DSpace at EWHA: Hydrogen atom abstraction and hydride transfer reactions by iron(IV)-oxo porphyrins

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DSpace at EWHA자연과학대학 화학·나노과학전공 Journal papers

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DC Field	Value	Language
dc.contributor.author	남원우	*
dc.contributor.author	Shunichi Fukuzumi	*
dc.contributor.author	이용민	*
dc.date.accessioned	2016-08-28T12:08:03Z	-
dc.date.available	2016-08-28T12:08:03Z	-
dc.date.issued	2008	*
dc.identifier.issn	1433-7851	*
dc.identifier.other	OAK-5072	*
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/220065	-
dc.description.abstract	(Chemical Equation Presented) True identity revealed: The C-H bond activation of alkyl aromatics by synthetic iron(IV)-oxo porphyrin species and the hydride transfer of NADH analogues to them occur through H-atom abstraction and proton-coupled electron-transfer mechanisms, respectively. Mechanistic studies revealed that iron(IV)-oxo porphyrin π, not iron(IV)-oxo porphyrin pradical cations, are the true oxidant. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.	*
dc.language	English	*
dc.title	Hydrogen atom abstraction and hydride transfer reactions by iron(IV)-oxo porphyrins	*
dc.type	Article	*
dc.relation.issue	38	*
dc.relation.volume	47	*
dc.relation.index	SCI	*
dc.relation.index	SCIE	*
dc.relation.index	SCOPUS	*
dc.relation.startpage	7321	*
dc.relation.lastpage	7324	*
dc.relation.journaltitle	Angewandte Chemie - International Edition	*
dc.identifier.doi	10.1002/anie.200802346	*
dc.identifier.wosid	WOS:000259382900035	*
dc.identifier.scopusid	2-s2.0-53249136446	*
dc.author.google	Jeong Y.J.	*
dc.author.google	Kang Y.	*
dc.author.google	Han A.-R.	*
dc.author.google	Lee Y.-M.	*
dc.author.google	Kotani H.	*
dc.author.google	Fukuzumi S.	*
dc.author.google	Nam W.	*
dc.contributor.scopusid	남원우(7006569723)	*
dc.contributor.scopusid	Shunichi Fukuzumi(35430038100;58409757400)	*
dc.contributor.scopusid	이용민(36546331100;35233855500;57192113229)	*
dc.date.modifydate	20240401081001	*