Multiparametric probing of intermolecular interactions with fluorescent dye exhibiting excited state intramolecular proton transfer

Physical Chemistry Chemical Physics

Volumn 5, Issue 3, 2003, Pages 461-468

  Klymchenko, Andrey S ^a,b   Demchenko, Alexander P ^a,c  

^a SCIENTIFIC AND TECHNOLOGICAL RESEARCH COUNCIL OF TURKEY   (Turkey)

^b TARAS SHEVCHENKO NATIONAL UNIVERSITY OF KYIV   (Ukraine)

^c PALLADIN INSTITUTE OF BIOCHEMISTRY   (Ukraine)

Author keywords

[No Author keywords available]

Indexed keywords

FLAVONE DERIVATIVE; FLUORESCENT DYE;

ABSORPTION; ARTICLE; CHEMICAL PARAMETERS; HYDROGEN BOND; MICROENVIRONMENT; MOLECULAR INTERACTION; PHYSICAL CHEMISTRY; POLARIZATION; PROTON TRANSPORT; SPECTROSCOPY;

EID: 0037208160     PISSN: 14639076     EISSN: None     Source Type: Journal    
DOI: 10.1039/b210352d     Document Type: Article

References (48)

1. E. L. Lippert, in Organic Molecular Photophysics, ed. J. B. Birks, Wiley, New York, 1975, vol. 2, p. 1.
2. W. Liptay, in Excited States, ed. E. C. Lim, Academic Press, New York, 1974, p. 129.
3. N. Mataga, T. Kubata, Molecular Interactions and Electronic Spectra, M. Dekker, New York, 1970.
4. N. G. Bakhshiev, Spectroscopy of Intermolecular Interactions, Nauka, Leningrad, 1972.
5. P. Suppan, N. Ghoneim, Solvatochromism, Royal Society of Chemistry, Cambridge, UK, 1997.
6. C. Reichardt, Chem. Rev., 1994, 94, 2319.
7. D. C. Dong and M. A. Winnik, Can. J. Chem., 1984, 62, 2560.
8. J.-C. Del Valle and J. Catalan, Chem. Phys., 2001, 270, 1.
9. M. J. Kamlet, C. Dickinson and R. W. Taft, Chem. Phys. Lett., 1981, 77, 69.
10. M. H. Abraham, J. Phys. Org. Chem., 1993, 6, 660.
11. M. H. Abraham, H. S. Chadha, G. S. Whiting and R. C. Mitchell, J. Pharmacol. Sci., 1994, 83, 1085.
12. P. K. Sengupta and M. Kasha, Chem. Phys. Lett., 1979, 68, 382.
13. T. C. Swiney and F. D. Kelley, J. Chem. Phys., 1993, 99, 211.
14. P.-T. Chou, M. L. Martinez and J. H. Clements, J. Phys. Chem., 1993, 97, 2618.
15. S. J. Formosinho and L. G. Arnaut, J. Photochem. Photobiol. A: Chem., 1993, 75, 21.
16. A. Mordzinski and W. Kühnle, J. Phys. Chem., 1986, 90, 1455.
17. A. Douhal, F. Amat-Guerri, M. P. Lillo and A. U. Acuna, Photochem. Photobiol A: Chem., 1994, 78, 127.
18. N. A. Nemkovich, W. J. Baumann and V. G. Pivovarenko, J. Photochem. Photobiol. A: Chem., 2002, 153, 19.
19. A. P. Demchenko, S. Ercelen, A. D. Rochal and A. S. Klymchenko, Pol. J. Chem., 2002, 76, 1287.
20. S. Ercelen, A. S. Klymchenko and A. P. Demchenko, Anal. Chim. Acta., 2002, 464, 273.
21. W. Liu, Y. Wang, W. Jin, G. Shen and R. Yu, Anal. Chim. Acta, 1999, 383, 299.
22. A. S. Klymchenko and A. P. Demchenko, Langmuir, 2002, 18, 5637.
23. A. D. Roshal, A. V. Grigorovich, A. O. Doroshenko, V. G. Pivovarenko and A. P. Demchenko, J. Phys. Chem. A, 1998, 102, 5907.
24. A. S. Klymchenko and A. P. Demchenko, J. Am. Chem. Soc., 2002, 124, 12 372.
25. O. P. Bondar, V. G. Pivovarenko and E. S. Rowe, Biochem. Biophys. Acta, 1998, 1369, 119.
