang, S.; Dai, X. Synthesis and Photocatalytic Properties of Two Different Chitosan-Based Structural Hydrogenase Models. Inorg. Chem. Commun. 2019, 103, 128–135. DOI: https://doi.org/10.1016/j.inoche.2019.03.015.
- Willocq, C.; Hermans, S.; Devillers, M. Active Carbon Functionalized with Chelating Phosphine Groups for the Grafting of Model Ru and Pd Coordination Compounds. J. Phys. Chem. C. 2008, 112, 5533–5541. DOI: https://doi.org/10.1021/jp076799j.
- Willocq, C.; Dubois, V.; Khimyak, Y. Z.; Devillers, M.; Hermans, S. Hydrogenation of Nitrobenzene over Pd/C Catalysts Prepared from Molecular Carbonyl–Phosphine Palladium Clusters. J. Mol. Catal. A: Chem. 2012, 365, 172–180. DOI: https://doi.org/10.1016/j.molcata.2012.09.001.
- Uruş, S.; Çaylar, M.; Karteri, İ. Synthesis of Graphene Supported Bis(Diphenylphosphinomethyl)Amino Ligands and Their Pd(II) and Pt(II) Complexes: Highly Efficient and Recoverable Nano-Catalysts on Vitamin K3 Production. Chem. Eng. J. 2016, 306, 961–972. DOI: https://doi.org/10.1016/j.cej.2016.08.009.
- Vidick, D.; Herlitschke, M.; Poleunis, C.; Delcorte, A.; Hermann, R. P.; Devillers, M.; Hermans, S. Comparison of Functionalized Carbon Nanofibers and Multi-Walled Carbon Nanotubes as Supports for Fe–Co Nanoparticles. J. Mater. Chem. A 2013, 1, 2050–2063. DOI: https://doi.org/10.1039/C2TA00131D.
- Uruş, S.; Adıgüzel, H.; Keleş, M.; Karteri, İ. Multi-Walled Carbon Nanotube Supported Aminomethylphosphine-Ru(II) Complexes: Optical Behavior and Catalytic Properties in Transfer Hydrogenation of Acetophenone Derivatives. Fuller. Nanotub. Carbon Nanostruct. 2017, 25, 133–141. DOI: https://doi.org/10.1080/1536383X.2016.1271789.
- Uruş, S.; Adıgüzel, H.; Keleş, M.; Karteri, İ. Pincer Type Ditertiary Aminomethylphosphine–Pd(II) Complexes Supported on Multi-Walled Carbon Nanotube: Catalytic Properties in Heck C–C Coupling Reactions. J. Inorg. Organomet. Polym. 2017, 27, 138–145. DOI: https://doi.org/10.1007/s10904-017-0642-5.
- Vidick, D.; Leonard, A. F.; Poleunis, C.; Delcorte, A.; Devillers, M.; Hermans, S. Phosphine- and Ammonium-Functionalized Ordered Mesoporous Carbons as Supports for Cluster-Derived Metal Nanoparticles. Catal. Today 2014, 235, 112–126. DOI: https://doi.org/10.1016/j.cattod.2014.03.017.
- Gonthier, E.; Breinbauer, R. An Easily Accessible Resin-Supported Palladium Catalyst for Sonogashira Coupling. Synlett 2003, 1049–1051. DOI: https://doi.org/10.1055/s-2003-39305.
- Brehm, E.; Breinbauer, R. Investigation of the Origin and Synthetic Application of the Pseudodilution Effect for Pd-Catalyzed Macrocyclisations in Concentrated Solutions with Immobilized Catalysts. Org. Biomol. Chem. 2013, 11, 4750–4756. DOI: https://doi.org/10.1039/c3ob41020j.
- Westhus, M.; Gonthier, E.; Brohm, D.; Breinbauer, R. An Efficient and Inexpensive Scavenger Resin for Grubbs’ Catalyst. Tetrahedron Lett. 2004, 45, 3141–3142. DOI: https://doi.org/10.1016/j.tetlet.2004.02.083.
- Judkins, C. M. G.; Knights, K. A.; Johnson, B. F. G.; de Miguel, Y. R.; Raja, R.; Thomas, J. M. Immobilisation of Ruthenium Cluster Catalysts via Novel Derivatisations of ArgoGel Resins. Chem. Commun. 2001, 2624–2625. DOI: https://doi.org/10.1039/b106336g.
- Uozumi, Y.; Nakai, Y. An Amphiphilic Resin-Supported Palladium Catalyst for High-Throughput Cross-Coupling in Water. Org. Lett. 2002, 4, 2997–3000. DOI: https://doi.org/10.1021/ol0264298.
- Judkins, C. M. G.; Knights, K. A.; Johnson, B. F. G.; de Miguel, Y. R. Gas Sensor Activity of ArgoGel Resin-Supported Pentaruthenium Clusters. Polyhedron 2003, 22, 3–7. DOI: https://doi.org/10.1016/S0277-5387(02)01325-6.
- Issleib, K.; Oehme, H. Alkali-Phosphorverbindungen und Ihr Reaktives Verhalten. LI. Synthese und Reaktionsverhalten des [β-Amino-Äthyl]-Phenyl-Phosphins. Chem. Ber. 1967, 100, 2685–2693. DOI: https://doi.org/10.1002/cber.19671000832.
- Issieib, K.; Oehme, H. Phosphazolidine. Tetrahedron Lett. 1967, 8, 1489–1492. DOI: https://doi.org/10.1016/S0040-4039(00)90987-0.
- Issleib, K.; Oehme, H.; Leißring, E. Perhydro-1.3-Azaphosphorine. Chem. Ber. 1968, 101, 4032–4035. DOI: https://doi.org/10.1002/cber.19681011204.
- Scherhag, G.; Spicer, M. D. Preparation of a Cyclic Trimer with a Ni3P3 Core: Aggregation and Conformation Driven by Steric Demand. J. Chem. Soc, Dalton Trans. 2000, 1237–1238. DOI: https://doi.org/10.1039/b001098g.
- Issleib, K.; Oehme, H. Zur Kondensation Sek.-4-Aminobutylphosphine mit Aldehyden und Ketonen. Z Chem. 2010, 13, 139–141. DOI: https://doi.org/10.1002/zfch.19730130414.
- Issleib, K. Element-Phosphor-Heterocyclen. Phosphorus Sulfur Silicon Relat. Elem. 1976, 2, 219–235. DOI: https://doi.org/10.1080/03086647608078954.
- Collins, D. J.; Drygala, P. F.; Swan, J. M. Organophosphorus Compounds. XVIII. Synthesis of 2-Phenyl-2,3-Dihydro-1H-1,2-Benzazaphosphole 2-Sulfide by Pyrolysis of (2-Aminobenzyl)Phenyldithiophosphinic Acid. Aust. J. Chem. 1983, 36, 2095–2110. DOI: https://doi.org/10.1071/CH9832095.
