Theoretical and Experimental Chemistry

, Volume 15, Issue 1, pp 51–55 | Cite as

Stereoisomeric conversions of ketocyanine dyes

  • G. G. Dyadyusha
  • A. A. Rykov
  • Yu. L. Slominskii
Brief Communications


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Literature cited

  1. 1.
    G. G. Dyadyusha, A. A. Rykov, and Yu. L. Slominskii, “Photoisomerization of ketocyanines,” Teor. Eksp. Khim., 14, No. 4, 539–541 (1977).Google Scholar
  2. 2.
    W. West, S. Pearse, and F. Grum, “Stereoisomerism in cyanine dyes: meso-substituted thiacarbocyanines,” J. Phys. Chem., 71, No. 5, 1316–1326 (1967).Google Scholar
  3. 3.
    V. G. Mitina, “Investigation of the photoisomerization of chalcone, its 4- and 4′-substituted, and naphthalene analogs,” Author's Abstract of Candidate's Dissertation, Khar'kov (1976), p. 24.Google Scholar
  4. 4.
    V. V. Danilov, A. S. Eremenko, Yu. T. Mazurenko, A. A. Rykov, Yu. L. Slominskii, and A. I. Stepanov, “Ketocyanines — a new class of generating compounds,” Kva'nt. Elektron., 4, No. 1, 195–198 (1977).Google Scholar
  5. 5.
    A. V. Aristov, V. V. Danilov, L. K. Denisov, M. B. Levin, V. N. Makarov, I. D. Radchenko, Yu. L. Slominskii, and A. S. Cherkasov, “Generation of ketocyanine dyes under lamp excitation conditions,” Opt. Spektrosk., 43, No. 5, 945–948 (1977).Google Scholar
  6. 6.
    J. Weinstein and G. M. Wyman, “A study of Β-amino-α,Β-unsaturated ketones,” J. Org. Chem., 23, No. 10, 1618–1622 (1958).Google Scholar
  7. 7.
    Yu. L. Slominskii and I. D. Radchenko, “Condensation of dimethine hemicyanines with ketones,” Khim. Geterotskii. Soed., No. 5, 711–712 (1974).Google Scholar
  8. 8.
    A. Weissberger (editor), Techniques of Organic Chemistry, Vol. 7, Organic Solvents, Wiley-Interscience (1955).Google Scholar
  9. 9.
    V. K. Lamer and H. C. Downes, “Indicator studies of acids and bases in benzene,” J. Am. Chem. Soc., 55, No. 5, 1840–1864 (1933).Google Scholar
  10. 10.
    A. K. Chibisov, “Investigation of the phototropic conversions of methyl red during pulse illumination,” Zh. Prikl. Spektroskop., 5, No. 5, 635–641 (1966).Google Scholar
  11. 11.
    A. K. Chibisov, “Photoisomerism of some dyes during pulse excitation,” Teor. Eksp. Khim., 2, No. 6, 825–829 (1966).Google Scholar
  12. 12.
    C. Wettermark, M. E. Langmuir, and D. G. Anderson, “Catalysis of the cis-trans isomerization of 2-hydroxy-5-methylazobenzene,” J. Am. Chem. Soc., 87, No. 3, 476–481 (1965).Google Scholar
  13. 13.
    K. Herbig, R. Huisgen, and H. Huber, “Cis-trans Isomerisierung bei Enamin-Β-Carbonestern, zum Sterischen Ablauf der Amin-Addition an Carbonester der Acetilenreihe,” Ber., 99, No. 8, 2546–2555 (1966).Google Scholar
  14. 14.
    J. Dobrowski and J. Terpinski, “Imine-enamine tautomerism. IX. Mechanisms of the cis-trans isomerization of enamino ketones,” Roczn. Chem., 41, No. 4, 697–706 (1967).Google Scholar
  15. 15.
    L. J. Andrews and R. M. Keefer, Molecular Complexes in Organic Chemistry, Holden-Day (1964).Google Scholar
  16. 16.
    Ya. F. Freimanis, Chemistry of Enaminoketones, Enaminoimines, and Enaminothiones [in Russian], Zinatne, Riga (1974).Google Scholar

Copyright information

© Plenum Publishing Corporation 1979

Authors and Affiliations

  • G. G. Dyadyusha
    • 1
  • A. A. Rykov
    • 1
  • Yu. L. Slominskii
    • 1
  1. 1.Institute of Organic ChemistryAcademy of Sciences of the Ukrainian SSRKiev

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