References
- Le Noble WJ. Organic high pressure chemistry. Amsterdam: Elsevier; 1988.
- Isaacs NS. Liquid phase high pressure chemistry. Chichester: John Wiley; 1981.
- van Eldik R, Klärner F-G. High pressure chemistry: synthetic, mechanistic, and supercritical applications. Weinheim: Wiley; 2002.
- Drljaca A, Hubbard CD, van Eldik R, et al. Activation and reaction volumes in solution. 3. Chem Rev. 1998;98:2167–2290. doi: 10.1021/cr970461b
- Klarner F-G, Krawczyk B, Ruster V, et al. Evidence for Pericyclic and stepwise processes in the cyclodimerization of chloroprene and 1,3-butadiene from pressure dependence and stereochemistry. experimental and theoretical volumes of activation and reaction. J Am Chem Soc. 1994;116:7646–7657. doi: 10.1021/ja00096a023
- Matsumoto K, Hamana H, Iida H. Compendium of cycloaddition reactions under high pressure. Helv Chim Acta. 2005;88:2033–2234. doi: 10.1002/hlca.200590156
- Kiselev VD, Konovalov AI, Asano T, et al. Solvent effect on the volume of activation and volume of the Diels–Alder reaction. J Phys Org Chem. 2001;14:636–643. doi: 10.1002/poc.398
- Iskhakova GG, Kiselev VD, Kashaeva EA, et al. Diels-Alder reaction between naphthalene and N-phenylmaleimide under ambient and high pressure conditions. Arkivoc. 2004;2004:70–79.
- Kotsuki H, Nishizawa H, Kitagawa S, et al. High pressure organic chemistry. III. Diels-Alder reaction of thiophene with maleic anhydride. Bull Chem Soc Jpn. 1979;52:544–548. doi: 10.1246/bcsj.52.544
- McCluskey A, Keane MA, Walkom CC, et al. The first two Cantharidin analogues displaying PP1 selectivity. Bioorg Med Chem Lett. 2002;12:391–393. doi: 10.1016/S0960-894X(01)00777-6
- Jenner G. The pressure effect on strained transition states. Correlation between strain and volume of activation: mechanistic and synthetic involvements. J Chem Soc, Faraday Trans. 1985;81:2437–2460. doi: 10.1039/f19858102437
- Tamura K, Imoto T. Solvent effects under high pressure. II. determination and applications to kinetic studies of the ET-value at high pressures. Bull Chem Soc Jpn. 1975;48:369–374. doi: 10.1246/bcsj.48.369
- Kiselev VD, Kornilov DA, Konovalov AI. Changes in permittivity and density of molecular liquids under high pressure. J Phys Chem B. 2014;118:3702–3709. doi: 10.1021/jp501344t
- Kiselev VD. High-pressure influence on the rate of Diels-Alder cycloaddition reactions of maleic anhydride with some dienes. Int J Chem Kinet. 2013;45:613–622. doi: 10.1002/kin.20800
- Kiselev VD, Kashaeva EA, Shihab MS, et al. Diffusion control of the Diels—Alder reaction rate at elevated pressures. Russ Chem Bull. 2004;53:45–50. doi: 10.1023/B:RUCB.0000024827.64458.0f
- Konovalov AI, Kiselev VD. Diels-Alder reaction. Effect of internal and external factors on the reactivity of diene-dienophile systems. Russ Chem Bull. 2003;52:293–311. doi: 10.1023/A:1023486127587
- Sauer J. Diels-Alder-Reaktionen: Zum Reaktionsmechanismus. Angew Chem. 1967;79:76–94. doi: 10.1002/ange.19670790203
- Kiselev VD, Kashaeva EA, Konovalov AI. Pressure effect on the rate and equilibrium constants of the Diels-Alder reaction 9-chloroanthracene with tetracyanoethylene. Tetrahedron. 1999;55:1153–1162. doi: 10.1016/S0040-4020(98)01093-X
- Kornilov DA, Kiselev VD, Konovalov AI. Determination of the reaction acceleration effect at an elevated hydrostatic pressure. Russ Chem Bull. 2017;66:564–566. doi: 10.1007/s11172-017-1772-1
- Kiselev VD, Bolotov AV, Satonin AP, et al. Compressibility of liquids. Rule of noncrossing V−P curvatures. J Phys Chem B. 2008;112:6674–6682. doi: 10.1021/jp800513d
- Le Neindre B, Vodar B. Experimental thermodynamics, volume II: experimental thermodynamics of non-reacting fluids. London: Elsevier; 1975.
