Pyrilocyanines. 36. α-Thienyl substituted pyrilo- and thiopyrilocyanines

Authors

  • М. А. Кудинова Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev 253660
  • B. В. Курдюков Institute of Organic Chemistry, National Academy of Sciences of Ukraine Kiev 253660
  • А. B. Качковский Institute of Organic Chemistry, National Academy of Sciences of Ukraine Kiev 253660
  • А. И. Толмачев Institute of Organic Chemistry, National Academy of Sciences of Ukraine Kiev 253660

Abstract

Symmetrical and nonsymmetrical 2,6- (and 4,6-)-di-α-thienyl substituted α- and γ-pyrilo- and thiopyrilocyanines have been synthesized. The effect of changing the phenyl groups for α-thienyl on the electronic absorption spectral parameters of the dyes obtained is discussed. It was found that such a change leads to a decrease in the effective length and increase in the electron donor ability of the hetero fragments containing these groups. The more intense coloring of the thienyl substituted dyes is due to interaction of the polymethine and quasilocal electronic transitions.

How to Cite
Kudinova, M. A.; Kurdyukov, V. V.; Kachkovskii, A. V.; Tolmachev, A. I. Chem. Heterocycl. Compd. 1998, 34, 438. [Khim. Geterotsikl. Soedin. 1998, 34, 494.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02290883

Published

1998-04-25

Issue

Section

Original Papers