Synthesis and mesomorphic properties of iron(II)-containing dendrimeric complexes derivative of 3,4-n-dodecyloxybenzoyl poly(propylene imine)

References

• Lee CC, MacKay JA, Fréchet JMJ, et al. Designing dendrimers for biological applications. Nat Biotechnol. 2005;23:1517–1526. doi:10.1038/nbt1171.
   PubMed Web of Science ®Google Scholar
• Frechet JMJ. Functional polymers and dendrimers: reactivity, molecular architecture, and interfacial energy. Science. 1994;263:1710–1715. doi:10.1126/science.8134834.
   PubMed Web of Science ®Google Scholar
• Tomalia DA. Starburst/cascade dendrimers: fundamental building blocks for a new nanoscopic chemistry set. Aldrichim Acta. 1993;26:91–101.
   Google Scholar
• Astruc D, Boisselier E, Ornelas C. Dendrimers designed for functions: from physical, photophysical, and supramolecular properties to applications in sensing, catalysis, molecular electronics, photonics, and nanomedicine. Chem Rev. 2010;110:1857–1959. doi:10.1021/cr900327d.
   PubMed Web of Science ®Google Scholar
• Mark SS, Sandhyarani N, Zhu CC, et al. Dendrimer-functionalized self-assembled monolayers as a surface plasmon resonance sensor surface. Langmuir. 2004;20:6808–6817. doi:10.1021/la0495276.
   PubMed Web of Science ®Google Scholar
• Twyman LJ, King ASH, Martin IK. Catalysis inside dendrimers. Chem Soc Rev. 2002;31:69–82. doi:10.1039/B107812G.
   PubMed Web of Science ®Google Scholar
• Zeng F, Zimmerman SC. Dendrimers in supramolecular chemistry: from molecular recognition to self-assembly. Chem Rev. 1997;97(5):1681–1712. doi:10.1021/cr9603892.
   PubMed Web of Science ®Google Scholar
• Cuadrado I, Morán M, Casado CM, et al. Organometallic dendrimers with transition metals. Coord Chem Rev. 1999;193–195:395–445. doi:10.1016/S0010-8545(99)00036-3.
   Web of Science ®Google Scholar
• Donnio B, Buathong S, Bury I, et al. Liquid crystalline dendrimers. Chem Soc Rev. 2007;36:1495–1513. doi:10.1039/B605531C.
   PubMed Web of Science ®Google Scholar
• Donnio B. Liquid-crystalline metallodendrimers. Inorgan Chim Acta. 2014;409:53–67. doi:10.1016/j.ica.2013.07.045.
   Web of Science ®Google Scholar
• Cameron JH, Facher A, Lattermann G, et al. Poly(propyleneimine) dendromesogens with hexagonal columnar mesophase. Adv Mater. 1997;9:398–403. doi:10.1002/adma.19970090507.
   Web of Science ®Google Scholar
• Usol’tseva N, Bykova V, Smirnova A, et al. Induction of mesomorphic properties in poly(propylene imine) dendrimers and their model compounds. Mol Cryst Liq Cryst. 2004;409:29–42. doi:10.1080/15421400490435495.
   Web of Science ®Google Scholar
• Barberá J, Donnio B, Gehringer L, et al. Self-organization of nanostructured functional dendrimers. J Mater Chem. 2005;15:4093–4105. doi:10.1039/B502464A.
   Web of Science ®Google Scholar
• Donnio B, Barberá J, Giménez R, et al. Controlled molecular conformation and morphology in poly(amidoamine) (PAMAM) and poly(propyleneimine) (DAB) dendrimers. Macromolecules. 2002;35:370–381. doi:10.1021/ma010881.
   Web of Science ®Google Scholar
• Stebani U, Lattermann G, Wittenberg M. Metallomesogene mit verzweigten dendrimeren Aminoliganden. Angew Chem. 1996;108(16):1941–1943. doi:10.1002/ange.19961081614.
   Google Scholar
• Barberá J, Marcos M, Serrano JL. Dendromesogens: liquid crystal organizations versus starburst structures. Chem Eur J. 1999;5:1834–1840. doi:10.1002/(SICI)1521-3765(19990604)5:6<1834::AID-CHEM1834>3.0.CO;2-A.
   Web of Science ®Google Scholar
• Domracheva N, Mirea A, Schwoerer M, et al. EPR Characterisation of CuII complexes of poly(propylene imine) dendromesogens: using the orienting effect of a magnetic field. Chem Phys Chem. 2005;6:110–119. doi:10.1002/cphc.200400328.
