Abstract
Asymmetric carbocyanine dyes, the solutions of which are characterized by the presence of several absorption bands in the visible and near-IR regions, were synthesized from 4,5-dimethyl-1-oxo-2-phenyl-1,5-dihydrothiazolo[3,2-a]quinoxalin-3-ium perchlorate. Their deep color is due both to a more effective length of the condensed heterocyclic system and to the strong interaction of the electronic transitions, localized on the polymethine chain and on the heterocyclic ring.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1113–1116, August, 1992.
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Fedotov, K.V. Asymmetric polymethine dyes based on thiazolo[3,2-a]quinoxalinium salts. Chem Heterocycl Compd 28, 937–940 (1992). https://doi.org/10.1007/BF00531331
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DOI: https://doi.org/10.1007/BF00531331