Complexation of thallium(I) with adenosine 5′-monophosphate in aqueous methanol solutions

Analytical Sciences

Volumn 21, Issue 8, 2005, Pages 945-949

  Gharib, Farrokh ^a   Kheradman, Tahereh ^a   Amani, Parisa ^a  

^a SHAHID BEHESHTI UNIVERSITY   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALINITY; COMPLEXATION; HYDROGEN BONDS; INORGANIC COMPOUNDS; IONIC STRENGTH; METHANOL; SODIUM COMPOUNDS;

AQUEOUS METHANOL SOLUTIONS; FORMATION CONSTANTS; HYDROGEN BOND DONORS; POLARIZABILITIES; POTENTIOMETRIC TECHNIQUE; SINGLE PARAMETER; SINGLE-PARAMETER CORRELATION; SODIUM PERCHLORATE;

THALLIUM COMPOUNDS;

EID: 27644486772     PISSN: 09106340     EISSN: 13482246     Source Type: Journal    
DOI: 10.2116/analsci.21.945     Document Type: Article

References (36)

1. A. Ben-Naim, "Hydrophobic Interactions", 1980, Plenum, New York.
2. L. R. Pratt, Annu. Rev. Phys. Chem., 1985, 36, 433.
3. G. Desimoni, G. Faita, and P. P. Righetti, Tetrahedron, 1991, 47, 5857.
4. C. Cativiela, J. I. Garcia, J. A. Mayoral, A. J. Royo, L. Salvatella, X. Assfeld, and M. F. Ruiz-Lopez, Tetrahedron: Asymmetry, 1993, 4, 1613.
5. M. F. Ruiz-Lopez, X. Assfeld, J. I. Garcia, J. A. Mayoral, and L. Salvatella, J. Am. Chem. Soc., 1993, 115, 8780.
6. M. Roses, U. Buhvestov, C. Rafols, F. Rived, and E. Bosch, J. Chem. Soc. Perkin Trans., 1997, 2, 1341.
7. U. Buhvestov, F. Rived, C. Rafols, E. Bosch, and M. Roses, J. Phys. Org. Chem., 1998, 11, 185.
8. F. Gharib, J. Chem. Eng. Data, 2005, 50, 196.
9. C. Reichardt, "Solvents and Solvent Effects in Organic Chemistry", 1990, VCH, New York.
10. T. M. Krygowski and W. R. Fawcett, J. Am. Chem. Soc., 1975, 97, 2143.
11. C. G. Swain, M. S. Swain, A. L. Powell, and S. Alunni, J. Am. Chem. Soc., 1983, 105, 502.
12. M. J. Kamlet and R. W. Taft, J. Am. Chem. Soc., 1976, 98, 377.
13. M. J. Kamlet, M. Abbound, M. H. Abraham, and R. W. Taft, J. Org. Chem., 1983, 48, 2877.
14. H. Sigel, F. Hofstetter, R. B. Martin, R. M. Milburn, and K. H. Scheller, J. Am. Chem. Soc., 1984, 106, 7935.
15. H. Sigel, Eur. J. Biochem., 1987, 165, 65.
16. A. G. Rauws, Naunyn-Schmiedeberg's Arch. Pharmacol., 1974, 284, 295.
17. F. Gharib, K. Zare, M. Habibi, and A. Taghvamanesh, Main Group Met. Chem., 2002, 25, 283.
18. L. Lomozik and A. Gasowska, J. Inorg. Biochem., 1996, 62, 103.
19. N. S. Hush and I. R. Reimers, Chem. Rev., 2000, 100, 775.
20. M. R. Gholami and A. H. Yangieh, Int. J. Chem. Kinet., 2001, 118.
21. F. Gharib and M. Vadi, Russ. J. Inorg. Chem., 2002, 47, 1926.
22. Y. Marcus, J. Chem. Soc. Perkin Trans., 1994, 2, 1015.
23. U. Mayer, Pure Appl. Chem., 1979, 51, 1697.
24. T. M. Krygowski and W. R. Fawcett, Can. J. Chem., 1976, 54, 2383.
25. R. W. Taft, J. M. Abbound, M. J. Kamlet, and M. H. Abraham, J. Solution Chem., 1985, 14, 153.
26. V. Gutmann and E. Wychera, Inorg. Nucl. Chem. Lett., 1996, 2, 257.
27. P. Lagrange, M. Schneider, K. Zare, and J. Lagrange, Polyhedron, 1994, 13, 861.
28. L. G. Van Uitert and C. G. Hass, J. Am. Chem. Soc., 1953, 75, 451.
29. H. Sigel, S. S. Massoud, and N. A. Corfu, J. Am. Chem. Soc., 1994, 116, 2958.
30. H. Sigel, S. S. Massoud, and R. Tribolet, J. Am. Chem. Soc., 1988, 110, 6857.
31. M. M. Taqui Khan and A. E. Martel, J. Am. Chem. Soc., 1967, 89, 5585.
32. P. S. Gentile and M. Cefola, J. Am. Chem. Soc., 1963, 67, 1083.
33. N. A. Corfu and H. Sigel, Eur. J. Biochem., 1991, 199, 659.
34. H. Sigel, Chem. Soc. Rev., 1993, 22, 255.
35. D. C. Harris, J. Chem. Edu., 1998, 75, 119.
36. T. M. Krygowski, P. K. Wrona, and M. Zielkowska, Tetrahedron, 1985, 41, 4519.