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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 Научная публикация

Журнал Journal of Organometallic Chemistry
ISSN: 0022-328X
Вых. Данные Год: 2015, Том: 793, Страницы: 175-181 Страниц : 7 DOI: 10.1016/j.jorganchem.2015.03.022
Ключевые слова Anthracene, Kinetics, Mechanism, Metal-organic framework, Selective oxidation, tert-butyl hydroperoxide
Авторы Ivanchikova I.D. 1 , Skobelev I.Y. 1 , Kholdeeva O.A. 1,2
Организации
1 Boreskov Institute of Catalysis, Pr. Ac. Lavrentieva 5, Novosibirsk 630090, Russia
2 Novosibirsk State University, Pirogova str. 2, Novosibirsk 630090, Russia

Информация о финансировании (1)

1 Российский фонд фундаментальных исследований 13-03-00413

Реферат: 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.
Библиографическая ссылка: 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 CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 17 дек. 2014 г.
Принята к публикации: 24 мар. 2015 г.
Опубликована online: 2 апр. 2015 г.
Опубликована в печати: 1 сент. 2015 г.
Идентификаторы БД:
Web of science: WOS:000360026000020
Scopus: 2-s2.0-84939569357
РИНЦ: 24445043
Chemical Abstracts: 2015:619516
Chemical Abstracts (print): 163:282898
OpenAlex: W1969462375
Цитирование в БД:
БД Цитирований
Web of science 10
Scopus 12
РИНЦ 9
OpenAlex 14
Альметрики: