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Synthesis and structure of penta-platinum sigma-bonded derivatives of corannulene

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dc.contributor.authorChoi, Hyunbong-
dc.contributor.authorKim, Chulwoo-
dc.contributor.authorPark, Ki-Min-
dc.contributor.authorKim, Jinho-
dc.contributor.authorKang, Youngjin-
dc.contributor.authorKo, Jaejung-
dc.date.accessioned2021-09-08T12:28:48Z-
dc.date.available2021-09-08T12:28:48Z-
dc.date.created2021-06-11-
dc.date.issued2009-10-15-
dc.identifier.issn0022-328X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/119111-
dc.description.abstractThe synthesis of a new class of Pt(II) complexes with corannulene by way of either oxidative addition or reductive coupling is reported and their crystal structures are investigated. The crystal structure for {trans-Pt(PEt3)(2)Cl}(4){cis-Pt(PEt3)(2)Cl}C20H5 (1) consists of two enantiomers in a unit cell and shows cis- and trans-configuration around Pt(II) due to bulky PEt3 ligands. The pentanuclear Pt(II) complex, 1, readily reacts with 1-ethynyl-4-nitrobenzene to afford the penta-alkynyl substituted Pt(II) complex (2). Although there are still bulky PEt3 ligands around the Pt atoms in 2, all five Pt(II) have trans-configurations. The bowl of corannulene in 2 is shallower than that of 1. Therefore, the bowl depth of corannulene plays a key role in the determination of molecular geometry of sigma-bonded pentanuclear complexes bearing corannulene. (C) 2009 Elsevier B. V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE SA-
dc.subjectNORMAL-COORDINATE CALCULATIONS-
dc.subjectPHASE MOLECULAR-STRUCTURE-
dc.subjectTO-BOWL INVERSION-
dc.subjectELECTRON-DIFFRACTION-
dc.subjectGEODESIC POLYARENE-
dc.subjectAB-INITIO-
dc.subjectBUCKYBOWL-
dc.subjectFULLERENES-
dc.subjectCOMPLEX-
dc.subjectBARRIER-
dc.titleSynthesis and structure of penta-platinum sigma-bonded derivatives of corannulene-
dc.typeArticle-
dc.contributor.affiliatedAuthorKo, Jaejung-
dc.identifier.doi10.1016/j.jorganchem.2009.07.015-
dc.identifier.scopusid2-s2.0-69949093625-
dc.identifier.wosid000269723700001-
dc.identifier.bibliographicCitationJOURNAL OF ORGANOMETALLIC CHEMISTRY, v.694, no.22, pp.3529 - 3532-
dc.relation.isPartOfJOURNAL OF ORGANOMETALLIC CHEMISTRY-
dc.citation.titleJOURNAL OF ORGANOMETALLIC CHEMISTRY-
dc.citation.volume694-
dc.citation.number22-
dc.citation.startPage3529-
dc.citation.endPage3532-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Inorganic & Nuclear-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusNORMAL-COORDINATE CALCULATIONS-
dc.subject.keywordPlusPHASE MOLECULAR-STRUCTURE-
dc.subject.keywordPlusTO-BOWL INVERSION-
dc.subject.keywordPlusELECTRON-DIFFRACTION-
dc.subject.keywordPlusGEODESIC POLYARENE-
dc.subject.keywordPlusAB-INITIO-
dc.subject.keywordPlusBUCKYBOWL-
dc.subject.keywordPlusFULLERENES-
dc.subject.keywordPlusCOMPLEX-
dc.subject.keywordPlusBARRIER-
dc.subject.keywordAuthorCorannulene-
dc.subject.keywordAuthorOxidative addition-
dc.subject.keywordAuthorX-ray structure-
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