UV/vis absorption and fluorescence spectroscopic study of some new 4- hydroxy-7-methoxycoumarin derivatives. Part I: Effect of substitution by a benzo-1,4-dioxanyl or an ethyl furoate group in the 3-position

New Journal of Chemistry

Volumn 23, Issue 9, 1999, Pages 923-927

  Dondon, Régine ^a   Khilya, Vladimir P ^b   Roshal, Alexander D ^a   Fery Forgues, Suzanne ^a  

^a Université Paul Sabatier   (France)

^b TARAS SHEVCHENKO NATIONAL UNIVERSITY OF KYIV   (Ukraine)

Author keywords

[No Author keywords available]

Indexed keywords

4 HYDROXY 7 METHOXYCOUMARIN; COUMARIN DERIVATIVE; UNCLASSIFIED DRUG;

ABSORPTION SPECTROSCOPY; ARTICLE; CHEMICAL STRUCTURE; FLUORESCENCE SPECTROSCOPY; PRIORITY JOURNAL; TEMPERATURE SENSITIVITY; ULTRAVIOLET SPECTROSCOPY; VISCOSITY;

EID: 0032855166     PISSN: 11440546     EISSN: None     Source Type: Journal    
DOI: 10.1039/a902285f     Document Type: Article

References (23)

1. 1 K. H. Drexhage, J. Res. Nat. Bur. Stand., Sect. A, 1976, 80, 421.
2. 2 K. H. Drexhage, in Dye Lasers. Topics in Applied Physics, ed. F. P. Schäfer, Springer, Berlin, 1973, vol. 1.
3. 3 G. Jones II, W. R. Jackson, C. Choi and W. R. Bergmark, J. Phys. Chem., 1985, 89, 294.
4. 4 R. P. Haugland, Handbook of Fluorescent Probes and Research Chemicals, Molecular Probes, Inc., Eugene, OR, USA, 1992-4.
5. 5 H. Schwander and P. Hendrix, in Ullmann's Encyclopedia of Industrial Chemistry, ed. Y. S. Yamamoto, VCH, Weinheim, 5th edn., 1988, vol. A11, pp. 280-281.
6. 6 H. K. Arora, A. R. Aggarwal and R. P. Singh, Indian J. Chem., Sect. A, 1982, 21, 844.
7. 7 O. S. Wolfbeis, E. Koller and P. Hochmuth, Bull. Chem. Soc. Jpn, 1985, 58, 731 and refs. cited therein.
8. 8 G. G. Guilbault, Enzymatic Methods of Analysis, Pergamon Press, Oxford, 1970, pp. 52 and 62.
9. 9 G. G. Guilbault, Practical Fluorescence. Theory, Methods and Techniques, M. Dekker, New York, 1973, p. 354.
10. 10 J. Boyd, A. Robertson and W. B. Whalley, J. Chem. Soc., 1948, 15, 174 and refs. cited therein.
11. 11 D. H. R. Barton, D. M. X. Donnelly, J. P. Finet and P. H. Stenson, Tetrahedron, 1988, 44, 6387.
12. 12 D. H. R. Barton, D. M. X. Donnelly, J. P. Finet and P. J. Guiry, J. Chem. Soc., Perkin Trans. 1, 1992, 1365.
13. 13 A. Knierzinger and O. S. Wolfbeis, J. Heterocycl. Chem., 1980, 225, 17.
14. 14 C. Reichardt, Solvents and Solvent Effects in Organic Chemistry, VCH, Weinheim, 2nd edn., 1988, p. 408.
15. 15 J. J. Aaron, M. Buna, C. Parkanyi, M. S. Antonious, A. Tine and L. Cisse, J. Fluoresc., 1995, 5, 337.
16. 16 C. Parkanyi, M. S. Antonious, J. J. Aaron, M. Buna, A. Tine and L. Cisse, Spectrosc. Lett., 1994, 27, 439.
17. 17 D. D. Perrin and W. L. F. Armarego, Purification of Laboratory Chemicals, Pergamon, Oxford, 3rd edn., 1988, ch. 3.
18. 18 B. K. Deshmukh and J. F. Coetzee, Anal. Chem., 1984, 56, 2373.
19. 19 W. W. Mantulin and P. Song, J. Am. Chem. Soc., 1973, 95, 5122.
20. 20 O. S. Wolfbeis and G. Uray, Monatsh. Chem., 1978, 109, 123.
21. 21 V. P. Khilya, S. V. Kovalyov, N. S. Miroshnichenko and A. V. Turov, Khim. Prir. Soedin., 1998, 1, 45.
22. 22 A. Aitmambetov and V. P. Khilya, Khim. Prir. Soedin., 1994, 2, 226.
23. 23 G. A. Reynolds and K. H. Drexhage, Opt. Commun., 1975, 13, 222.