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Luminescence characteristics of new substituted coumarins

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Journal of Applied Spectroscopy Aims and scope

Fluorescence spectra at 298 and 77 K and phosphorescence spectra at 77 K have been measured for five new compounds. Fluorescence and phosphorescence quantum yields have been measured by comparison with a standard (8-methoxypsoralen). Phosphorescence lifetimes at 77 K have been found for 2-hydrazyl-3,4-cyclopentyl-14,14-dimethylpryanocoumarin (1.60 msec); 2-hydrazyl-3,4-cyclohexyl-7-methoxycoumarin (1.35); 3,4-phenyl-4′,5′-cyclohexylpsoralen (2.50); 4′-methyl-3,4-cycloheptylpsoralen (1.10); and 4′,5′-dimethyl-3,4-cyclohexylpsoralen (1.25). The basic channel of energy deactivation for 3,4-phenyl-4′,5′-cyclohexylpsoralen; 4′-methyl-3,4-cycloheptylpsoralen; and 4′,5′-dimethyl-3,4-cyclohexylpsoralen is radiative transfer. Energies of the lowest excited triplet states have been calculated using an INDO/S quantum-chemical method.

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References

  1. A. Ya. Potapenko and A. A. Kyagova, in: Proceedings of the IVth Convention of Photobiologists [in Russian], Sept. 26–30, 2005, Saratov, Izd. Saratov Gos. Univ. (2005), 161–164.

  2. C. Tablet, A. Jelea, and M. Hillebrand, J. Photochem. Photobiol. A: Chem., 183, No. 1–2, 89–97 (2006).

    Article  Google Scholar 

  3. H. Honigsmann, T. B. Fitzpatrick, M. A. Pathak, and K. Wolff, Dermatology in General Medicine, McGraw-Hill, New York (1993), Vol. 1, 1728–1754.

    Google Scholar 

  4. A. D. Mulla, N. N. Math, and M. I. Savadatti, Praman, 36, No. 6, 639–645 (1991).

    Article  ADS  Google Scholar 

  5. T.-I. Lai, B. T. Lim, and E. C. Lim, J. Am. Chem. Soc., 104, No. 26, 7631–7635 (1982).

    Article  Google Scholar 

  6. W. W. Mantulin and P.-S. Song, J. Chem. Soc., 95, No. 16, 5122–5129 (1973).

    Article  Google Scholar 

  7. G. S. Han, D. J. Yoo, S. K. Kim, S. C. Shim, and H. K. Kang, Photochem. Photobiol., 64, No. 3, 525–530 (1996).

    Article  Google Scholar 

  8. C. A. Parker, Photoluminescence of Solutions with Applications to Photochemistry and Analytical Chemistry, Elsevier, New York (1968).

    Google Scholar 

  9. H. Turki, S. Abid, R. El Gharbi, and S. Fery-Forgues, C. R. Chim., 9, No. 10, 1252–1259 (2006).

    Google Scholar 

  10. M. E. Solov’ev and M. M. Solov’ev, Computer Chemistry [in Russian], SOLON-Press, Moscow (2005), 346–350.

    Google Scholar 

  11. G. V. Mayer, V. Ya. Artyukhov, O. K. Bazyl’, T. N. Kopylova, R. T. Kuznetsova, N. R. Rib, and I. V. Sokolova, Electronically Excited States and Photochemistry of Organic Compounds [in Russian], Nauka, Novosibirsk (1997).

    Google Scholar 

  12. N. Yu. Vasil’eva, I. V. Sokolova, L. G. Samsonova, T. N. Kopylova, and G. V. Mayer, J. Fluoresc., 9, No. 1, 17–25 (1999).

    Article  Google Scholar 

  13. G. V. Mayer and V. Ya. Artyukhov, Dokl. Akad. Nauk Vyssh. Skh. Ross., 2, No. 3, 1–10 (2004).

    Google Scholar 

  14. N. G. Bryantseva, I. V. Sokolova, A. B. Tsyrenzhapova, N. I. Selivanov, V. P. Khilya, and Ya. L. Garazd, Zh. Prikl. Spektrosk., 75, No. 5, 694–699 (2008).

    Google Scholar 

  15. S. C. Shim and G. S. Han, Photochem. Photobiol., 66, No. 2, 156–163 (1997).

    Article  Google Scholar 

  16. S. S. Sastry, B. M. Ross, and A. P’arragas, J. Biol. Chem., 272, No. 6, 3715–3723 (1997).

    Google Scholar 

  17. P.-S. Song and W. H. Gordon III, J. Phys. Chem., 74, No. 24, 4234–4240 (1970).

    Article  Google Scholar 

  18. J. F. Rabek, Experimental Methods in Photochemistry and Photophysics, Wiley, Chichester, New York (1982).

    Google Scholar 

  19. V. L. Ermolaev and E. B. Sveshnikova, Acta Phys. Pol., 34, 771–790 (1968).

    Google Scholar 

  20. N. J. Turro, Molecular Photochemistry, Benjamin, New York (1965).

    Google Scholar 

  21. N. G. Bryantseva, Proc. SPIE Int. Soc. Opt. Eng., 6522, 652201-1–652201-6 (2006).

    ADS  Google Scholar 

  22. N. E. Koval?skaya, N. A. Kuznetsova, and I. V. Sokolova, Opt. Atm. Okeana, 17, No. 2–3, 221–224 (2004).

    Google Scholar 

  23. M. Craw, R. V. Bensasson, J. C. Ronfard-Haret, M. T. S. E. Melo, and T. G. Truscott, Photochem. Photobiol., 37, No. 6, 611–615 (1983).

    Article  Google Scholar 

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Correspondence to N. G. Bryantseva.

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Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 76, No. 6, pp. 862–868, November–December, 2009.

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Bryantseva, N.G., Sokolova, I.V., Gadirov, R.M. et al. Luminescence characteristics of new substituted coumarins. J Appl Spectrosc 76, 813–818 (2009). https://doi.org/10.1007/s10812-010-9280-1

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  • DOI: https://doi.org/10.1007/s10812-010-9280-1

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