Premium
The Photofading of 1 –Arylazo–2–naphthols in Solution.
Author(s) -
Kuramoto Nobuhiro,
Kitao† Teijiro
Publication year - 1980
Publication title -
journal of the society of dyers and colourists
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.297
H-Index - 49
eISSN - 1478-4408
pISSN - 0037-9859
DOI - 10.1111/j.1478-4408.1980.tb03497.x
Subject(s) - chemistry , intramolecular force , tautomer , methanol , nitro , photochemistry , hydrazone , medicinal chemistry , substrate (aquarium) , singlet oxygen , acetone , singlet state , oxygen , stereochemistry , organic chemistry , alkyl , oceanography , geology , physics , nuclear physics , excited state
1–(Substituted phenylazo)–2–naphthols with a nitro group positioned para– or ortho– to the azo group, show anomalous photofading behaviour in methanol, i. e., their fastness to light is very much lower than that of similar compounds. On the other hand, although 1 –(o–nitrophenylazo)–2–naphthol (II) in alcoholic solvents faded to give similar products via photooxidative and/or photoreductive reactions, little photoreduction of the nitro group was detected, and the rate of photofading of II was lower than that of la. The contribution of intramolecular interaction, such as intramolecular bifurcated hydrogen bonding, involving the o–nitro group, azo group and o–hydroxy group of 1–(o–nitrophenylazo)–2–naphthol, are also discussed. Photochemical reaction of 1–(p–nitrophenylazo)–2–naphthol (la) in methanol, ethanol or 2–propanol produces not only oxidative but also reductive products, while photochemical reaction of la in acetone gives only oxidative products. From these results and earlier observations, it is suggested that the anomalous photofading of la is a substrate–specific phenomenon, and may be caused by photo–reduction of the nitro and azo groups to amino groups by the substrate, instead of the normal photo–oxidation of the hydrazone tautomer by singlet oxygen.