Synthesis and Characterization of g-Heteroaryl-substituted Pentamethine Cyanine Dyes with Carboxy or Methoxycarbonyl Substituents at the Two Heterocyclic End Groups, By Abdolmohammad Mehranpour

Research

Title	Synthesis and Characterization of g-Heteroaryl-substituted Pentamethine Cyanine Dyes with Carboxy or Methoxycarbonyl Substituents at the Two Heterocyclic End Groups
Type	Article
Keywords	—
Journal	JOURNAL OF HETEROCYCLIC CHEMISTRY
DOI	—
Researchers	Abdolmohammad Mehranpour (First researcher) , Sedigheh Hashemnia (Second researcher) ,

Abstract

Seven novel pentamethine cyanine dyes with 3,5-dimethylpyridinium-1-yl, pyridinium-1-yl, and 1-quinolinum-1-yl substituents in the g position of the methine chain containing ester or carboxylic acid groups in the ring of the dyes were synthesized via a three-step procedure. The visible spectral behavior of the pentamethine cyanine dyes was examined in DMSO. Elemental analysis, IR, 1H-NMR, 13C-NMR, and mass spectral (MS) data confirmed the molecular structure of the newly synthesized compounds.