Studies on UV/Vis Absorption Spectra of Azo Dyes. 24. The different effect of a 2‐methoxy and a 3‐methoxy group in 4‐N.N‐diethylaminoazobenzenes on colour
Heinz Mustroph, F. GUSSMANN
Abstract
Heinz Mustroph, F. GUSSMANN
Abstract
Abstract A number of 2‐ and 3‐methoxy‐substituted‐4‐N.N‐diethylaminoazobenzenes have been prepared and their absorption maxima in ethanol and toluene compared with the corresponding 4‐N.N‐diethylaminoazobenzenes. Both the 2‐ and 3‐methoxy groups cause a bathochromic shift, but the bathochromic shift of a 3‐methoxy group depends on the substituents in the diazo component. With increasing electron‐withdrawing strength of the substituents in the diazo component a progressive enhancement of bathochromic shift appears. In toluene all 3‐methoxy‐substituted dyes absorb at longer wavelengths compared with the 2‐methoxy‐substituted dyes.
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Abstract A number of 2‐ and 3‐methoxy‐substituted‐4‐N.N‐diethylaminoazobenzenes have been prepared and their absorption maxima in ethanol and toluene compared with the corresponding 4‐N.N‐diethylaminoazobenzenes. Both the 2‐ and 3‐methoxy groups cause a bathochromic shift, but the bathochromic shift of a 3‐methoxy group depends on the substituents in the diazo component. With increasing electron‐withdrawing strength of the substituents in the diazo component a progressive enhancement of bathochromic shift appears. In toluene all 3‐methoxy‐substituted dyes absorb at longer wavelengths compared with the 2‐methoxy‐substituted dyes.
Key concepts: Bathochromic shift, Toluene, Diazo, Chemistry, Photochemistry, Absorption (acoustics), Absorption spectroscopy, Hypsochromic shift