Solvent effects on the UV-visible absorption spectra of some new 3-methyl-5-(Phenylamino)-4-((4-phenylazo-phenyl)azo)-2-substituted thiophene dyes

Abstract

The preparation of 3-methyl-5-(phenylamino)-4-((4-phenylazo-phenyl)azo)thiophene dyes 4a-d, having different polar groups at the second position, was described through hetero-cyclization of the precursor 4-mercapto-4-(phenylamino)-3-((4-phenylazo-phenyl)azo)but-3-en-2-one (3) with various α-chlorinated reagents. The absorption spectra of the synthesized thiophene dyes were studied in three solvents (MeOH, CHCl3, and DMF) to correlate the effect of solvent polarity as well as chemical structures on absorption in the UV–vis region. The absorption maximum (λmax) changed from 486 to 502 nm in methanol, from 502 to 512 nm in chloroform, and from 626 to 654 nm in DMF. The benzoyl group's introduction in the second position of the thiophene ring brings the absorption maxima to higher values (bathochromic shift).