- Dey, S.; Sun, W.; Müller, J. [n]Ferrocenophanes (n = 2, 3) with Nitrogen and Phosphorus in Bridging Positions. Inorg. Chem. 2016, 55, 3630–3639. DOI: https://doi.org/10.1021/acs.inorgchem.6b00170.
- Heinicke, J.; Tzschach, A. Zur Synthese der 1,3-Azaphospholine-1. Z Chem. 2010, 26, 407–408. DOI: https://doi.org/10.1002/zfch.19860261115.
- Karasik, A. A.; Bobrov, S. V.; Akhmetzyanov, A. I.; Naumov, R. N.; Nikonov, G. N.; Sinyashin, O. G. Synthesis of 1-R-3,5-Diphenyl-1,3,5-Azadiphosphorinanes and Thier Platinum(II) and Palladium(II) Complexes. Koord. Khim. 1998, 24, 530–535.
- Musina, E. I.; Musin, L. I.; Litvinov, I. A.; Karasik, A. A. Synthesis of New 1,3,5-Azadiphosphorinanes Based on Aliphatic Amines. Russ. J. Gen. Chem. 2020, 90, 224–228. DOI: https://doi.org/10.1134/S1070363220020097.
- Wittmann, T. I. New 14-Membered Cyclic Tetrakisphosphines and Their Complexes with Transition Metals: Synthesis and Behavior in Solutions. Ph.D. Dissertation, A. E. Arbuzov Institute of Organic and Physical Chemistry, Russian Federation, Kazan, 2015.
- Musina, E. I.; Karasik, A. A.; Balueva, A. S.; Strelnik, I. D.; Fesenko, T. I.; Dobrynin, A. B.; Gerasimova, T. P.; Katsyuba, S. A.; Kataeva, O. N.; Lönnecke, P.; et al. Synthesis and Stereoselective Interconversion of Chiral 1‐Aza‐3,6‐Diphosphacycloheptanes. Eur. J. Inorg. Chem. 2012, 1857–1866. DOI: https://doi.org/10.1002/ejic.201101337.
- Karasik, A. A.; Balueva, A. S.; Moussina, E. I.; Naumov, R. N.; Dobrynin, A. B.; Krivolapov, D. B.; Litvinov, I. A.; Sinyashin, O. G. 1,3,6-Azadiphosphacycloheptanes: A Novel Type of Heterocyclic Diphosphines. Heteroatom Chem. 2008, 19, 125–132. DOI: https://doi.org/10.1002/hc.20397.
- Brown, H. J. S.; Wiese, S.; Roberts, J. A. S.; Bullock, R. M.; Helm, M. L. Electrocatalytic Hydrogen Production by [Ni(7PPh2NH)2]2+: Removing the Distinction between Endo- and Exo-Protonation Sites. ACS Catal. 2015, 5, 2116–2123. DOI: https://doi.org/10.1021/cs502132y.
- Fesenko, T. I.; Strelnik, I. D.; Musina, E. I.; Karasik, A. A.; Sinyashin, O. G. Synthesis of 1-(Pyridylalkyl)-1-Aza-3,6-Diphosphacycloheptanes. Russ. Chem. Bull. 2012, 61, 1792–1797. DOI: https://doi.org/10.1007/s11172-012-0247-7.
- Stewart, M. P.; Ho, M.-H.; Wiese, S.; Lindstrom, M. L.; Thogerson, C. E.; Raugei, S.; Bullock, R. M.; Helm, M. L. High Catalytic Rates for Hydrogen Production Using Nickel Electrocatalysts with Seven-Membered Cyclic Diphosphine Ligands Containing One Pendant Amine. J. Am. Chem. Soc. 2013, 135, 6033–6046. DOI: https://doi.org/10.1021/ja400181a.
- Reback, M. L.; Buchko, G. W.; Kier, B. L.; Ginovska-Pangovska, B.; Xiong, Y.; Lense, S.; Hou, J.; Roberts, J. A. S.; Sorensen, C. M.; Raugei, S.; et al. Enzyme Design from the Bottom up: An Active Nickel Electrocatalyst with a Structured Peptide Outer Coordination Sphere. Chemistry 2014, 20, 1510–1514. DOI: https://doi.org/10.1002/chem.201303976.
- Reback, M. L.; Ginovska, B.; Buchko, G. W.; Dutta, A.; Priyadarshani, N.; Kier, B. L.; Helm, M. L.; Raugei, S.; Shaw, W. J. Investigating the Role of Chain and Linker Length on the Catalytic Activity of an H2 Production Catalyst Containing a β-Hairpin Peptide. J. Coord. Chem. 2016, 69, 1730–1747. DOI: https://doi.org/10.1080/00958972.2016.1188924.
- Musina, E. I.; Wittmann, T. I.; Strelnik, I. D.; Naumova, O. E.; Karasik, A. A.; Krivolapov, D. B.; Islamov, D. R.; Kataeva, O. N.; Sinyashin, O. G.; Lönnecke, P.; Hey-Hawkins, E. Influence of the Rac–Meso Isomerization of Seven-Membered Cyclic Bisphosphines on the Predominant Formation of Chelate Complexes. Polyhedron 2015, 100, 344–350. DOI: https://doi.org/10.1016/j.poly.2015.08.033.
- Wiese, S.; Kilgore, U. J.; Ho, M.-H.; Raugei, S.; DuBois, D. L.; Bullock, R. M.; Helm, M. L. Hydrogen Production Using Nickel Electrocatalysts with Pendant Amines: Ligand Effects on Rates and Overpotentials. ACS Catal. 2013, 3, 2527–2535. DOI: https://doi.org/10.1021/cs400638f.
- Karasik, A. A.; Naumov, R. N.; Spiridonova, Y. S.; Sinyashin, O. G.; Lönnecke, P.; Hey-Hawkins, E. Synthesis, Molecular Structure and Coordination Chemistry of the First 1‐Aza‐3,7‐Diphosphacyclooctanes. Z. Anorg. Allg. Chem. 2007, 633, 205–210. DOI: https://doi.org/10.1002/zaac.200600227.
- Stolley, R. M.; Darmon, J. M.; Das, P.; Helm, M. L. Nickel Bis-Diphosphine Complexes: Controlling the Binding and Heterolysis of H2. Organometallics 2016, 35, 2965–2974. DOI: https://doi.org/10.1021/acs.organomet.6b00486.