26. G. Duportail, A. S. Klymchenko, Y. Mely and A. P. Demchenko, FEBS Lett., 2001, 508, 196.
27. G. Duportail, A. S. Klymchenko, Y. Mely and A. P. Demchenko, J. Fluoresc., 2002, 12, 181.
28. A. S. Klymchenko, G. Duportail, T. Ozturk, V. G. Pivovarenko, Y. Mély and A. P. Demchenko, Chem. Biol., 2002, 9, 1199.
29. D. B. Siano and D. E. Metzler, J. Chem. Phys., 1969, 51, 1856.
30. J. Catalan, J.-C. del Valle, C. Diaz, J. Palomar, J. L. G. De Paz and M. Kasha, Int. J. Quantum Chem., 1999, 72, 421.
31. A. S. Klymchenko, V. G. Pivovarenko, A. P. Demchenko, Spectrochim. Acta, Part A, 2003, in press.
32. The behaviour of the parent 3-hydroxyflavone is probably different. See discussion on its H-bonding effects in G. F. Woolfe and P. J. Thistlethwaite, J. Am. Chem. Soc., 1981, 103, 6916; A. J. G. Strandjord and P. F. Barbara, J. Phys. Chem., 1985, 89, 2355; G. A. Brucker and D. F. Kelley, J. Phys. Chem., 1987, 91, 2862.
33. The behaviour of the parent 3-hydroxyflavone is probably different. See discussion on its H-bonding effects in G. F. Woolfe and P. J. Thistlethwaite, J. Am. Chem. Soc., 1981, 103, 6916; A. J. G. Strandjord and P. F. Barbara, J. Phys. Chem., 1985, 89, 2355; G. A. Brucker and D. F. Kelley, J. Phys. Chem., 1987, 91, 2862.
34. The behaviour of the parent 3-hydroxyflavone is probably different. See discussion on its H-bonding effects in G. F. Woolfe and P. J. Thistlethwaite, J. Am. Chem. Soc., 1981, 103, 6916; A. J. G. Strandjord and P. F. Barbara, J. Phys. Chem., 1985, 89, 2355; G. A. Brucker and D. F. Kelley, J. Phys. Chem., 1987, 91, 2862.
35. N. Ghoneim, Spectrochim. Acta, Part A, 2001, 57, 1877.
36. W. E. Acree, D. C. Wilkins, S. A. Tucker, J. M. Griffin and J. R. Powel, J. Phys. Chem., 1994, 98, 2537.
37. D. E. Wetzler, C. Chesta, R. Fernandez-Prini and P. F. Aramendia, J. Phys. Chem. A., 2002, 106, 2390.
38. Y.-C. Jean and H. J. Ache, J. Am. Chem. Soc., 1978, 100, 6320.
39. A. Datta, D. Mandal, S. K. Pal and K. Bhattacharyya, J. Phys. Chem. B., 1997, 101, 10 221.
40. K. M. Manoj, R. Jayakumar and S. K. Rakshit, Langmuir, 1996, 12, 4068.
41. B. Sengupta and P. Sengupta, Biochem. Biophys. Res. Commun., 2000, 277, 13.
42. A. P. Demchenko, Biochim. Biophys. Acta., 1994, 1209, 149. These data were recently reproduced and extended by S. Ercelen et al. (unpublished). Experimental conditions: 50 mM phosphate buffer, pH = 7.0; protein and probe concentrations were 1 μM and 0.5 μM, respectively.
43. A. Sytnik, D. Gormin and M. Kasha, Proc. Natl. Acad. Sci. USA, 1994, 91, 11 968.
44. J. Guharay, B. Sengupta and P. K. Sengupta, Proteins, 2001, 43, 75.
45. D. Carter and J. X. Ho, Adv. Protein Chem., 1994, 45, 153.
46. A. S. Klymchenko, T. Ozturk, V. G. Pivovarenko and A. P. Demchenko, Can. J. Chem., 2001, 79, 358.
47. A. S. Klymchenko, T. Ozturk, V. G. Pivovarenko and A. P. Demchenko, Tetrahedron Lett., 2001, 42, 7967.
48. A. S. Klymchenko, T. Ozturk and A. P. Demchenko, Tetrahedron Lett., 2002, 43, 7079.