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Kinetics and Mechanism of Anthracene Oxidation with tert-Butyl Hydroperoxide over Metal-Organic Frameworks Cr-MIL-101 and Cr-MIL-100 Full article

Journal Journal of Organometallic Chemistry
ISSN: 0022-328X
Output data Year: 2015, Volume: 793, Pages: 175-181 Pages count : 7 DOI: 10.1016/j.jorganchem.2015.03.022
Tags Anthracene, Kinetics, Mechanism, Metal-organic framework, Selective oxidation, tert-butyl hydroperoxide
Authors Ivanchikova I.D. 1 , Skobelev I.Y. 1 , Kholdeeva O.A. 1,2
Affiliations
1 Boreskov Institute of Catalysis, Pr. Ac. Lavrentieva 5, Novosibirsk 630090, Russia
2 Novosibirsk State University, Pirogova str. 2, Novosibirsk 630090, Russia

Funding (1)

1 Russian Foundation for Basic Research 13-03-00413

Abstract: The oxidation of anthracene (AN) with tert-butyl hydroperoxide (TBHP) over metal-organic frameworks (MOFs) Cr-MIL-101 and Cr-MIL-100 produced anthraquinone (AQ) in a nearly quantitative (>99%) yield after 1 and 4 h, respectively, at 100 °C in chlorobenzene (ClPh). At initial stages of the reaction, some amounts (<13%) of intermediate products, anthrahydroquinone and oxanthrone, were detected along with traces of 9-hydroxyanthracene and/or anthrone. Kinetic study revealed that the oxidation reaction is unaffected by the presence of molecular oxygen and is zero order in AN and first order in both TBHP and MOF catalyst. Additives of radical chain scavengers produced no effect on the reaction rate and selectivity. The activation energy Ea was found to be similar for MIL-101 and MIL-100 (15 kcal/mol) while pre-exponential factors were different (7·106 and 3·106 L/(mol·min), respectively). The kinetic results indicated that the AN oxidation with TBHP over both MIL-101 and MIL-100 is not controlled by diffusion. No adsorption of AN on the MOFs from ClPh solution was found at the reaction temperature. A mechanism that involves a reversible interaction between TBHP and CrIII centers within the MOF framework producing an active oxidizing species (rate-limiting step), followed by oxygen atom transfer from the peroxo species to the aromatic substrate to give primary oxygenated product(s), further oxidation of which leads to AQ, has been suggested.
Cite: Ivanchikova I.D. , Skobelev I.Y. , Kholdeeva O.A.
Kinetics and Mechanism of Anthracene Oxidation with tert-Butyl Hydroperoxide over Metal-Organic Frameworks Cr-MIL-101 and Cr-MIL-100
Journal of Organometallic Chemistry. 2015. V.793. P.175-181. DOI: 10.1016/j.jorganchem.2015.03.022 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Dec 17, 2014
Accepted: Mar 24, 2015
Published online: Apr 2, 2015
Published print: Sep 1, 2015
Identifiers:
Web of science: WOS:000360026000020
Scopus: 2-s2.0-84939569357
Elibrary: 24445043
Chemical Abstracts: 2015:619516
Chemical Abstracts (print): 163:282898
OpenAlex: W1969462375
Citing:
DB Citing
Web of science 10
Scopus 12
Elibrary 9
OpenAlex 14
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