Preferential solvation and solvatochromic behaviour of quinoline in binary alkan-1-ol/N,N-dimethylformamide solvent mixtures

Journal of Molecular Liquids

Volumn 136, Issue 1-2, 2007, Pages 15-21

  Moita, M L ^a   Teodoro, R A ^a   Pinheiro, L M ^b  

^a UNIVERSITY OF LISBON   (Portugal)

^b RESEARCH INSTITUTE FOR MEDICINES IMED ULISBOA   (Portugal)

Author keywords

Alkan 1 ol N,N dimethylformamide binary mixtures; Preferential solvation model; Quinoline; Solvatochromism; Synergism

Indexed keywords

CYCLOHEXANE; DIMETHYLFORMAMIDE; ENERGY TRANSFER; METHANOL; SOLVATION; SOLVENTS; ULTRAVIOLET SPECTROSCOPY;

PREFERENTIAL SOLVATION MODEL; QUINOLINE; SOLVATOCHROMISM; SYNERGISM;

NITROGEN COMPOUNDS;

EID: 34748855579     PISSN: 01677322     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molliq.2006.12.023     Document Type: Article

References (35)

1. Barton D., and Ollis W.D. Comprehensive Organic Chemistry, The Synthesis and Reactions of Organic Compounds vol. 4 (1979), Pergamon Press, Oxford/UK 166
2. Egan T.J., Ross D.C., and Adams P.A. FEBS Lett. 352 (1994) 54
3. Desai P.K., Desai P., Machhi D., Desai C.M., and Patel D. Indian J. Chem. 35B (1996) 871
4. Hirano Y., Uehara M., Saeki K., Kato T., Takahashi K., and Mizutani T. J. Health Sci. 48 (2002) 118
5. Souza M.V., and Vasconcelos T.R.A. Quim. Nova 28 (2005) 678
6. Santo M., Cattana R., and Silber J.J. Spectrochim. Acta 57A (2001) 1541
7. Yang R., and Schulman G. Luminescence 16 (2001) 129
8. Crépin C., Dubois V., Goldfarb F., Chaput F., and Boilot J.P. Phys. Chem. Chem. Phys. 7 (2005) 1933
9. Reichardt C. Solvents and Solvent Effects in Organic Chemistry. 2nd ed. (1988), Wiley-VCH, Weinheim 285
10. Reichardt C. Chem. Soc. Rev. 21 (1992) 147
11. Boggetti H., Anunziata J.D., Cattana R., and Silber J.J. Spectrochim. Acta 50A (1994) 719
12. Mancini P.M., Terenzani A., Adam C., del C. Pérez A., and Vottero L.R. J. Phys. Org. Chem. 12 (1999) 713
13. Ali A., Nain A.K., and Kamil M. Thermochim. Acta 274 (1996) 209
14. Garcia B., Alcalde R., Leal J.M., and Matos J.S. J. Chem. Soc., Faraday Trans. 93 (1997) 1115
15. Bai T.-C., Yao J., and Han S.-J. Fluid Phase Equilib. 152 (1998) 283
16. Zielkiewicz J. Phys. Chem. Chem. Phys. 2 (2000) 2925
17. Stangret J., Kamieñska-Piotrowicz E., and Szymañska-Cybulska J. Spectrochim. Acta 61A (2005) 3043
18. Yu L., Zhu Y., Hu X.-G., and Pang X.-H. J. Chem. Eng. Data 51 (2006) 1110
19. Skwierczynski R., and Connors K.A. J. Chem. Soc., Perkin Trans. 2 (1994) 467
20. Rosés M., Ràfols C., Ortega J., and Bosch E. J. Chem. Soc., Perkin Trans. 2 (1995) 1607
21. Ortega J., Ràfols C., Bosch E., and Rosés M. J. Chem. Soc., Perkin Trans. 2 (1996) 1497
22. Ràfols C., Rosés M., and Bosch E. J. Chem. Soc., Perkin Trans. 2 (1997) 243
23. Wróblewska E.K., Soroka J.A., Soroka K.B., and Ga{ogonek}siorowska M. J. Phys. Org. Chem. 18 (2005) 347
24. Silva L., Machado C., and Rezende M.C. J. Chem. Soc., Perkin Trans. 2 (1995) 483
25. Rezende M.C. J. Braz. Chem. Soc. 8 (1997) 631
26. Reichardt C. Chem. Rev. 94 (1994) 2319
27. Marcus Y. Solvent Mixtures (2002), Marcel Dekker, New York, Basel 98 pp.
28. Kamlet M.J., Abboud J.-L.M., Abraham M.H., and Taft R.W. J. Org. Chem. 48 (1983) 2877
29. Osada M., Toyoshima K., Mizutani T., Minami K., Watanabe M., Adschiri T., and Aral K. J. Chem. Phys. 118 (2003) 4573
30. Garcia B., Alcalde R., Leal J.M., and Trenzado J.L. J. Phys. Org. Chem. 10 (1997) 138
31. Chao J.P., Dai M., and Wang Y.X. J. Chem. Thermodyn. 21 (1989) 1169
32. Wang C., Li H., Zhu L., and Han S. J. Solution Chem. 31 (2002) 109
33. Mancini P.M.E., Terenzani A., Adam C., and Vottero L.R. J. Phys. Org. Chem. 10 (1997) 849
34. Herodes K., Leito I., Koppel I., and Rosés M. J. Phys. Org. Chem. 12 (1999) 109
35. Manin N.G., Belichenko S.Y., and Korolev V.P. Russ. J. Gen. Chem. 73 (2003) 9