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dc.contributor.author Kim, Bohee -
dc.contributor.author Jeong, Donghyun -
dc.contributor.author Cho, Jaeheung -
dc.date.available 2017-09-11T09:29:14Z -
dc.date.created 2017-09-11 -
dc.date.issued 2017-08 -
dc.identifier.issn 1359-7345 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/4462 -
dc.description.abstract Copper(ii)-alkylperoxo adducts, [Cu(CHDAP)(OOR)]+ (CHDAP = N,N′-dicyclohexyl-2,11-diaza[3,3](2,6)pyridinophane; R = C(CH3)2Ph and tBu), were prepared and characterized using various physicochemical methods. These are the first synthetic Cu(ii)-alkylperoxo complexes that can perform aldehyde deformylation (i.e., nucleophilic reactivity) under the stoichiometric reaction conditions, which was confirmed by kinetic studies. © 2017 The Royal Society of Chemistry. -
dc.language English -
dc.publisher Royal Society of Chemistry -
dc.title Nucleophilic reactivity of copper(II)-alkylperoxo complexes -
dc.type Article -
dc.identifier.doi 10.1039/c7cc03965d -
dc.identifier.scopusid 2-s2.0-85027550211 -
dc.identifier.bibliographicCitation Chemical Communications, v.53, no.67, pp.9328 - 9331 -
dc.description.isOpenAccess FALSE -
dc.subject.keywordPlus III-OOR COMPLEXES -
dc.subject.keywordPlus O BOND-CLEAVAGE -
dc.subject.keywordPlus HIGH-SPIN IRON(III)-ALKYLPEROXO -
dc.subject.keywordPlus NONHEME IRON MODELS -
dc.subject.keywordPlus SUPEROXIDE REDUCTASE -
dc.subject.keywordPlus ELECTRONIC-STRUCTURE -
dc.subject.keywordPlus COORDINATION SPHERE -
dc.subject.keywordPlus OXIDATION -
dc.subject.keywordPlus ACTIVATION -
dc.subject.keywordPlus MECHANISM -
dc.citation.endPage 9331 -
dc.citation.number 67 -
dc.citation.startPage 9328 -
dc.citation.title Chemical Communications -
dc.citation.volume 53 -
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Department of Physics and Chemistry Biomimetic Materials Laboratory 1. Journal Articles

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