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5-Hetaryl-substituted 2-methyleneindolines and polymethine dyes based on them

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

2-Methyleneindolines containing benzazole residues at the 5-position were synthesized and polymethine dyes were obtained from them. The bathochromic shifts induced by the introduction of heterocyclic residues into indocyanines exceed the similar shifts induced by the same heterocycles in thio and quinocyanines.

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Authors and Affiliations

  1. Institute of Organic Chemistry, Academy of Sciences of the Ukrainian SSR, 252660, Kiev

    A. A. Tolmachev, L. N. Babichenko, V. S. Tolmacheva, T. S. Chmilenko & A. K. Sheinkman

  2. Dnepropetrovsk Construction Engineering Institute, 320660, Dnepropetrovsk

    A. A. Tolmachev, L. N. Babichenko, V. S. Tolmacheva, T. S. Chmilenko & A. K. Sheinkman

Authors
  1. A. A. Tolmachev
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  2. L. N. Babichenko
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  3. V. S. Tolmacheva
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  4. T. S. Chmilenko
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  5. A. K. Sheinkman
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1050–1054, August, 1990.

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Tolmachev, A.A., Babichenko, L.N., Tolmacheva, V.S. et al. 5-Hetaryl-substituted 2-methyleneindolines and polymethine dyes based on them. Chem Heterocycl Compd 26, 877–880 (1990). https://doi.org/10.1007/BF00480860

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  • DOI: https://doi.org/10.1007/BF00480860

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