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분자활성촉매반응연구단
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Ligand non-innocence allows isolation of a neutral and terminal niobium nitride

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dc.contributor.authorSenthil, Shuruthi-
dc.contributor.authorSeongyeon Kwon-
dc.contributor.authorHoyoung Im-
dc.contributor.authorGau, Michael R.-
dc.contributor.authorMu-Hyun Baik-
dc.contributor.authorMindiola, Daniel J.-
dc.date.accessioned2023-01-26T02:38:53Z-
dc.date.available2023-01-26T02:38:53Z-
dc.date.created2022-10-29-
dc.date.issued2022-10-
dc.identifier.issn1359-7345-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/12654-
dc.description.abstractComplex (PNP)NbCl2(N[(t)3u]Ar) (1) (PNP- = N [2-(PPr2)-Pr-i-4-methylphenyl](2); Ar = 3,5-Me2C6H3) reacts with one equiv. of NaN 3 to form a mixture of (PNPN)NbCl2(N[Bu-t]Ar) (2) and (PNP)Nb N(N[Bu-t]Ar) (3), both of which have been spectroscopically and crystallographically characterized, including N-15 isotopic labelling studies. Complex 3 represents the first structurally characterized example of a neutral and mononuclear Nb nitride. Independent studies established 3 to form via two-electron reduction of 2, whereas oxidation of 3 by two-electrons reversed the process. Computational studies suggest the transmetallation step to produce the intermediate [(PNP)NbCl2(N-3)(N[Bu-t]Ar)] (A) which extrudes N2 to form the phosphinimide [(PNP)NbCl2(N-3)(N[Bu-t]Ar)] (B) followed by disproportionation to 2 and low-valent [(PNP)Nb(N-3)(N[Bu-t]Ar)] (C). The latter then undergoes intramolecular N-atom transfer to form the nitride moiety in 3.-
dc.language영어-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleLigand non-innocence allows isolation of a neutral and terminal niobium nitride-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000863709400001-
dc.identifier.scopusid2-s2.0-85140312517-
dc.identifier.rimsid79176-
dc.contributor.affiliatedAuthorSeongyeon Kwon-
dc.contributor.affiliatedAuthorHoyoung Im-
dc.contributor.affiliatedAuthorMu-Hyun Baik-
dc.identifier.doi10.1039/d2cc04696b-
dc.identifier.bibliographicCitationCHEMICAL COMMUNICATIONS, v.58, no.84, pp.11795 - 11798-
dc.relation.isPartOfCHEMICAL COMMUNICATIONS-
dc.citation.titleCHEMICAL COMMUNICATIONS-
dc.citation.volume58-
dc.citation.number84-
dc.citation.startPage11795-
dc.citation.endPage11798-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusEFFECTIVE CORE POTENTIALS-
dc.subject.keywordPlusDINITROGEN CLEAVAGE-
dc.subject.keywordPlusMOLECULAR CALCULATIONS-
dc.subject.keywordPlusENERGY-
dc.subject.keywordPlusCONVERSION-
dc.subject.keywordPlusCOMPLEX-
dc.subject.keywordPlusREAGENT-
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > 1. Journal Papers (저널논문)
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