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Photochemical transformations of 1-arglcyanomethyl-9,10-anthraquinones Full article

Journal Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Output data Year: 1995, Volume: 44, Number: 10, Pages: 1907-1913 Pages count : 7 DOI: 10.1007/BF00707225
Tags photochemical transformations; 1-arylcyanomethyl-9,l0-anthraquinones; nucleophilic addition; oxidation; kinetics; quantum-chemical calculations
Authors Klimenko L.S. 1 , Mainagashev I.Ya. 1 , Leonenko Z.V. 2 , Gritsan N.P. 2
Affiliations
1 Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9 ul. Akad. Lavrent'eva, 630090, Novosibirsk, Russian Federation
2 Institute of Chemical Kinetics and Combustion Siberian Branch of the Russian Academy of Sciences, Novosibirsk State University, 3 ul. Institutskaya, 630090, Novosibirsk, Russian Federation

Abstract: Photochemical transformations of 1-arylcyanomethyl-9,10-anthraquinones were studied. it was established that under irradiation, the hydrogen atom of the substituted methyl group is transferred to a peri-quinoid oxygen atom to form the corresponding 9-hydroxy-1, 10-anthraquinone-1-arylcyanomethides, Dark transformations of photoinduced quinone-methides result from three competing parallel processes: intramolecular transfer of the hydrogen atom, a reaction with a solvent (alcohol), and oxidation by dissolved oxygen. The kinetics of these reactions were studied.
Cite: Klimenko L.S. , Mainagashev I.Y. , Leonenko Z.V. , Gritsan N.P.
Photochemical transformations of 1-arglcyanomethyl-9,10-anthraquinones
Russian Chemical Bulletin. 1995. V.44. N10. P.1907-1913. DOI: 10.1007/BF00707225 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Oct 1, 1995
Identifiers:
Web of science: WOS:A1995TQ44100026
Scopus: 2-s2.0-21844484866
Elibrary: 31114278
OpenAlex: W1966443648
Citing:
DB Citing
Web of science 5
Scopus 7
Elibrary 7
OpenAlex 1
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