Determination of the Apparent Molar Refraction and Partial Molar Volume at Infinite Dilution of Thiophene-, Pyrrole- and Furan-2-Carboxaldehyde Phenylhydrazone Derivatives in Acetonitrile at 293.15 K
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Published:2006-12-07
Issue:1
Volume:36
Page:1-11
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ISSN:0095-9782
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Container-title:Journal of Solution Chemistry
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language:en
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Short-container-title:J Solution Chem
Author:
Alvarado Ysaías J.,Caldera-Luzardo José,Ferrer-Amado Gladys,Mancilla-Labarca Victoria,Michelena Elba
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Molecular Biology,Biochemistry,Biophysics
Reference22 articles.
1. a) Lewis, M., Barrer, C., Hathaway, B., Glaser, R.: 4-Methoxybenzaldehyde pentafluorophenyl-methylindenehydarzone. Acta Cryst. C55, 975–978 (1999); b) Serbutoviez, C., Bosshard, C., Knöpfle, G., Wyss, P., Prêtre, P., Gunter, P., Schenk, K., Solari, E., Chapuis, G.: Hydrazone derivatives, an efficient class of crystalline materials for nonlinear optics. Chem. Mater. 7, 1198–1206 (1995); c) Follonier, S., Bosshard, C., Meier, U., Knöpfle, G., Serbutoviez, C., Pan, F., Günter, P.: New nonlinear organic crystal: 4-dimethyl-aminobenzaldehyde-4-nitrophenyl-hydrazone. J. Opt. Soc. Am. 14, 593–600 (1997); d) Wong, M., Gramlich, V., Pan, F., Bosshard, C., Günter, P.: 5-Mehylthiophene-2-carboxaldehyde-water(1/1). Acta Cryst. C53, 757–759 (1997). 2. a) Galey, J., Bombard, S., Chopard, C., Girerd, J., Lederer, F., Thang, D., Nam, N., Mansuy, D., Chottard, J.: Hexanal phenylhydrazone is a mechanism-based inactivator of soybean lipoxygenase 1. Biochem. 27, 1058–1066 (1988); b) Mahy, J., Gaspard, S., Mansuy, D.: Phenylhydrazone as new good substrates for the dioxygenase and peroxidase reactions of prostaglandin synthase: formation of iron(III)-σ-phenyl complexes. Biochem. 32, 4104–4021 (1993); c) Mague, J., Vang, S., Berge, D., Wacholtz, W.: Isomerism/tautomerism in hydrazones derived from thiophenaldehydes and 2-hydrazoquinoline. Acta Cryst, C53, 973–979 (1997); d) Ding, W., Jiang, X.: Correlation analysis of UV spectral data of some phenylhydrazones and semicarbazones by the dual-parameter equation. Observation of three types of behaviors of the λmax values induced by the polar effects of subtituents. J. Phys. Org. Chem. 11, 809–818 (1998); e) Pan, F., Wong, M., Bösch, M., Bosshard, C., Meier, U., Günter, P.: A highly efficient organic second-order nonlinear optical crystal based on donor-acceptor substituted 4-nitrophenylhydarzone. Appl. Phys. Lett. 71, 2064–2066 (1997); f) Thami, T., Bassoul, P., Petit, M., Simon, J., Fort, A., Barzoukas, M., Villaeys, A.: Highly polarizable metallic complexes for nonlinear optics. Cobaltous complexes of unsymmetrical hydrazone imine glyoxal derivatives. J. Am. Chem. Soc. 114, 915–921 (1992). 3. a) Moscovici, R., Ferraz, J., Neves, E., Tognoli, J., Seoud, M. do Amaral, L.: Mechanism and catalysis for phenylhydrazone formation from aromatic heterocyclic aldehydes. J. Org. Chem. 41, 4093–4096 (1976); b) Amaral, L.: Mechanism and catalysis for furfural phenylhydrazone formation. J. Org. Chem. 37, 1433–1436 (1972); c) Westerman, P., Botto, R., Boberts J.: Substituent and medium effects on nitrogen-15 shielding of compounds with >C=N bonds (imines, oximes, and phenylhydrazones). J. Org. Chem. 43, 2590–2596 (1978); d) Pacansky, J., McLean, A.D., Miller, M.D.: Theoretical calculations and experimental studies on the electronic structures of hydrazones and hydrazone radical cations: formaldehyde hydrazone and benzaldehyde diphenylhydrazones. J. Phys. Chem. 94, 90–98 (1990). 4. a) Soscún, H., Alvarado, Y., Hernández, J., Hernández, P., Atencio, R., Hinchliffe, A.: Experimental and theoretical determination of the dipole polarizability of dibenzothbiophene. J. Phys. Org. Chem. 14, 709–715 (2001); b) Alvarado, Y.J., Cubillán, N., Labarca, P.H., Karma, A., Arrieta, F., Castellano, O., Soscún, H.: Static and dynamic dipole polarizabilities of 2- and 3-methylthiophene in solution: experimental and theoretical determination. J. Phys. Org. Chem. 15, 154–164 (2002); c) Alvarado, Y.J., Soscún, H., Velazco. W., Labarca, P.H., Cubillán, N., Hernandez, J.: Dipole polarizability of the pyrazabole molecule in solution. J. Phys. Org. Chem. 15, 835–843 (2002); d) Alvarado, Y.J., Labarca, P.H., Cubillán, N., Osorio, E., Karam, A.: Solvent effect on electronic polarizability of benzonitrile. Z. Naturforsch. 58a, 68–74 (2003); e) Alvarado, Y.J., Peña-Suárez, J.L., Cubillán, N., Labarca, P.H., Caldera-Luzardo, J.A., López-Linares, F.: Influence of the dielectric medium on the carbonyl infrared absorption peak of acetylferrocene. Molecules 10, 457–474 (2005); f) Alvarado, Y.J., Caldera-Luzardo, J., De La Cruz, C., Ferrer-Amado, G., Michelena, E., Silva, P.: Volumetric, electric, and magnetic properties of thioxanthen-9-one in aprotic solvents as revealed by high-precision densitometry, high-accuracy refractometry and magnetic susceptibility measurements and by DFT calculations. J. Solution Chem. 35, 29–49 (2006); g) Soscun, H., Hernández, J., Escobar, R., Toro-Mendoza, C., Alvarado, Y., Hinchliffe, A.: Ab-initio and density functional theory calculations of the dipole polarizability and the second dipole hyperpolarizability of benzene. Int. J. Quant. Chem. 90, 497–506 (2002). 5. a) Kohner, H.: Über die Konzentrationsabhängigkeit der Äquivalentrefraktion von starken Elektrolyten in Lösung. Z. Phys Chem. B1, 427–455 (1928); b) Geffcken, W.: Über die Konzentrationsabhängigkeit der Äquivalentrefraktion von starken Elektrolyten in Lösung. Z. Phys Chem. B5, 81–123 (1929); (c) Grunwald, E., Haley, J.; Acid dissociation constants of trifluoroacetic acid in water measured by differential refractometry. J. Phys. Chem. 72, 1944–1948 (1968).
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