   Web of Science ®Google Scholar
• Domracheva N, Mirea A, Schwoerer M, et al. Magnetic properties of poly(propylene imine)-copper dendromesogenic complexes: an EPR study. Chem Phys Chem. 2006;7(12):2567–2577. doi:10.1002/cphc.200600360.
   Web of Science ®Google Scholar
• Bosman AW, Schenning APH, Janssen RAJ, et al. Well-defined metallodendrimers by site-specific complexation. Chem Ber Recueil. 1997;130:725–728. doi:10.1002/cber.19971300608.
   Google Scholar
• Barefield EK, Carrier AM, Vanderveer DG. X-ray structure of Mer-Trichloro[N-(3-aminopropyl)-1,3-diaminopropane]cobalt(III). Inorg Chim Acta. 1980;42:271–275. doi:10.1016/S0020-1693(00)88925-2.
   Web of Science ®Google Scholar
• House DA, Robinson WT. Chromium(III) complexes with 1,5,9-triazanonane (3,3-tri)-CrX3(3,3-tri)n+ and CrCl(diamine)(3,3-tri)2+. Inorg Chim Acta. 1988;141:211–220. doi:10.1016/S0020-1693(00)83912-2.
   Web of Science ®Google Scholar
• Vassilev K, Turmanova S, Dimitrova M, et al. Poly(propylene imine) dendrimer complexes as catalysts for oxidation of alkenes. Eur Polym J. 2009;45:2269–2278. doi:10.1016/j.eurpolymj.2009.05.012.
   Web of Science ®Google Scholar
• Carvalho NMF, Horn A Jr, Bortoluzzi AJ, et al. Synthesis and characterization of three mononuclear Fe(III) complexes containing bipodal and tripodal ligands: X-ray molecular structure of the dichloro[N-propanamide-N, N-bis-(2-pyridylmethyl)amine]iron(III) perchlorate. Inorg Chim Acta. 2006;359:90–98. doi:10.1016/j.ica.2005.07.010.
   Web of Science ®Google Scholar
• Nakajima R, Tsuruta M, Higuchi M, et al. Fine control of the release and encapsulation of Fe ions in dendrimers through ferritin-like redox switching. J Am Chem Soc. 2004;126:1630–1631. doi:10.1021/ja037480p.
   PubMed Web of Science ®Google Scholar
• Wang P-W, Liu Y-J, Devadoss C, et al. Electroluminescent diodes from a single component emitting layer of dendritic macromolecules. Adv Mater. 1996;8(3):237–241. doi:10.1002/adma.19960080311.
   Web of Science ®Google Scholar
• Sooklal K, Hanus LH, Ploehn HJ, et al. A blue-emitting Cds/dendrimer nanocomposite. Adv Mater. 1998;10:1083–1087. doi:10.1002/(SICI)1521-4095(199810)10:14<1083::AID-ADMA1083>3.0.CO;2-B.
   Web of Science ®Google Scholar
• Gruzdev MS. The influence of molecular structure of dendrimer complexes and nanocomposites – derivatives of poly(propylene imine) on their mesomorphic properties [ Candidate Sci. (Chem.) Dissertation]. Ivanovo (Russia): Ivanovo State University; 2006.
   Google Scholar
• Pretch E. Evaluation of structure of organic compounds. Moscow: Mir; 2006.
   Google Scholar
• Romanova V, Begishev V, Karmanov V, et al. Fourier transform Raman and Fourier transform infrared spectra of cross-linked polyurethaneurea films synthesized from solutions. J Raman Spectrosc. 2002;33:769–777. doi:10.1002/jrs.914.
   Web of Science ®Google Scholar
• Malval J-P, Lapouyade R. Derivatization of 4-(dimethylamino)benzamide to dual fluorescent ionophores: divergent spectroscopic effects dependent on N or O amide chelation. Helv Chim Acta. 2001;84(9):2439–2451. doi:10.1002/1522-2675(20010919)84:9<2439::AID-HLCA2439>3.0.CO;2-S.
   Web of Science ®Google Scholar
• Hearle JWS. Polymers and their properties. Volume 1: fundamentals of structure and mechanics. New York (NY): Wiley; 1982.
   Google Scholar
• Lindenmeyer PH. A molecular theory of polymer chain folding. J Pol Sci Part C. 1967;20:145–158. doi:10.1002/polc.5070200113.
   Google Scholar