- Lide DR, Frederikse HPR. Handbook of chemistry and physics. 75th ed. Boca Raton: CRC Press; 1994–1995.
- Bridgman PW. The compression of sixty-one solid substances to 25,000 kg/cm2, determined by a new rapid method. Proc Am Acad Arts Sci. 1945;76:9–24. doi: 10.2307/20023492
- Dai Y, Wang K, Li X, et al. High-pressure-induced planarity of the molecular arrangement in maleic anhydride. J Phys Chem C. 2016;120:18503–18509. doi: 10.1021/acs.jpcc.6b06351
- Kiselev VD. Why can the activation volume of the cycloadduct decomposition in isopolar retro-Diels-Alder reactions be negative? Int J Chem Kinet. 2010;42:117–125. doi: 10.1002/kin.20462
- Yoshimura Y, Osugi J, Nakahara M. Volumetric study on the 1,3-Dipolar cycloaddition reaction of Diazodiphenylmethane with several Olefins. Bull Chem Soc Jpn. 1983;56:680–683. doi: 10.1246/bcsj.56.680
- Firestone RA, Smith GM. The roles of changes in bonding vs. packing fraction in the pressure-induced acceleration of the Diels-Alder reaction. Chem Ber. 1989;122:1089–1094. doi: 10.1002/cber.19891220614
- Swiss KA, Firestone RA. Phantom activation volumes1. J Phys Chem A. 2000;104:3057–3063. doi: 10.1021/jp9935900
- Bekoe DA, Trueblood KN. The crystal structure of tetracyanoethylene. Z Kristallogr New Cryst Struct. 1960;113:1–22.
- Drück U, Guth H. A new refinement of monoclinic tetracyanoethylene (TCNE) from X-ray and neutron data. Z Kristallogr New Cryst Struct. 1982;161:103–110. doi: 10.1524/zkri.1982.161.1-2.103
- Chaplot SL, Mierzejewski A, Pawley GS. The monoclinic structure of tetracyanoethylene (TCNE), C6N4, at 5,150 and 295 K; powder diffraction analysis. Acta Crystallogr, Sect C. 1984;40:663–666. doi: 10.1107/S0108270184005254
- Chaplot SL, Chakravarthy R, David WIF, et al. The phonon density of states and high-resolution crystal structure of monoclinic tetracyanoethylene. J Phys: Condens Matter. 1991;3:9271–9277.
- Marsh RE, Ubell E, Wilcox HE. The crystal structure of maleic anhydride. Acta Crystallogr. 1962;15:35–41. doi: 10.1107/S0365110X62000080
- Kajfez T, Kamenar B, Pilizota V, et al. Crystal and molecular structures of N-Phenylmaleimide and N-Phenyl-2,3-dimethylmaleimide. Croat Chem Acta. 2003;76:343–346.
- Mason R. The crystallography of anthracene at 95°K and 290°K. Acta Crystallogr. 1964;17:547–555. doi: 10.1107/S0365110X64001281
- Mathieson A, Robertson JM, Sinclair VC. The crystal and molecular structure of anthracene. I. X-ray measurements. Acta Crystallogr. 1950;3:245–250. doi: 10.1107/S0365110X50000641
- Ahmed FR, Cruickshank DWJ. A refinement of the crystal and molecular structures of naphthalene and anthracene. Acta Crystallogr. 1952;5:852–853. doi: 10.1107/S0365110X52002379
- Cruickshank DWJ. A detailed refinement of the crystal and molecular structure of anthracene. Acta Crystallogr. 1956;9:915–923. doi: 10.1107/S0365110X56002588
- Ponomarev VI, Shilov GV. The crystal structure of anthracene in the range 300-100 K. Sov Phys Crystallogr. 1983;28:397–399.
