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Anion effects on construction of Zn-II compounds with a chelating ligand bis(2-pyridylmethyl)amine and their catalytic activities

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dc.contributor.authorKim, Youngmee-
dc.contributor.authorPark, Byeong Kwon-
dc.contributor.authorEom, Geun Hee-
dc.contributor.authorKim, Soo Hyun-
dc.contributor.authorPark, Hyun Min-
dc.contributor.authorChoi, Young S.-
dc.contributor.authorJang, Ho G.-
dc.contributor.authorKim, Cheal-
dc.date.accessioned2021-09-07T15:58:44Z-
dc.date.available2021-09-07T15:58:44Z-
dc.date.created2021-06-14-
dc.date.issued2011-01-30-
dc.identifier.issn0020-1693-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/113245-
dc.description.abstractThree Zn-II complexes containing bispicam ligands (bispicam = bis(2-pyridylmethyl)amine), [Zn(bispicam)(2)](NO3)(2)center dot 2CH(3)OH 4A, [Zn(bispicam)(NO3)(2)] 4B, and [Zn(bispicam)(2)](OTf)(2) 6, were obtained, and their structures were determined by X-ray crystallography. Complexes of the general formulation [Zn(bispicam)(2)]X-2 (X = Cl (1), Br (2), I (3), NO3 (4A), ClO4 (5), and OTf (6)) show fac geometric isomers (a) or enantiomers (c) and (d) according to anions. Moreover, complexes 4-6 could carry out the catalytic transesterification of a range of esters with methanol under the mild conditions. Importantly, the catalyst 4B with an unsaturated structure has shown better efficiency than the catalysts, 4A, 5, and 6, having saturated structures. To explain this reactivity difference, two different reaction mechanisms have been proposed (metal-based vs. amide N-H-based). (C) 2010 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE SA-
dc.subjectN-HETEROCYCLIC CARBENES-
dc.subjectCOORDINATION POLYMERS-
dc.subjectCRYSTAL-STRUCTURES-
dc.subjectTRANSESTERIFICATION/ACYLATION REACTIONS-
dc.subject2,2&apos-
dc.subject-DIPYRIDYLAMINE HDPA-
dc.subjectZN(II) COMPOUNDS-
dc.subjectBUILDING-BLOCKS-
dc.subjectMETAL-
dc.subjectCOMPLEXES-
dc.subjectFRAMEWORKS-
dc.titleAnion effects on construction of Zn-II compounds with a chelating ligand bis(2-pyridylmethyl)amine and their catalytic activities-
dc.typeArticle-
dc.contributor.affiliatedAuthorJang, Ho G.-
dc.identifier.doi10.1016/j.ica.2010.11.029-
dc.identifier.scopusid2-s2.0-79251596466-
dc.identifier.wosid000285994200045-
dc.identifier.bibliographicCitationINORGANICA CHIMICA ACTA, v.366, no.1, pp.337 - 343-
dc.relation.isPartOfINORGANICA CHIMICA ACTA-
dc.citation.titleINORGANICA CHIMICA ACTA-
dc.citation.volume366-
dc.citation.number1-
dc.citation.startPage337-
dc.citation.endPage343-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Inorganic & Nuclear-
dc.subject.keywordPlusN-HETEROCYCLIC CARBENES-
dc.subject.keywordPlusCOORDINATION POLYMERS-
dc.subject.keywordPlusCRYSTAL-STRUCTURES-
dc.subject.keywordPlusTRANSESTERIFICATION/ACYLATION REACTIONS-
dc.subject.keywordPlus2,2&apos-
dc.subject.keywordPlus-DIPYRIDYLAMINE HDPA-
dc.subject.keywordPlusZN(II) COMPOUNDS-
dc.subject.keywordPlusBUILDING-BLOCKS-
dc.subject.keywordPlusMETAL-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusFRAMEWORKS-
dc.subject.keywordAuthorGeometric isomers-
dc.subject.keywordAuthorZinc(II) complexes-
dc.subject.keywordAuthorBis(2-pyridylmethyl)amine-
dc.subject.keywordAuthorTransesterification-
dc.subject.keywordAuthorCatalyst-
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