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Synthesis of tetra- and pentacarbocyanine dyes with alkoxy groups in the β,β′ positions of the polymethine chain

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Chemistry of Heterocyclic Compounds Aims and scope

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Abstract

Previously unknown symmetrical and unsymmetrical β, β'-dialkoxytetracarbocyanine and β, β'-dialkoxypentacarbocyanine dyes have been synthesized by the condensation of β-alkoxy-substituted hexamethine and octamethine hemicyanines with quaternary salts of β-alkoxypropenyl derivatives of heterocyclic bases. Tetracarbocyanines with a symmetrical structure have also been obtained by the direct interaction of quaternary salts of β-alkoxypropenyl derivatives of heterocyclic bases with malonaldehyde dianil.

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References

  1. N. N. Sveshnikov, S. A. Kheifets, and N. S. Stokovskaya, USSR Authors' Certificate 109457; Byull. izobr., no. 4, 1958.

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Kheifets, S.A., Sveshnikov, N.N. Synthesis of tetra- and pentacarbocyanine dyes with alkoxy groups in the β,β′ positions of the polymethine chain. Chem Heterocycl Compd 3, 813–814 (1967). https://doi.org/10.1007/BF00474876

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  • DOI: https://doi.org/10.1007/BF00474876

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