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Cited 9 time in webofscience Cited 9 time in scopus
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dc.contributor.authorKim, WB-
dc.contributor.authorPark, KH-
dc.contributor.authorLee, JS-
dc.date.accessioned2016-03-31T13:04:20Z-
dc.date.available2016-03-31T13:04:20Z-
dc.date.created2009-02-28-
dc.date.issued2002-06-17-
dc.identifier.issn1381-1169-
dc.identifier.other2002-OAK-0000002750-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/19006-
dc.description.abstractA coupled oxidative carbonylation of bisphenol-A and phenol was investigated using a redox catalytic system of palladium acetate and cerium acetate as a novel scheme for a direct synthesis of phenylcarbotiate-ended polycarbonate precursors amenable to polycondensation in a current phosgene-free polycarbonate process. Reaction variables such as solvents, bases and organic co-catalysts were examined in our novel scheme. Removal of water co-produced with desired products and adjustment of the reactants molar ratio of phenol to bisphenol-A appeared to be most critical for highly selective formation of the desired phenylcarbonate-ended precursors in one-step. (C) 2002 Elsevier Science B.V. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.relation.isPartOfJOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL-
dc.subjectpolycarbonate precursor-
dc.subjectphosgene-free synthesis-
dc.subjectcoupled carbonylation-
dc.subjectbisphenol-A-
dc.subjectphenol-
dc.subjectPd-Ce redox catalyst-
dc.subjectGAS-PHASE TRANSESTERIFICATION-
dc.subjectDIPHENYL CARBONATE-
dc.subjectDIMETHYL CARBONATE-
dc.subjectSYSTEM-
dc.subjectDIMETHYLCARBONATE-
dc.subjectMONOXIDE-
dc.subjectCO-
dc.titleCoupled oxidative carbonylation of bisphenol-A and phenol into phenylcarbonate-ended polycarbonate precursors over a homogeneous Pd-Ce redox catalyst-
dc.typeArticle-
dc.contributor.college화학공학과-
dc.identifier.doi10.1016/S1381-1169(02)00011-0-
dc.author.googleKim, WB-
dc.author.googlePark, KH-
dc.author.googleLee, JS-
dc.relation.volume184-
dc.relation.issue1-2-
dc.relation.startpage39-
dc.relation.lastpage49-
dc.contributor.id10087281-
dc.relation.journalJOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, v.184, no.1-2, pp.39 - 49-
dc.identifier.wosid000176634000005-
dc.date.tcdate2019-01-01-
dc.citation.endPage49-
dc.citation.number1-2-
dc.citation.startPage39-
dc.citation.titleJOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL-
dc.citation.volume184-
dc.contributor.affiliatedAuthorLee, JS-
dc.identifier.scopusid2-s2.0-0037124938-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc8-
dc.type.docTypeArticle-
dc.subject.keywordPlusGAS-PHASE TRANSESTERIFICATION-
dc.subject.keywordPlusDIPHENYL CARBONATE-
dc.subject.keywordPlusDIMETHYL CARBONATE-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusDIMETHYLCARBONATE-
dc.subject.keywordPlusMONOXIDE-
dc.subject.keywordPlusCO-
dc.subject.keywordAuthorpolycarbonate precursor-
dc.subject.keywordAuthorphosgene-free synthesis-
dc.subject.keywordAuthorcoupled carbonylation-
dc.subject.keywordAuthorbisphenol-A-
dc.subject.keywordAuthorphenol-
dc.subject.keywordAuthorPd-Ce redox catalyst-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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