- Kreienbrink, A.; Lönnecke, P.; Findeisen, M.; Hey-Hawkins, E. Hey-Hawkins, E. Endocyclic P–P Bond Cleavage in Carbaborane-Substituted 1,2-Diphosphetane: A New Route to Secondary Phosphinocarbaboranes. Chem. Commun. 2012, 48, 9385–9387. DOI: https://doi.org/10.1039/c2cc34860h.
- Musina, E. I.; Fesenko, T. I.; Strelnik, I. D.; Polyancev, F. M.; Latypov, S. K.; Lönnecke, P.; Hey-Hawkins, E.; Karasik, A. A.; Sinyashin, O. G. Synthesis and Unique Reversible Splitting of 14-Membered Cyclic Aminomethylphosphines on to 7-Membered Heterocycles. Dalton Trans. 2015, 44, 13565–13572. DOI: https://doi.org/10.1039/C5DT01910A.
- Musina, E. I.; Naumov, R. N.; Kanunnikov, K. B.; Dobrynin, A. B.; Gómez-Ruiz, S.; Lönnecke, P.; Hey-Hawkins, E.; Karasik, A. A.; Sinyashin, O. G. Chiral [16]-Ane P4N2 Macrocycles: Stereoselective Synthesis and Unexpected Intermolecular Exchange of Endocyclic Fragments. Dalton Trans. 2018, 47, 16977–16984. DOI: https://doi.org/10.1039/C8DT03214A.
- Musina, E.; Wittmann, T.; Latypov, S.; Kondrashova, S.; Lönnecke, P.; Litvinov, I.; Hey-Hawkins, E.; Karasik, A. Self-Assembly of Chiral 1,8-Diaza-3,6,10,13-Tetraphosphacyclotetradecanes via Dynamic Transformation of 7- and 14-Membered Aminomethylphosphines. Eur. J. Inorg. Chem. 2019, 3053–3060. DOI: https://doi.org/10.1002/ejic.201900386.
- Musina, E. I.; Wittmann, T. I.; Musin, L. I.; Balueva, A. S.; Shpagina, A. S.; Litvinov, I. A.; Lönnecke, P.; Hey-Hawkins, E.; Karasik, A. A.; Sinyashin, O. G. Dynamic Covalent Chemistry Approach toward 18-Membered P4N2 Macrocycles and Their Nickel(II) Complexes. J. Org. Chem. 2020, 85, 14610–14618. DOI: https://doi.org/10.1021/acs.joc.0c01317.
- Musina, E. I.; Karasik, A. A.; Strelnik, I. D.; Lönnecke, P.; Hey-Hawkins, E.; Sinyashin, O. G. First Example of 14-Membered Cyclic Aminomethylphosphine. Phosphorus Sulfur Silicon Relat. Elem. 2011, 186, 761–763. DOI: https://doi.org/10.1080/10426507.2010.506667.
- Wittmann, T. I.; Musina, E. I.; Krivolapov, D. B.; Litvinov, I. A.; Kondrashova, S. A.; Latypov, S. K.; Karasik, A. A.; Sinyashin, O. G. Covalent Self-Assembly of the Specific RSSR Isomer of 14-Membered Tetrakisphosphine. Dalton Trans. 2017, 46, 12417–12420. DOI: https://doi.org/10.1039/C7DT03010J.
- Wittmann, T. I.; Musina, E. I.; Karasik, A. A.; Sinyashin, O. G. Novel Chiral 14-Membered Aminomethylphosphines. Phosphorus Sulfur Silicon Relat. Elem. 2016, 191, 1533–1534. DOI: https://doi.org/10.1080/10426507.2016.1212857.
- Karasik, A. A.; Naumov, R. N.; Kanunnikov, K. B.; Krivolapov, D. B.; Litvinov, I. A.; Lönnecke, P.; Balueva, A. S.; Musina, E. I.; Hey-Hawkins, E.; Sinyashin, O. G. Synthesis of New Examples of Corands with 16-Membered P,N-Containing Core Ring. Macroheterocycles 2014, 7, 181–188. DOI: https://doi.org/10.6060/mhc140507b.
- Wittmann, T. I.; Musina, E. I.; Litvinov, I. A.; Karasik, A. A.; Sinyashin, O. G. Synthesis of a 16-Membered P4N2 Macrocycle with Pyridyl-Substituted Phosphorus Atoms. Russ. J. Gen. Chem. 2018, 88, 2449–2452. DOI: https://doi.org/10.1134/S1070363218110336.
- Naumov, R. N.; Karasik, A. A.; Kanunnikov, K. B.; Kozlov, A. V.; Latypov, S. K.; Domasevitch, K. V.; Hey-Hawkins, E.; Sinyashin, O. G. Synthesis of a Chiral Macrocyclic Tetraphosphine 1,9-Di-R,R(and S,S)-α-Methylbenzyl-3,7,11,15-Tetramesityl-1,9-Diaza-3,7,11,15-(RSSR)-Tetraphosphacyclohexadecane. Synthesis of a Chiral Macrocyclic Tetraph. Mendeleev Commun. 2008, 18, 80–81. DOI: https://doi.org/10.1016/j.mencom.2008.03.008.
- Musina, E. I.; Wittmann, T. I.; Lönnecke, P.; Hey-Hawkins, E.; Karasik, A. A.; Sinyashin, O. G. Novel Representatives of 16-Membered Aminomethylphosphines with Alkyl Substituents at Nitrogen and Their Gold(I) Complexes. Russ. Chem. Bull. 2018, 67, 328–335. DOI: https://doi.org/10.1007/s11172-018-2078-7.
- Naumov, R. N.; Karasik, A. A.; Sinyashin, O. G.; Lönnecke, P.; Hey-Hawkins, E. Unexpected Formation of a Novel Macrocyclic Tetraphosphine: (RSSR)-1,9-Dibenzyl-3,7,11,15-Tetramesityl-1,9-Diaza-3,7,11,15-Tetraphosphacyclohexadecane. Dalton Trans. 2004, 357–358. DOI: https://doi.org/10.1039/B313487C.
- Naumov, R. N.; Musina, E. I.; Kanunnikov, K. B.; Fesenko, T. I.; Krivolapov, D. B.; Litvinov, I. A.; Lönnecke, P.; Hey-Hawkins, E.; Karasik, A. A.; Sinyashin, O. G. Alternating Stereoselective Self-Assembly of SSSS/RRRR or RSSR Isomers of Tetrakisphosphines in the Row of 14-, 16-, 18- and 20-Membered Macrocycles. Dalton Trans. 2014, 43, 12784–12789. DOI: https://doi.org/10.1039/C4DT01619J.
- Musin, L. I.; Musina, E. I.; Kryvolapov, D. B.; Karasik, A. A.; Sinyashin, O. G. New 18-Membered Tetrakisphosphine Macrocycle and Its Derivatives. Phosphorus Sulfur Silicon Relat. Elem. 2016, 191, 1591–1592. DOI: https://doi.org/10.1080/10426507.2016.1216424.
