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Polar and Hydrogen-Bonding Effects of Alcohols on the Emission Spectrum of Styrene–Triethylamine System

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Abstract

The emission spectra of styrene (ST)–triethylamine (TEA) systems were measured under steady-state illumination conditions in some tetrahydrofuran (THF)–protic solvent mixtures. The fluorescence spectrum of the ST–TEA system in THF consists of two bands (band A at 304 nm (fluorescence of ST) and band B at 460 nm (emission from an exciplex)). The intensity of band A increased and that of band B decreased with increasing amounts of protic solvents in THF–protic solvent mixtures. The increase in the intensity of band A was explained by the decrease in the concentration of free amine owing to the hydrogen-bonding interaction (or protonation) between TEA and protic solvents. The decrease in the intensity of band B was considered to be caused by the decrease in the concentration of free amine upon the addition of protic solvents and the enhanced conversion of the exciplex to an ion pair with increasing solvent polarity. The polar effect was expressed as a function of the relative permittivity of the solution.

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References

  1. H. Knibbe, D. Rehm, and A. Weller, Ber. Bunsen Ges. Phys. Chem. 72, 257 (1968).

    CAS  Google Scholar 

  2. E. A. Chandross and H. T. Thomas, Chem. Phys. Lett. 9, 393 (1971).

    CAS  Google Scholar 

  3. M. M. Hui and W. R. Ware, J. Am. Chem. Soc. 98, 4712 (1976).

    Google Scholar 

  4. A. M. Halpern, J. Am. Chem. Soc. 106, 6484 (1984).

    CAS  Google Scholar 

  5. A. M. Swinnen, M. Van der Auweraer, and F. C. De Schryver, J. Photochem. 28, 315 (1985).

    Article  CAS  Google Scholar 

  6. S. Matsuzawa, M. Lamotte, P. Garrigues, and Y. Shimizu, J. Phys. Chem. 98, 7832 (1994).

    CAS  Google Scholar 

  7. D. P. Andrews, G. S. Beddard, and B. J. Whitaker, J. Phys. Chem. A 104, 7785 (2000).

    CAS  Google Scholar 

  8. S. P. Van and G. S. Hammond, J. Am. Chem. Soc. 100, 3895 (1978).

    Article  CAS  Google Scholar 

  9. A. T. Amos and B. L. Burroughs, Adv. Quantum Chem. 7, 289 (1973).

    CAS  Google Scholar 

  10. A. M. Halpern and S. L. Frye, J. Phys. Chem. 92, 6620 (1988).

    Article  CAS  Google Scholar 

  11. S. Oh and Y. Shirota, J. Photochem. Photobiol. A 92, 79 (1995).

    CAS  Google Scholar 

  12. S. Oh, Y. Shirota, H. Mikawa, and S. Kusabayashi, Chem. Lett. 2121 (1986).

  13. S. Yamamoto, G. Xie, M. Nakamura, and Y. Sueishi, Chem. Lett. 760 (2002).

  14. G. Xie, M. Nakamura, Y. Sueishi, and S. Yamamoto, J. Photochem. Photobiol. A 162, 73 (2004).

    CAS  Google Scholar 

  15. G. Xie, Y. Sueishi, and S. Yamamoto, J. Photochem. Photobiol. A 162, 449 (2004).

    CAS  Google Scholar 

  16. G. Xie, Y. Sueishi, and S. Yamamoto, J. Fluores. (in press).

  17. R. J. Brentnall, P. M. Crosby, and K. Salisbury, J. Chem. Soc. Perkin Trans. 2, 2002 (1977).

    Google Scholar 

  18. F. D. Lewis, G. D. Reddy, S. Schneider, and M. Gahr, J. Am. Chem. Soc. 113, 3498 (1991).

    CAS  Google Scholar 

  19. F. D. Lewis, G. D. Reddy, D. Bassani, S. Schneider, and M. Gahr, J. Photochem. Photobiol. A 65, 205 (1992).

    CAS  Google Scholar 

  20. F. D. lewis and D. M. Bassani, J. Photochem. Photobiol. A 66, 43 (1992).

    CAS  Google Scholar 

  21. J.-C. Mai, Y.-C. Lin, T.-M. Hseu, and T.-I. Ho, J. Photochem. Photobiol. A 71, 237 (1993).

    CAS  Google Scholar 

  22. A. Weller, Z. Phys. Chem. 133, 93 (1982).

    CAS  Google Scholar 

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Correspondence to Shunzo Yamamoto.

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Siqintuya, Sueishi, Y. & Yamamoto, S. Polar and Hydrogen-Bonding Effects of Alcohols on the Emission Spectrum of Styrene–Triethylamine System. J Solution Chem 34, 1109–1119 (2005). https://doi.org/10.1007/s10953-005-7690-0

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  • DOI: https://doi.org/10.1007/s10953-005-7690-0

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