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The Synthesis of New Porphyrin–Quinone Dyad Systems

Russian Journal of Bioorganic Chemistry volume 27, pages 50–56 (2001)Cite this article

Abstract

New porphyrin–quinone dyad systems containing spacer groups of various lengths and structures and sterically hindered 5,10,15,20-tetrakis(3,5-di-tert-butylphenyl)porphyrin as an electron donor were synthesized. These compounds seem to be promising models for studying the photoinduced electron transfer.

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REFERENCES

  1. Evstigneeva, R.P. and Gribkov, A.A., Izv. Ross. Akad. Nauk, Ser. Khim., 1996, no. 1, pp. 9-24.

    Google Scholar 

  2. Shreiber, M., Fuchs, C., and Scholz, R., J. Lumin., 1998, nos. 76-77, pp. 482-485.

    Google Scholar 

  3. Rempel, U., Meyer, S., Maltzan, B., and Borczyskowski, C., J. Lumin., 1998, no. 78, pp. 97-110.

    Google Scholar 

  4. Hyslop, A.G. and Therien, M.J., Inorg. Chim. Acta, 1998, nos. 275-276, pp. 427-434.

    Google Scholar 

  5. Sen, A. and Krishnan, V., J. Photochem. Photobiol., A: Chem., 1999, no. 123, pp. 77-85.

    Google Scholar 

  6. Hayashi, Sh. and Kato, Sh., J. Phys. Chem., A, 1998, vol. 102, pp. 3333-3342.

    Google Scholar 

  7. Yamazaki, T., Yamazaki, I., and Osuka, A., J. Phys. Chem., A, 1998, vol. 102, pp. 7858-7865.

    Google Scholar 

  8. Efimov, A.V., Anikin, M.V., Tkachenko, N.V., Mironov, A.F., and Lemmetyinen, H., Chem. Phys. Lett., 1998, vol. 289, pp. 572-578.

    Google Scholar 

  9. Tkachenko, N.V., Tauber, A.Y., Lemmetyinen, H., and Hyinnen, P.H., Thin Solid Films, 1996, vol. 280, pp. 244-248.

    Google Scholar 

  10. Anikin, M.V., Tkatchenko, N.V., and Lemmetyinen, H., Langmuir, 1997, vol. 13, pp. 3002-3008.

    Google Scholar 

  11. Ponomarev, G.V. and Yashunskii, V.G., USSR Inventor's Certificate no. 458 551, Byull. Izobret., 1975, no. 4, p. 51.

    Google Scholar 

  12. Maravin, G.B., Ponomarev, G.V., Yashunskii, V.G., and Morlyan, N.M., USSR Inventor's Certificate no. 891673, Byull. Izobret., 1981, no. 47, p. 109.

    Google Scholar 

  13. Rumyantseva, V.D., Aksenova, E.A., Ponamoreva, O.N., and Mironov, A.F., Bioorg. Khim., 2000, vol. 26, pp. 471-477.

    Google Scholar 

  14. Makarov, V.A., Filippovich, E.I., and Evstigneeva, R.P., Khim. Geterotsikl. Soedin., 1987, no. 9, pp. 1194-1199.

    Google Scholar 

  15. Adler, A.D., Longo, F.R., and Finarelli, J.D., J. Org. Chem., 1967, vol. 32, pp. 476-478.

    Google Scholar 

  16. Bach, G. and Kjaer, H., Acta Chem. Scand., 1971, vol. 25, pp. 2632-2641.

    Google Scholar 

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Authors and Affiliations

  1. Lomonosov State Academy of Fine Chemical Technology, pr. Vernadskogo 86, Moscow, 117571, Russia

    E. A. Aksenova & A. F. Mironov

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  1. E. A. Aksenova
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  2. A. F. Mironov
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Aksenova, E.A., Mironov, A.F. The Synthesis of New Porphyrin–Quinone Dyad Systems. Russian Journal of Bioorganic Chemistry 27, 50–56 (2001). https://doi.org/10.1023/A:1009583203239

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  • DOI: https://doi.org/10.1023/A:1009583203239

  • dyads
  • photoinduced electron transfer
  • porphyrin
  • porphyrin–quinone