- Kanunnikov, K. B.; Naumov, R. N.; Karasik, A. A.; Hey-Hawkins, E.-M.; Sinyashin, O. G. Stereoselective Synthesis of Novel 18- and 20-Membered P,N-Containing Macrocyclic Phosphine Ligands. Phosphorus Sulfur Silicon Relat. Elem. 2011, 186, 888–890. DOI: https://doi.org/10.1080/10426507.2010.511362.
- Musina, E. I.; Wittmann, T. I.; Shpagina, A. S.; Karasik, A. A.; Lönnecke, P.; Hey-Hawkins, E. Stereoselective Synthesis of the RPSPSPRP Isomer of 22-Membered P4N2 Macrocycles. Mendeleev Commun. 2020, 30, 697–699. DOI: https://doi.org/10.1016/j.mencom.2020.11.002.
- Naumov, R. N.; Karasik, A. A.; Kozlov, A. V.; Latypov, S. K.; Krivolapov, D. B.; Dobrynin, A. B.; Litvinov, I. A.; Kataeva, O. N.; Sinyashin, O. G.; Lönnecke, P.; Hey-Hawkins, E. Stereoselective Synthesis and Interconversions of 1,9-Diaza-3,7,11,15-Tetraphosphacyclohexadecanes. Phosphorus Sulfur Silicon Relat. Elem. 2008, 183, 456–459. DOI: https://doi.org/10.1080/10426500701761227.
- Karasik, A. A.; Sinyashin, O. G. Phosphorus Based Macrocyclic Ligands: Synthesis and Applications. In Phosphorus Compounds. Catalysis by Metal Complexes; Peruzzini, M., Gonsalvi, L., Eds.; Springer: Dordrecht, 2011; Vol. 37, pp. 375–444. DOI: https://doi.org/10.1007/978-90-481-3817-3_12.
- Musina, E. I.; Wittmann, T. I.; Karasik, A. A.; Sinyashin, O. G. Macrocyclic Tetraphosphine Corands and Their Complexes. Phosphorus Sulfur Silicon Relat. Elem. 2016, 191, 1444–1446. DOI: https://doi.org/10.1080/10426507.2016.1211653.
- Musina, E. I.; Wittmann, T. I.; Dobrynin, A. B.; Lönnecke, P.; Hey-Hawkins, E.; Karasik, A. A.; Sinyashin, O. G. Macrocyclic Tetrakis-Phosphines and Their Copper(I) Complexes. Pure Appl. Chem. 2017, 89, 331–339. DOI: https://doi.org/10.1515/pac-2016-1013.
- Naumov, R. N.; Kozlov, A. V.; Kanunnikov, K. B.; Gómez-Ruiz, S.; Hey-Hawkins, E.; Latypov, S. K.; Karasik, A. A.; Sinyashin, O. G. The First Example of Stereoselective Self-Assembly of a Cryptand Containing Four Asymmetric Intracyclic Phosphane Groups. Tetrahedron Lett. 2010, 51, 1034–1037. DOI: https://doi.org/10.1016/j.tetlet.2009.12.056.
- Omoruyi, U.; Page, S. J.; Apps, S.; White, A. J. P.; Long, N. J.; Miller, P. W. Synthesis and Characterisation of a Range of Fe, Co, Ru and Rh Triphos Complexes and Investigations into the Catalytic Hydrogenation of Levulinic Acid. J. Organomet. Chem. 2021, 935, id: 121650. DOI: https://doi.org/10.1016/j.jorganchem.2020.121650.
- Miller, P. W.; White, A. J. P. The Preparation of Multimetallic Complexes Using Sterically Bulky N-Centred Tripodal Dialkyl Phosphino Ligands. J. Organomet. Chem. 2010, 695, 1138–1145. DOI: https://doi.org/10.1016/j.jorganchem.2010.01.017.
- Westhues, N.; Klankermayer, J. Transfer Hydrogenation of Carbon Dioxide to Methanol Using a Molecular Ruthenium-Phosphine Catalyst. ChemCatChem 2019, 11, 3371–3375. DOI: https://doi.org/10.1002/cctc.201900932.
- Westhues, N.; Belleflamme, M.; Klankermayer, J. Base-Free Hydrogenation of Carbon Dioxide to Methyl Formate with a Molecular Ruthenium-Phosphine Catalyst. ChemCatChem 2019, 11, 5269–5274. DOI: https://doi.org/10.1002/cctc.201900627.
- Leopold, M.; Siebert, M.; Siegle, A. F.; Trapp, O. Reaction Network Analysis of the Ruthenium-Catalyzed Reduction of Carbon Dioxide to Dimethoxymethane. ChemCatChem 2021, 13, 2807–2814. DOI: https://doi.org/10.1002/cctc.202100437.
- Phanopoulos, A.; Nozaki, K. Branched-Selective Hydroformylation of Nonactivated Olefins Using an N-Triphos/Rh Catalyst. ACS Catal. 2018, 8, 5799–5809. DOI: https://doi.org/10.1021/acscatal.8b00566.
- Phanopoulos, A. The Coordination Chemistry and Catalytic Applications of Nitrogen-Centred Triphosphine Ligands. Ph.D. Dissertation, Imperial College London, London, UK, 2015.
- Phanopoulos, A.; Brown, N. J.; White, A. J. P.; Long, N. J.; Miller, P. W. Synthesis, Characterization, and Reactivity of Ruthenium Hydride Complexes of N-Centered Triphosphine Ligands. Inorg. Chem. 2014, 53, 3742–3752. DOI: https://doi.org/10.1021/ic500030k.
- Hanton, M. J.; Tin, S.; Boardman, B. J.; Miller, P. Ruthenium-Catalysed Hydrogenation of Esters Using Tripodal Phosphine Ligands. J. Mol. Catal. A Chem. 2011, 346, 70–78. DOI: https://doi.org/10.1016/j.molcata.2011.06.010.
- Scherl, P.; Kruckenberg, A.; Mader, S.; Wadepohl, H.; Gade, L. H. Ruthenium η4-Trimethylenemethane Complexes Containing Tripodal Phosphanomethylamine Ligands. Organometallics 2012, 31, 7024–7027. DOI: https://doi.org/10.1021/om300794h.
- Phanopoulos, A.; Miller, P. W.; Long, N. J. Beyond Triphos – New Hinges for a Classical Chelating Ligand. Coord. Chem. Rev. 2015, 299, 39–60. DOI: https://doi.org/10.1016/j.ccr.2015.04.001.
