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Azomethine and merocyanine dyes based on 3-arylbenzo[f]quinolinium salts and their spectral and electrophotographic properties

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Azomethine dyes were obtained by reaction of 1-methyl- and 1,2-dimethyl-3-arylbenzo[f]quinolinium methiodides with 1-nitroso-2-naphthol. Merocyanine dyes were isolated by the action of KOH on 2-hydroxy-5,6-benzostyryl derivatives of 3-arylbenzo[f]quinolinium salts. The absorption spectra of the dyes in ethanol and chloroform are presented, and it is shown that, as compared with the spectra of the merocyanines, there is a bathochromic shift of the absorption bands in the spectra of the azomethine dyes. The azomethine and merocyanine dyes have solvatochromic properties and display photosensitivity in the UV and visible regions when they are introduced into a polymer matrix.

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Authors and Affiliations

  1. Institute of Physical Organic Chemistry, Academy of Sciences of the Belorussian SSR, 220603, Minsk

    N. S. Kozlov, O. D. Zhikhareva, L. N. Fedorova, T. D. Butmerchuk & R. N. Kuz'min

  2. T. G. Shevchenko Kiev State University, 252017, Kiev

    N. S. Kozlov, O. D. Zhikhareva, L. N. Fedorova, T. D. Butmerchuk & R. N. Kuz'min

Authors
  1. N. S. Kozlov
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  2. O. D. Zhikhareva
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  3. L. N. Fedorova
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  4. T. D. Butmerchuk
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  5. R. N. Kuz'min
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1343–1347, October, 1977.

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Kozlov, N.S., Zhikhareva, O.D., Fedorova, L.N. et al. Azomethine and merocyanine dyes based on 3-arylbenzo[f]quinolinium salts and their spectral and electrophotographic properties. Chem Heterocycl Compd 13, 1075–1079 (1977). https://doi.org/10.1007/BF00480140

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  • DOI: https://doi.org/10.1007/BF00480140

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