EPR Detection of Fe(V)=O Active Species in Nonheme Iron-Catalyzed Oxidations | Sciact

EPR Detection of Fe(V)=O Active Species in Nonheme Iron-Catalyzed Oxidations Научная публикация

Журнал

Catalysis Communications
ISSN: 1566-7367

Вых. Данные

Год: 2012, Том: 29, Страницы: 105-108 Страниц : 4 DOI: 10.1016/j.catcom.2012.09.029

Авторы

Lyakin Oleg Y. ^1,2 , Prat Irene ³ , Bryliakov Konstantin P. ^1,2 , Costas Miguel ³ , Talsi Evgenii P. ^1,2

Организации

1	Siberian Branch of the Russian Academy of Sciences, Boreskov Institute of Catalysis, Pr. Lavrentieva 5, Novosibirsk 630090, Russian Federation
2	Novosibirsk State University, Ul. Pirogova 2, Novosibirsk 630090, Russian Federation
3	Institut de Química Computacional i Departament de Química, Universitat de Girona, Campus de Montilivi, Girona 17071, Spain

Very recently, in situ cryospray-assisted variable temperature mass spectrometry (VT-MS) has been used to obtain the first convincing evidence for a HO–FeV=O intermediate in the catalyst system [(Me2PyTACN) FeII(OTf)2] (4)/H2O2 (Me2PyTACN=1-(2′-pyridylmethyl)-4,7-dimethyl-1,4,7-triazacyclononane, OTf=OSO2CF3). The herein presented EPR spectroscopic study of the same system witnesses the formation of S=1/2 reactive iron species. Its EPR parameters, in combination with its reactivity pattern toward cyclohexene and with independently obtained VT-MS data, allow for its reasonable assignment to the reactive [(Me2PyTACN)FeV=O(OH)]2+ (4c) species

Lyakin O.Y. , Prat I. , Bryliakov K.P. , Costas M. , Talsi E.P.
EPR Detection of Fe(V)=O Active Species in Nonheme Iron-Catalyzed Oxidations
Catalysis Communications. 2012. V.29. P.105-108. DOI: 10.1016/j.catcom.2012.09.029 WOS Scopus РИНЦ CAPlusCA OpenAlex Sciact

Поступила в редакцию:	20 июл. 2012 г.
Принята к публикации:	25 сент. 2012 г.
Опубликована online:	2 окт. 2012 г.
Опубликована в печати:	1 дек. 2012 г.

Web of science:	WOS:000313024300022
Scopus:	2-s2.0-84867623300
РИНЦ:	20496595
Chemical Abstracts:	2012:1708067
Chemical Abstracts (print):	158:76745
OpenAlex:	W2087366412
Sciact:	575

БД	Цитирований
Scopus	40
OpenAlex	40