- Apps, S. Dinitrogen Activation of N-Triphos Transition Metal Complexes. Ph.D. Dissertation, Imperial College London, London, UK, 2019.
- Phanopoulos, A.; Long, N.; Miller, P. The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes. J. Vis. Exp. 2015, e52689. DOI: https://doi.org/10.3791/52689.
- Kellner, K.; Tzschach, A. Die Mannich-Reaktion als Synthesekonzept in der Phosphinchemie. Z Chem. 2010, 24, 365–375. DOI: https://doi.org/10.1002/zfch.19840241004.
- Fluck, E.; Meiser, P. Tris(Chlormethyl)Amin und Bis(Chlormethyl)Methylamin. Darstellung und Chemische Reaktionen. Chem. Ber. 1973, 106, 69–77. DOI: https://doi.org/10.1002/cber.19731060111.
- Walter, O.; Huttner, G.; Kern, R. Darstellung und Charakterisierung von N(CH2PPh2)3, N(CH2PPh2)3Mo(CO)3 und [HN(CH2PPh2)3Mo(CO)3]BF4. Z. Naturforsch. B 1996, 51, 922–928. DOI: https://doi.org/10.1515/znb-1996-0704.
- Janzen, A. F.; Dalziel, J. R.; Kay, S. N.; Galka, R. Reaction of Hexafluoroacetone and Hexafluoroisopropylidenimine with Thiols and Phosphines. J. Inorg. Nucl. Chem 1981, 43, 629–631. DOI: https://doi.org/10.1016/0022-1902(81)80526-X.
- Atton, J. G.; Kane-Maguire, L. A. P. Kinetics of Nucleophilic Attack on Coordinated Organic Moieties. Part 21. Factors Governing the Nucleophilicity of Phosphorus Nucleophiles towards [Fe(CO)3(1–5-η-C6H7)]+. J. Chem. Soc., Dalton Trans. 1982, 1491–1498. DOI: https://doi.org/10.1039/DT9820001491.
- Atton, J. G.; Kane-Maguire, L. A. P. Kinetics of Nucleophilic Attack on Coordinated Organic Moieties: XX. Novel Anchimeric Assistance in the Addition of Aryl Phosphines to [Fe(CO)3(1-5-η-C6H7)]. J. Organomet. Chem. 1982, 226, C43–C45. DOI: https://doi.org/10.1016/S0022-328X(00)87441-0.
- Kane-Maguire, L. A. P.; Manthey, M.; Atton, J. G.; John, G. R. Kinetics of Nucleophilic Attack on Coordinated Organic Moieties. Part 29. Mechanism of Addition of Tertiary Phosphines and Phosphites to the Tropylium Ring of [M(CO)3(η7-C7H7]+ (M = Cr, Mo, W) Cations. Inorg. Chim. Acta 1995, 240, 71–79. DOI: https://doi.org/10.1016/0020-1693(95)04518-X.
- Hoffmann, H. Umsetzungen von Phenylazid mit Yliden und Verwandten Verbindungen. Chem. Ber. 1962, 95, 2563–2566. DOI: https://doi.org/10.1002/cber.19620951032.
- Kischkel, H.; Röschenthaler, G.-V. Reaktionen von Phosphanen MenPH3-n (n = 0-3) mit Hexafluorisopropylidenimin. Z. Naturforsch. B 1984, 39, 356–358. DOI: https://doi.org/10.1515/znb-1984-0314.
- Moiseev, D. V.; James, B. R.; Hu, T. Q. α-Monodeuterated Benzyl Alcohols and Phosphobetaines from Reactions of Aromatic Aldehydes with a Water/D2O-Soluble Phosphine. Inorg. Chem. 2006, 45, 10338–10346. DOI: https://doi.org/10.1021/ic0613560.
- Voskuil, W.; Arens, J. F. Chemistry of Acetylenic Ethers. LXII: Tertiary Phosphines with an Acetylene-Phosphorus Bond. Recl. Trav. Chim. Pays-Bas 2010, 81, 993–1008. DOI: https://doi.org/10.1002/recl.19620811109.
- Adamek, J.; Zieleźny, P.; Erfurt, K. Synthesis of N-Protected 1-Aminoalkylphosphonium Salts from Amides, Carbamates, Lactams, or Imides. J. Org. Chem. 2021, 86, 5852–5862. DOI: https://doi.org/10.1021/acs.joc.1c00285.
- Kasukhin, L. F.; Brovarets, V. S.; Smolii, O. B.; Kurg, V. V.; Budnik, L. V.; Drach, B. S. N-Acylaminomethyl- and Substituted 1-Acylaminoethenylphosphonium Salts as Acetylcholinesterase Inhibitors. Zh. Obshch. Khim. 1991, 61, 2679–2684.
- Kozicka, D.; Zieleźny, P.; Erfurt, K.; Adamek, J. Amide-Type Substrates in the Synthesis of N-Protected 1-Aminomethylphosphonium Salts. Catalysts 2021, 11, 552. DOI: https://doi.org/10.3390/catal11050552.
- Frank, A. W. Synthesis and Properties of Tetrakis (Ureidomethyl)Phosphonium Salts. Phosphorus Sulfur Relat. Elem. 1978, 5, 19–25. DOI: https://doi.org/10.1080/03086647808069857.
- Frank, A. W.; Drake, G. L. Synthesis and Properties of Carbamate Derivatives of Tetrakis(Hydroxymethyl) Phosphonium Chloride. J. Org. Chem. 1977, 42, 4040–4045. DOI: https://doi.org/10.1021/jo00445a010.
- Petersen, H.; Reuther, W. α‐Ureidoalkylierung von Phosphor(III)‐Verbindungen. Justus Liebigs Ann. Chem. 1973, 766, 58–72. DOI: https://doi.org/10.1002/jlac.19727660108.
- Petersen, H.; Reuther, W. Production of Ureidomethylphosphonium Salts. U.S. Patent 3,658,804, Apr 25, 1972.
- Doherty, S.; Knight, J. G.; Scanlan, T. H.; Elsegood, M. R. J.; Clegg, W. Iminophosphines: Synthesis, Formation of 2,3-Dihydro-1H-Benzo[1,3]Azaphosphol-3-Ium Salts and N-(Pyridin-2-yl)-2-Diphenylphosphinoylaniline, Coordination Chemistry and Applications in Platinum Group Catalyzed Suzuki Coupling Reactions and Hydrosilylations. J. Organomet. Chem. 2002, 650, 231–248. DOI: https://doi.org/10.1016/S0022-328X(02)01203-2.
- Alonso, C.; Martín-Encinas, E.; Rubiales, G.; Palacios, F. Reliable Synthesis of Phosphino- and Phosphine Sulfide-1,2,3,4-Tetrahydroquinolines and Phosphine Sulfide Quinolines. Eur. J. Org. Chem. 2017, 2916–2924. DOI: https://doi.org/10.1002/ejoc.201700258.
