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dc.contributor.author남원우*
dc.date.accessioned2016-08-28T12:08:44Z-
dc.date.available2016-08-28T12:08:44Z-
dc.date.issued2007*
dc.identifier.issn0001-4842*
dc.identifier.otherOAK-4138*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/219879-
dc.description.abstractHigh-valent iron(IV)-oxo species have been implicated as the key reactive intermediates in the catalytic cycles of dioxygen activation by heme and non-heme iron enzymes. Our understanding of the enzymatic reactions has improved greatly via investigation of spectroscopic and chemical properties of heme and non-heme iron(IV)-oxo complexes. In this Account, reactivities of synthetic iron(IV)-oxo porphyrin π-cation radicals and mononuclear non-heme iron(IV)-oxo complexes in oxygenation reactions have been discussed as chemical models of cytochrome P450 and non-heme iron enzymes. These results demonstrate how mechanistic developments in biomimetic research can help our understanding of dioxygen activation and oxygen atom transfer reactions in nature. © 2007 American Chemical Society.*
dc.languageEnglish*
dc.titleHigh-valent iron(IV)-oxo complexes of heme and non-heme ligands in oxygenation reactions*
dc.typeConference Paper*
dc.relation.issue7*
dc.relation.volume40*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage522*
dc.relation.lastpage531*
dc.relation.journaltitleAccounts of Chemical Research*
dc.identifier.doi10.1021/ar700027f*
dc.identifier.wosidWOS:000248074000008*
dc.identifier.scopusid2-s2.0-34547728317*
dc.author.googleNam W.*
dc.contributor.scopusid남원우(7006569723)*
dc.date.modifydate20240116111857*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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