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PHOTOLYSIS OF 1,2-ANTHRAQUINONE DIAZIDE IN AROMATIC-HYDROCARBONS Full article

Journal BULLETIN OF THE RUSSIAN ACADEMY OF SCIENCES-DIVISION OF CHEMICAL SCIENCE
ISSN: 1063-5211
Output data Year: 1992, Volume: 41, Number: 4, Pages: 789-791 Pages count : 3 DOI: 10.1007/BF01150908
Tags PHOTOLYSIS; 1,2-ANTHRAQUINONE DIAZIDE; AROMATIC HYDROCARBONS; ISOMERS
Authors Klimenko L.S. 1 , Mainagashev I.Ya. 1 , Fokin E.P. 1
Affiliations
1 Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk 630090

Abstract: It has been determined that the main products of photolysis of 1,2-anthraquinone diazide in benzene, toluene, anisole, nitrobenzene, and pyridine are the corresponding 1-hydroxy-2-arylanthraquinones that form as a mixture of ortho, meta, and para isomers with significant content of the meta isomer (40-55%).
Cite: Klimenko L.S. , Mainagashev I.Y. , Fokin E.P.
PHOTOLYSIS OF 1,2-ANTHRAQUINONE DIAZIDE IN AROMATIC-HYDROCARBONS
BULLETIN OF THE RUSSIAN ACADEMY OF SCIENCES-DIVISION OF CHEMICAL SCIENCE. 1992. V.41. N4. P.789-791. DOI: 10.1007/BF01150908 WOS Scopus OpenAlex
Dates:
Published print: Apr 1, 1992
Identifiers:
Web of science: WOS:A1992KB91200014
Scopus: 2-s2.0-34249838627
OpenAlex: W2953148498
Citing:
DB Citing
Web of science 1
Scopus 1
OpenAlex 2
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