- Milenković, M.; Warżajtis, B.; Rychlewska, U.; Radanović, D.; Anđelković, K.; Božić, T.; Vujčić, M.; Sladić, D. Synthesis, Spectral and Solid State Characterization of a New Bioactive Hydrazine Bridged Cyclic Diphosphonium Compound. Molecules 2012, 17, 2567–2578. DOI: https://doi.org/10.3390/molecules17032567.
- Adamek, J.; Mazurkiewicz, R.; Węgrzyk, A.; Erfurt, K. 1-Imidoalkylphosphonium Salts with Modulated Cα-P+Bond Strength: Synthesis and Application as New Active α-Imidoalkylating Agents. Beilstein J. Org. Chem. 2017, 13, 1446–1455. DOI: https://doi.org/10.3762/bjoc.13.142.
- Mazurkiewicz, R.; Adamek, J.; Październiok-Holewa, A.; Zielińska, K.; Simka, W.; Gajos, A.; Szymura, K. α-Amidoalkylating Agents from N-Acyl-α-Amino Acids: 1-(N-Acylamino)Alkyltriphenylphosphonium Salts. J. Org. Chem. 2012, 77, 1952–1960. DOI: https://doi.org/10.1021/jo202534u.
- Październiok-Holewa, A.; Walęcka-Kurczyk, A.; Musioł, S.; Stecko, S. Catalyst-Free Mannich-Type Reaction of 1-(N-Acylamino)Alkyltriphenylphosphonium Salts with Silyl Enolates. Tetrahedron 2019, 75, 732–742. DOI: https://doi.org/10.1016/j.tet.2018.12.042.
- Walęcka-Kurczyk, A.; Walczak, K.; Kuźnik, A.; Stecko, S.; Październiok-Holewa, A. The Synthesis of α-Aminophosphonates via Enantioselective Organocatalytic Reaction of 1-(N-Acylamino)Alkylphosphonium Salts with Dimethyl Phosphite. Molecules 2020, 25, id: 405. DOI: https://doi.org/10.3390/molecules25020405.
- Kuźnik, A.; Mazurkiewicz, R.; Grymel, M.; Zielińska, K.; Adamek, J.; Chmielewska, E.; Bochno, M.; Kubica, S. A New Method for the Synthesis of α-Aminoalkylidenebisphosphonates and Their Asymmetric Phosphonyl-Phosphinyl and Phosphonyl-Phosphinoyl Analogues. Beilstein J. Org. Chem. 2015, 11, 1418–1424. DOI: https://doi.org/10.3762/bjoc.11.153.
- Kuźnik, A.; Mazurkiewicz, R.; Zięba, M.; Erfurt, K. 1-(N-Acylamino)-1-Triphenylphosphoniumalkylphosphonates: General Synthesis and Prospects for Further Synthetic Applications. Tetrahedron Lett. 2018, 59, 3307–3310. DOI: https://doi.org/10.1016/j.tetlet.2018.07.040.
- Gorewoda, T.; Mazurkiewicz, R.; Simka, W.; Mlostoń, G.; Schroeder, G.; Kubicki, M.; Kuźnik, N. 3-Triphenylphosphonio-2,5-Piperazinediones as New Chiral Glycine Cation Equivalents. Tetrahedron Asymm. 2011, 22, 823–833. DOI: https://doi.org/10.1016/j.tetasy.2011.05.002.
- Mazurkiewicz, R.; Pierwocha, A. W.; Brachaczek, A.; Mitrus, I. Hydro-De-Phosphoniation of 4-Substituted-4-Triphenylphosphonio-5(4H)-Oxazolones with Alcohols. Phosphorus Sulfur Silicon Relat. Elem. 2000, 165, 43–52. DOI: https://doi.org/10.1080/10426500008076324.
- Mazurkiewicz, R.; Grymel, M. Reaction of N-Acyl-α-Triphenylphosphonio-α-Amino Acid Esters with Organic Bases: Mechanism of the Base-Catalyzed Nucleophilic Substitution of the Triphenylphosphonium Group. Monatsh. Chem. 2002, 133, 1197–1204. DOI: https://doi.org/10.1007/s007060200090.
- Mazurkiewicz, R.; Kuźnik, A.; Grymel, M.; Kuźnik, N. N-Acyl-α-Triphenylphosphonioglycinates in the Synthesis of α,β-Dehydro-α-Amino Acid Derivatives. Monatsh. Chem. 2004, 135, 807–815. DOI: https://doi.org/10.1007/s00706-003-0167-1.
- Mazurkiewicz, R.; Październiok-Holewa, A.; Orlińska, B.; Stecko, S. 1-(N-Acylamino)Alkyltriphenylphosphonium Salts as Synthetic Equivalents of N-Acylimines and New Effective α-Amidoalkylating Agents. Tetrahedron Lett. 2009, 50, 4606–4609. DOI: https://doi.org/10.1016/j.tetlet.2009.05.101.
- Październiok-Holewa, A.; Adamek, J.; Zielińska, K.; Piernikarczyk, K.; Mazurkiewicz, R. N. (1-Acylaminoalkyl) Amidinium Salts Derived from DBU or Related Bases as Reactive Intermediates in α-Amidoalkylation Reactions. ARKIVOC 2012, IV 314–329. DOI: https://doi.org/10.3998/ark.5550190.0013.423.
- Adamek, J.; Październiok-Holewa, A.; Zielińska, K.; Mazurkiewicz, R. Comparative Studies on the Amidoalkylating Properties of N-(1-Methoxyalkyl)Amides and 1-(N-Acylamino) Alkyltriphenylphosphonium Salts in the Michaelis-Arbuzov-like Reaction: A New One-Pot Transformation of N-(1-Methoxyalkyl)Amides into Phosphonic or Phosphinic Analogs of N-Acyl-α-Amino Acids. Phosphorus Sulfur Silicon Relat. Elem. 2013, 188, 967–980. DOI: https://doi.org/10.1080/10426507.2012.729237.
- Mazurkiewicz, R.; Grymel, M. N-Acyl-α-Triphenylphosphonioglycinates: A Novel Cationic Glycine Equivalent and Its Reactions with Heteroatom Nucleophiles. Monatsh. Chem. 1999, 130, 597–604. DOI: https://doi.org/10.1007/PL00010240.
- Październiok-Holewa, A.; Adamek, J.; Mazurkiewicz, R.; Zielińska, K. Amidoalkylating Properties of 1-(N-Acylamino)Alkyltriphenylphosphonium Salts. Phosphorus Sulfur Silicon Relat. Elem. 2013, 188, 205–212. DOI: https://doi.org/10.1080/10426507.2012.744014.
