Abstract
The pathways of the thermal transformations of thiacarbocyanines with various alkyl groups attached to the ring nitrogen atoms of the heteroresidues, of 3,3′-diethylthiacarbocyanine with various anions, and its anhydro base were investigated. The results of the studies are compared with the results of quantumchemical calculations of the labilities of the bonds in these compounds by the Pariser-Parr-Pople method.
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