Photoisomerization of two 2-hydroxy-5-arylazobenzaldehydes in solvents of different polarities.

Two azo dyes 2-hydroxy-5-(4-nitrophenylazo)benzaldehyde and 2-hydroxy-5-(4-chlorophenylazo)benzaldehyde dissolved in carbon tetrachloride, hexane, acetone and acetonitrile were irradiated with 365 nm UV light, and processes, occurring in them, were studied by NMR and UV-vis spectroscopy. It was established that reversible trans/cis photoisomerization of the molecules occurs in the non-polar solvents and is not observed in the polar solvents. 2D NOESY NMR spectroscopy was used to identify isomers of the azo compounds. Based on the chemical shifts of the signals, it was established that these compounds are in the trans-form before UV irradiation. Spectra of the azo dyes before and after UV irradiation allowed assignment of the chemical shifts of the cis-isomers. In polar solvents these compounds undergo a hypochromic effect under heating or irradiation with UV light. Both compounds exhibit solvatochromism. The shifts in NMR signals caused by photoisomerization of the molecules were compared with the shifts in the NMR signals of other azo compounds such as Disperse Orange 3, Disperse Red 1 and azobenzene.