- Adamek, J.; Mazurkiewicz, R.; Październiok-Holewa, A.; Kuźnik, A.; Grymel, M.; Zielińska, K.; Simka, W. N-[1-(Benzotriazol-1-yl)Alkyl]Amides from N-Acyl-α-Amino Acids or N-Alkylamides. Tetrahedron 2014, 70, 5725–5729. DOI: https://doi.org/10.1016/j.tet.2014.06.068.
- Grymel, M.; Kuźnik, A.; Mazurkiewicz, R. N-Acyl-α-Triphenylphosphonio-α-Amino Acid Esters as Synthetic Equivalents of α-Amino Acid α-Cations. Phosphorus Sulfur Silicon Relat. Elem. 2015, 190, 429–439. DOI: https://doi.org/10.1080/10426507.2014.947412.
- Adamek, J.; Węgrzyk, A.; Kończewicz, J.; Walczak, K.; Erfurt, K. 1-(N-Acylamino)Alkyltriarylphosphonium Salts with Weakened Cα-P+ Bond Strength-Synthetic Applications. Molecules 2018, 23, id: 2453. DOI: https://doi.org/10.3390/molecules23102453.
- Adamek, J.; Węgrzyk, A.; Krawczyk, M.; Erfurt, K. Catalyst-Free Friedel-Crafts Reaction of 1-(N-Acylamino) Alkyltriarylphosphonium Salts with Electron-Rich Arenes. Tetrahedron 2018, 74, 2575–2583. DOI: https://doi.org/10.1016/j.tet.2018.03.053.
- Mazurkiewicz, R.; Grymel, M.; Kuźnik, A. Three New in situ Syntheses of N-Acyl-α-Triphenylphosphonioglycinates. Monatsh. Chem. 2004, 135, 799–806. DOI: https://doi.org/10.1007/s00706-003-0166-2.
- Adamek, J.; Mazurkiewicz, R.; Październiok-Holewa, A.; Grymel, M.; Kuźnik, A.; Zielińska, K. 1-(N-Acylamino)Alkyl Sulfones from N-Acyl-α-Amino Acids or N-Alkylamides. J. Org. Chem. 2014, 79, 2765–2770. DOI: https://doi.org/10.1021/jo500174a.
- Mazurkiewicz, R.; Październiok-Holewa, A.; Kononienko, A. A Novel Synthesis of 1-Aminoalkanephosphonic Acid Derivatives from 1-(N-Acylamino)-Alkyltriphenylphosphonium Salts. Phosphorus Sulfur Silicon Relat. Elem. 2010, 185, 1986–1992. DOI: https://doi.org/10.1080/10426500903436735.
- Zielińska, K.; Mazurkiewicz, R.; Szymańska, K.; Jarzębski, A.; Magiera, S.; Erfurt, K. Penicillin G Acylase-Mediated Kinetic Resolution of Racemic 1-(N-Acylamino)Alkylphosphonic and 1-(N-Acylamino)Alkylphosphinic Acids and Their Esters. J. Mol. Catal., B Enzym. 2016, 132, 31–40. DOI: https://doi.org/10.1016/j.molcatb.2016.05.011.
- Mazurkiewicz, R.; Kuźnik, A. A New Convenient Synthesis of N-Acyl-2-(Dimethoxyphosphoryl)Glycinates. Tetrahedron Lett. 2006, 47, 3439–3442. DOI: https://doi.org/10.1016/j.tetlet.2006.03.051.
- Mazurkiewicz, R.; Pierwocha, A. W. 4-Phosphoranylidene-5(4H)-Oxazolones—A Novel Synthesis and Properties. Monatsh. Chem. 1996, 127, 219–225. DOI: https://doi.org/10.1007/BF00807402.
- Mazurkiewicz, R.; Pierwocha, A. W. 4-Phosphoranylidene-5(4H)-Oxazolones II. Reactions with Alkylating Agents. Monatsh. Chem. 1997, 128, 893–900. DOI: https://doi.org/10.1007/BF00807098.
- Mazurkiewicz, R.; Grymel, M. Reaction of 4-Phosphoranylidene-5(4H)-Oxazolones with Acylating Agents. Polish J. Chem. 1998, 72, 537–547.
- Mazurkiewicz, R.; Październiok-Holewa, A.; Grymel, M. Synthesis and Decarboxylation of N-Acyl-α-Triphenylphosphonio-α-Amino Acids: A New Synthesis of α-(N-Acylamino) Alkyltriphenylphosphonium Salts. Tetrahedron Lett. 2008, 49, 1801–1803. DOI: https://doi.org/10.1016/j.tetlet.2008.01.051.
- Mazurkiewicz, R.; Październiok-Holewa, A.; Grymel, M. N-Acyl-α-Triphenylphosphonio-α-Amino Acids: Synthesis and Decarboxylation to α-(N-Acylamino)Alkyltriphenylphosphonium Salts. Phosphorus Sulfur Silicon Relat. Elem. 2009, 184, 1017–1027. DOI: https://doi.org/10.1080/10426500902720204.
- Adamek, J.; Mrowiec-Białoń, J.; Październiok-Holewa, A.; Mazurkiewicz, R. Thermogravimetrical Investigations of the Dealkoxycarbonylation of N-Acyl-α-Triphenylphosphonioglycinates. Thermochim. Acta 2011, 512, 22–27. DOI: https://doi.org/10.1016/j.tca.2010.08.017.
- Knoll, F.; Krumm, U. Des Dimethyl-Chlormethyl-Amins mit Lewis-Säuren und -Basen. Chem. Ber. 1971, 104, 31–39. DOI: https://doi.org/10.1002/cber.19711040106.
- Böhme, H.; Haake, M. Über α-Halogenierte Amine, XLI. Zur Reaktivität von Methyleniminium-Salzen Gegenüber Schwach Basischen Aminen und Phosphinen. Chem. Ber. 1972, 105, 2233–2236. DOI: https://doi.org/10.1002/cber.19721050716.
- Opitz, G.; Griesinger, A.; Schubert, H. W.; Enamine, XII. Umsetzung von Tertiären Enamin-Salzen mit Nucleophilen Verbindungen. Justus Liebigs Ann. Chem. 1963, 665, 91–101. DOI: https://doi.org/10.1002/jlac.19636650112.
- Böhme, H.; Haake, M. Über α-Halogenierte Amine. XXII. N-[α-Chlor-4-Dimethylamino-Benzyl]-Morpholin, Ein Farbiges α-Halogeniertes Amin. Chem. Ber. 1967, 100, 3609–3613. DOI: https://doi.org/10.1002/cber.19671001116.
