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Selective oxidation of aromatic compounds on zeolites using N2O as a mild oxidant Full article

Journal Catalysis Today
ISSN: 0920-5861 , E-ISSN: 1873-4308
Output data Year: 2000, Volume: 61, Number: 1-4, Pages: 123-128 Pages count : 6 DOI: 10.1016/s0920-5861(00)00354-0
Authors Kustov L.M 1 , Tarasov A.L 1 , Bogdan V.I 1 , Tyrlov A.A 1 , Fulmer J.W 2
Affiliations
1 N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, 117913 Russia
2 General Electric Company, GE Plastics, 1 Lexan Lane, Mt. Vernon, IN 47620, USA

Abstract: Dehydroxylated ZSM-5 type zeolites are used for selective oxidation of aromatic compounds, including benzene, chlorobenzene, styrene, difluorobenzenes, phenol, alkylbenzenes into corresponding phenols and diphenols using nitrous oxide as a mild oxidant. In the case of benzene, the yield of phenol reaches 70–80%. Extremely high selectivity (∼98–100%) in the case of benzene and ∼85% in the case of difluorobenzenes and high regioselectivities are observed on the dehydroxylated HZSM-5 zeolite. The active sites are shown to be the strong Lewis acid–base pair sites formed upon dehydroxylation of the zeolites. The reaction mechanism that is alternative to the proposed iron-mediated mechanism is discussed.
Cite: Kustov L.M. , Tarasov A.L. , Bogdan V.I. , Tyrlov A.A. , Fulmer J.W.
Selective oxidation of aromatic compounds on zeolites using N2O as a mild oxidant
Catalysis Today. 2000. V.61. N1-4. P.123-128. DOI: 10.1016/s0920-5861(00)00354-0 WOS Scopus OpenAlex
Identifiers:
≡ Web of science: WOS:000089455900017
≡ Scopus: 2-s2.0-0034251505
≡ OpenAlex: W1574860761
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