Photochemical transformations of 1-arglcyanomethyl-9,10-anthraquinones Full article
Journal |
Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171 |
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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 | ||||
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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
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
Dates:
Published print: | Oct 1, 1995 |
Identifiers:
Web of science | WOS:A1995TQ44100026 |
Scopus | 2-s2.0-21844484866 |
Elibrary | 31114278 |
OpenAlex | W1966443648 |