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Stoichiometric Reaction of Benzene with α-Form of Oxygen on FeZSM-5 Zeolites. Mechanism of Aromatics Hydroxylation by N2O Full article

Journal Journal of Molecular Catalysis (Continued after 1994 as Journal of Molecular Catalysis A: Chemical and Journal of Molecular Catalysis B: Enzymatic)
ISSN: 0304-5102
Output data Year: 1993, Volume: 84, Number: 1, Pages: 117-124 Pages count : 8 DOI: 10.1016/0304-5102(93)80090-H
Tags aromatics, benzene, FeZSM-5, hydroxylation, nitrous oxide, oxidation, surface oxygen, zeolites
Authors Sobolev V.I. 1 , Kharitonov A.S. 1 , Paukshtis Ye.A. 1 , Panov G.I. 1
Affiliations
1 Boreskov Institute of Catalysis

Abstract: A stoichiometric reaction of benzene with the surface α-oxygen produced in N2O decomposition has been studied over FeZSM-5 zeolites. Products of this reaction were extracted from the surface and analyzed by chromatography. The reaction has been shown to proceed readily at room temperature resulting in nearly quantitative yield of phenol. This explains the unique catalytic properties of FeZSM-5 zeolites and their ferrisilicate analogs in the hydroxylation of aromatics by N2O. A “monoatomic oxidation” mechanism is suggested to explain the fact of partial but not complete oxidation upon participation of highly active α-oxygen in the reaction.
Cite: Sobolev V.I. , Kharitonov A.S. , Paukshtis Y.A. , Panov G.I.
Stoichiometric Reaction of Benzene with α-Form of Oxygen on FeZSM-5 Zeolites. Mechanism of Aromatics Hydroxylation by N2O
Journal of Molecular Catalysis (Continued after 1994 as Journal of Molecular Catalysis A: Chemical and Journal of Molecular Catalysis B: Enzymatic). 1993. V.84. N1. P.117-124. DOI: 10.1016/0304-5102(93)80090-H WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Nov 13, 1992
Accepted: Apr 3, 1993
Published print: Sep 21, 1993
Published online: Oct 2, 2001
Identifiers:
Web of science: WOS:A1993LY01000015
Scopus: 2-s2.0-0027663802
Elibrary: 31578916
Chemical Abstracts: 1994:54032
Chemical Abstracts (print): 120:54032
OpenAlex: W2017663036
Citing:
DB Citing
Web of science 96
Scopus 106
Elibrary 111
OpenAlex 105
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