Intramolecular exciplex formation and non-radiative quenching in alternating copolymer of 2-vinylnaphthalene and 2-(dimethylamino)ethyl methacrylate in dilute solution

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Y. Itoh, M. Inoue, Y. Ohbayashi and S. Suzuki


Abstract

Alternating and random copolymers of 2-vinylnaphthalene and 2-(dimethylamino)ethyl methacrylate have been synthesized. The random copolymers showed both excimer and exciplex emissions in 1,4-dioxane, the former of which became more important with increasing naphthyl content in the copolymer. For the alternating copolymer, in contrast, an exciplex emission but no discernible excimer emission was observed. This indicates negligible interaction between naphthyl chromophores and complex formation between neighbouring naphthyl and 2-(dimethylamino)ethyl groups. However, additional quenching still occurs in the alternating copolymer, which may be attributed to the interaction of two amino groups with the excited naphthalene. Introduction of unreactive monomers into the copolymer and separation of the dimethylamino groups from the polymer main chain are found to be effective in reducing the extra quenching.


References

  1. R. F. Reid and I. Soutar, J. Polym. Sci. Polym. Phys. Ed., 1978, 16, 23 Search PubMed.
  2. S. E. Webber, Chem. Rev., 1990, 90, 1469 CrossRef CAS.
  3. Y. Itoh, M. Nakada, H. Satoh, A. Hachimori and S. E. Webber, Macromolecules, 1993, 26, 1941 CrossRef CAS.
  4. Y. Itoh, M. Inoue, T. Takahashi, A. Hachimori and S. Suzuki, J. Polym. Sci. Polym. Chem. Ed., 1995, 33, 1069 CAS.
  5. Y. Itoh, M. Inoue, A. Hachimori and K. Abe, Polym. Adv. Tech., 1997, 8, 35 Search PubMed.
  6. K. Iwai, K. Yamamoto, F. Takemura, M. Furue and S. Nozakura, Macromolecules, 1985, 18, 1021 CrossRef CAS.
  7. S. Tazuke, Makromol. Chem. Suppl., 1985, 56, 1269 Search PubMed.
  8. Y. Iwaya and S. Tazuke, Macromolecules, 1982, 15, 396 CrossRef CAS.
  9. Y. Itoh, K. Ogura, T. Hirota, A. Hachimori and K. Abe, Acta Polym., 1997, 48, 164 CAS.
  10. H. Satozono, S. Suzuki, N. Tokou, H. Takehara and Y. Uno, Nippon Kagaku Kaishi, 1994, 115 CAS.
  11. P. Blin, C. Bunel and E. Marechal, J. Polym. Sci. Polym. Chem. Ed., 1981, 19, 891 CAS.
  12. R. B. Fox, T. R. Price, R. F. Cozzens and W. H. Echols, Macromolecules, 1974, 7, 937 CrossRef CAS.
  13. F. Bai, C. H. Chang and S. E. Webber, Macromolecules, 1986, 19, 588 CrossRef CAS.
  14. S. P. Van and G. S. Hammond, J. Am. Chem. Soc., 1978, 100, 3895 CrossRef CAS.
  15. R. A. Beecroft, R. S. Davidson and T. D. Whelan, J. Chem. Soc., Chem. Commun., 1978, 911 RSC.
  16. R. A. Beecroft, R. S. Davidson, D. Goodwin and J. E. Pratt, Pure Appl. Chem., 1982, 54, 1605 CAS.
  17. H. Beens and A. Weller, Chem. Phys. Lett., 1968, 2, 140 CrossRef CAS.
  18. D. Creed and R. A. Caldwell, J. Am. Chem. Soc., 1974, 96, 7369 CrossRef CAS.
  19. T. Mimura, M. Itoh, T. Ohta and T. Okamoto, Bull. Chem. Soc. Jpn., 1977, 50, 1665 CAS.
  20. Ph. Van Haver, N. Helsen, S. Depaemelaere, M. Van der Auweraer and F. C. De Schryver, J. Am. Chem. Soc., 1991, 113, 6849 CrossRef CAS.
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