- Brock CP, Dunitz JD. Temperature dependence of thermal motion in crystalline anthracene. Acta Crystallogr Sect B. 1990;46:795–806. doi: 10.1107/S0108768190008382
- Drenth W, Wiebenga EH. Structure of α,ω-diphenylpolyenes.: I. crystal data of 1,4-diphenyl-1,3-butadiene, 1,6-diphenyl-1,3,5-hexatriene and 1,8-diphenyl-1,3,5,7-octatetraene. Rec Trav Chim Pays-Bas. 1953;72:39–43. doi: 10.1002/recl.19530720104
- Karle IL, Fratini AV. The crystal structure of the anthracene–tetracyanoethylene adduct and complex 8C20H10N4.2CH2Cl2.C6N4. Acta Crystallogr, Sect B. 1970;26:596–606. doi: 10.1107/S0567740870002844
- Bulgarovskii IV, Zvonkova ZV, Il’ina IG. Molecular and crystal structure of the adduct of anthracene with maleic anhydride. J Struct Chem. 1980;20:755–759. doi: 10.1007/BF00746775
- de Delgado GD, Ramirez BV, Velasquez W, et al. A new polymorph of 9,10-dihydroanthracene-9,10-α,β-succinic acid anhydride. Acta Crystallogr Sect E. 2002;58:o501–o503. doi: 10.1107/S1600536802005767
- Murty BVR. Refinement of the structure of anthraquinone*. Z Kristallogr New Cryst Struct. 1960;113:445–465. doi: 10.1524/zkri.1960.113.1-6.445
- Lonsdale K, Milledge J, El Sayed K. The crystal structure (at five temperatures) and anisotropic thermal expansion of anthraquinone. Acta Crystallogr. 1966;20:1–13. doi: 10.1107/S0365110X6600001X
- Prakash A. Refinement of the crystal structure of anthraquinone. Acta Crystallogr. 1967;22:439–440. doi: 10.1107/S0365110X67000878
- Lenstra ATH, van Loock JFJ. A note on the crystal structure of 9,10- anthraquinone. Bull Soc Chim Belg. 1984;93:1053–1055. doi: 10.1002/bscb.19840931204
- Guha BC. X-ray analysis of the structure of anthraquinone. Philos Mag. 1938;26:213–223. doi: 10.1080/14786443808562117
- Herbstein FH, Kapon M, Reisner GM. Molecular compounds and complexes. XVI. 9,10-dihydroanthracene (I) (C14H12) (a redetermination) and 9,10-dihydroanthracene:bis(1,3,5-trinitrobenzene) (II) (C14H12.C6H3N3O6). Acta Crystallogr Sect B. 1986;42:181–187. doi: 10.1107/S0108768186098385
- Reboul JP, Oddon Y, Caranoni C, et al. Structure du dihydro-9,10 anthracène. Support tricyclique de médicaments psychotropes. Acta Crystallogr Sect C. 1987;43:537–539. doi: 10.1107/S010827018709512X
- Ruelle P, Farina-Cuendet A, Kesselring UW. Changes of molar volume from solid to liquid and solution: the particular case of C60. J Am Chem Soc. 1996;118:1777–1784. doi: 10.1021/ja953467w
- Smith AL, Walter E, Korobov MV, et al. Some enthalpies of solution of C60 and C70. Thermodynamics of the temperature dependence of fullerene solubility. J Phys Chem. 1996;100:6775–6780. doi: 10.1021/jp952873z