- Drach, B. S.; Sviridov, E. P.; Kirsanov, A. V. Interaction of N-Chloromethylamides with Triphenylphosphines. Zh. Obshch. Khim. 1972, 42, 953–954.
- Moiseev, D. V.; James, B. R.; Gushchin, A. V. Interaction of PH3 with Acetaldehyde in Aqueous Media and Chemistry of [HO(Me)CH]4PCl. Russ. J. Gen. Chem. 2013, 83, 252–259. DOI: https://doi.org/10.1134/S1070363213020047.
- Canac, Y.; Conejero, S.; Soleilhavoup, M.; Donnadieu, B.; Bertrand, G. Synthesis of Transient and Stable C-Amino Phosphorus Ylides and Their Fragmentation into Transient and Stable Carbenes. J. Am. Chem. Soc. 2006, 128, 459–464. DOI: https://doi.org/10.1021/ja055863c.
- Allefeld, N.; Neumann, B.; Stammler, H.-G.; Röschenthaler, G.-V.; Ignat'ev, N.; Hoge, B. Synthesis and Reactivity of New Functionalized Perfluoroalkylfluorophosphates. Chemistry 2014, 20, 7736–7745. DOI: https://doi.org/10.1002/chem.201402421.
- Hellmann, H.; Schumacher, O. Quartäre Phosphoniumsalze aus Tertiären Phosphinen und Quartären Ammoniumsalzen. Justus Liebigs Ann. Chem. 1961, 640, 79–84. DOI: https://doi.org/10.1002/jlac.19616400110.
- Ernest, I.; Gosteli, J.; Greengrass, C. W.; Holick, W.; Pfaendler, H. R.; Woodward, R. B. The Penems, a New Class of β-Lactam Antibiotics: 6-Acylaminopenem-3-Carboxylic Acids. J. Am. Chem. Soc. 1978, 100, 8214–8222. DOI: https://doi.org/10.1021/ja00494a032.
- Lang, M.; Prasad, K.; Holick, W.; Gosteli, J.; Ernest, I.; Woodward, R. B. The Penems, a New Class of β-Lactam Antibiotics. 2. Total Synthesis of Racemic 6-Unsubstituted Representatives. J. Am. Chem. Soc. 1979, 101, 6296–6301. DOI: https://doi.org/10.1021/ja00515a024.
- Ernest, I.; Gosteli, J.; Woodward, R. B. The Penems, a New Class of β-Lactam Antibiotics. 3. Synthesis of Optically Active 2-Methyl-(5R)-Penem-3-Carboxylic Acid. J. Am. Chem. Soc. 1979, 101, 6301–6305. DOI: https://doi.org/10.1021/ja00515a025.
- Pfaendler, H. R.; Gosteli, J.; Woodward, R. B. The Penems, a New Class of β-Lactam Antibiotics. 4. Syntheses of Racemic and Enantiomeric Penem Carboxylic Acids. J. Am. Chem. Soc. 1979, 101, 6306–6310. DOI: https://doi.org/10.1021/ja00515a026.
- Ponsford, R. J.; Roberts, P. M.; Southgate, R. Intramolecular Wittig Reactions with Thioesters: The Synthesis of 7-Oxo-3-Phenylthio-1-Azabicyclo[3.2.0]Hept-2-Ene-2-Carboxylates. J. Chem. Soc., Chem. Commun. 1979, 847–848. DOI: https://doi.org/10.1039/c39790000847.
- Grodner, J.; Chmielewski, M. Synthesis of (6R) 4-t-Butoxycarbonyl-7-Hydroxymethyl-1-Oxa-3-Cephem from D-Arabinal. Tetrahedron 1995, 51, 829–836. DOI: https://doi.org/10.1016/0040-4020(94)00954-S.
- Kober, R.; Steglich, W. Untersuchungen zur Reaktion von Acylaminobrommalonestern und Acylaminobromessigestern mit Trialkylphosphiten – Eine Einfache Synthese von 2‐Amino‐2‐(Diethoxyphosphoryl)Essigsäure‐Ethylester. Liebigs Ann. Chem. 1983, 599–609. DOI: https://doi.org/10.1002/jlac.198319830409.
- Shokol, V. A.; Kozhushko, B. N.; Gumenyuk, A. V. Trialkyl- and Aryldialkyl(Isocyanatomethyl)Ammonium Chlorides. Zh. Obshch. Khim. 1977, 47, 1110–1118.
- Smolii, O. B.; Brovarets, V. S.; Pirozhenko, V. V.; Drach, B. S. Cyclocondensation of N-Substituted Imidoyl Chlorides Containing a Phosphonium Group. Zh. Obshch. Khim. 1988, 58, 2465–2471.
- Smolii, O. B.; Brovarets, V. S.; Drach, B. S. Substituted Methylphosphonium Salts with an Imidoyl Chloride Group. Zh. Obshch. Khim. 1986, 56, 2802–2803.
- Drach, B. S.; Dolgushina, I. Y.; Sinitsa, A. D. Application of ω-Chloro-ω-Acylaminoacetophenones for Synthesis of Phosphorylated Oxazoles. Zh. Obshch. Khim. 1975, 45, 1251–1255.
- Brovarets, V. S.; Lobanov, O. P.; Vinogradova, T. K.; Drach, B. S. Preparation and Properties of 2-Chloro-1-Acylaminovinyltriphenylphosphonium Chlorides. Zh. Obshch. Khim. 1984, 54, 288–301.
- Drach, B. S.; Sviridov, E. P.; Kirsanov, A. V. Reaction of N-1,2,2,2-Tetrachloroethylamides of Acids with Diphenylphosphinous Acid Ethyl Ester and Triphenylphosphine. Zh. Obshch. Khim. 1975, 45, 12–16.
- Drach, B. S.; Brovarets, V. S.; Smolii, O. B. Acylamino-Substituted Vinylphosphonium Salts in Syntheses of Derivatives of Nitrogen Heterocycles. Russ. J. Gen. Chem. 2002, 72, 1661–1687. DOI: https://doi.org/10.1023/A:1023320608504.
- Kozhushko, B. N.; Gumenyuk, A. V.; Paliichuk, Y. A.; Shokol, V. A. Trialkyl- and Triaryl(Isocyanatomethyl) Chlorophosphoranes. Zh. Obshch. Khim. 1977, 47, 333–339.
- Shokol, V. A.; Doroshenko, V. V.; Dergach, G. I. Phosphorus Isocyanates. Zh. Obshch. Khim. 1969, 39, 214–215.
- Acharya, S. Synthesis of P-Isopropylacetonate-N-Methyl-1,3,5-Triaza-7-Phosphaadamantane. Chem. Res. J. 2017, 2, 98–103.