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The study of photoisomerisation of 1-aryloxyanthraquinones by NMR spectroscopy and UV spectrophotometry
Authors:S P Babailov  L S Klimenko  I Ya Mainagashev
Institution:(1) A. V. Nikolaev Institute of Inorganic Chemistry, Siberian Division, Russian Academy of Sciences, Novosibirsk;(2) Institute of Organic Chemistry, Siberian Division, Russian Academy of Sciences, Novosibirsk;(3) Institute of Chemical Biology and Fundamental Medicine, Siberian Division, Russian Academy of Sciences, Novosibirsk
Abstract:It has been stated by 1H NMR and UV spectrophotometry that 1-(4-tert-butil-phenoxy)-2-cetylamino-9,10-anthraquinone photoisomerizes to 9-(4-tert-butylphenoxy)-2-cetylamino-1,10-anthraquinon with quantum yield ? = 0.4 ±0.1 under light excitation in the absorption band region in the UV/visible spectrum range with the maximum λ = 441 nm.
Keywords:NMR  photoisomerization  1-aryloxyanthraquinones  photochemistry  UV spectrophotometry  anthraquinones  photo-induced molecular dynamics
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