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BielawskiChristopher W

Bielawski, Christopher W.
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DC Field Value Language
dc.citation.endPage 7064 -
dc.citation.number 49 -
dc.citation.startPage 7061 -
dc.citation.title CHEMICAL COMMUNICATIONS -
dc.citation.volume 55 -
dc.contributor.author Kim, Youngsuk -
dc.contributor.author Bielawski, Christopher W. -
dc.contributor.author Lee, Eunsung -
dc.date.accessioned 2023-12-21T19:07:21Z -
dc.date.available 2023-12-21T19:07:21Z -
dc.date.created 2019-07-05 -
dc.date.issued 2019-06 -
dc.description.abstract Treating iminoxyl species with oxygen acceptors such as PPh3 resulted in oxygen atom transfer and afforded the corresponding iminyl radicals. DFT and other calculations revealed that association between the oxygen atom acceptors and the iminoxyl species results in the formation of key intermediates during the reaction. Subsequent dissociation is accompanied with homolytic cleavage of the N-O bond and generates iminyl radicals with spin densities that are localized on exocyclic nitrogen atoms. -
dc.identifier.bibliographicCitation CHEMICAL COMMUNICATIONS, v.55, no.49, pp.7061 - 7064 -
dc.identifier.doi 10.1039/c9cc03521d -
dc.identifier.issn 1359-7345 -
dc.identifier.scopusid 2-s2.0-85067235981 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/27250 -
dc.identifier.url https://pubs.rsc.org/en/content/articlelanding/2019/CC/C9CC03521D#!divAbstract -
dc.identifier.wosid 000471721700014 -
dc.language 영어 -
dc.publisher ROYAL SOC CHEMISTRY -
dc.title Oxygen atom transfer: a mild and efficient method for generating iminyl radicals -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Chemistry, Multidisciplinary -
dc.relation.journalResearchArea Chemistry -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus NITRIC-OXIDE -
dc.subject.keywordPlus CARBENES -
dc.subject.keywordPlus VALENCE -
dc.subject.keywordPlus CATION -
dc.subject.keywordPlus CHEMISTRY -

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