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Cited 48 time in webofscience Cited 50 time in scopus
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dc.contributor.authorBr-
dc.contributor.authort, JR-
dc.contributor.authorLee, E-
dc.contributor.authorBoursalian, GB-
dc.contributor.authorRitter, T-
dc.date.accessioned2015-07-07T19:06:46Z-
dc.date.available2015-07-07T19:06:46Z-
dc.date.created2013-12-19-
dc.date.issued2014-01-
dc.identifier.issn2041-6520-
dc.identifier.other2015-OAK-0000028482en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/13100-
dc.description.abstractElectrophilic fluorinating reagents derived from fluoride are desirable for the synthesis of F-18-labeled molecules for positron emission tomography (PET). Here, we study the mechanism by which a Pd(IV)complex captures fluoride and subsequently transfers it to nucleophiles. The intermediate Pd(IV)-F is formed with high rates even at the nano-to micromolar fluoride concentrations typical for radiosyntheses with F-18 due to fast formation of an outer-sphere complex between fluoride and Pd(IV). The subsequent fluorine transfer from the Pd(IV)-F complex is proposed to proceed through an unusual SET/fluoride transfer/SET mechanism. The findings detailed in this manuscript provide a theoretical foundation suitable for addressing a more general approach for electrophilic fluorination with high specific activity F-18 PET imaging.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherThe Royal Society of Chemistry-
dc.relation.isPartOfCHEMICAL SCIENCE-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.subjectTRANSITION-METAL-COMPLEXES-
dc.subjectC-H FLUORINATION-
dc.subjectCATALYZED ALLYLIC FLUORINATION-
dc.subjectNUCLEAR MAGNETIC-RESONANCE-
dc.subjectLATE-STAGE FLUORINATION-
dc.subjectRADICAL CATIONS-
dc.subjectREDUCTIVE ELIMINATION-
dc.subjectSTILBENE DERIVATIVES-
dc.subjectXENON DIFLUORIDE-
dc.subjectNUCLEOPHILIC FLUORINATION-
dc.titleMechanism of electrophilic fluorination with Pd(IV): fluoride capture and subsequent oxidative fluoride transfer-
dc.typeArticle-
dc.contributor.college화학과en_US
dc.identifier.doi10.1039/C3SC52367E-
dc.author.googleBrandt J.R., Lee E., Boursalian G.B., Ritter T.en_US
dc.relation.volume5en_US
dc.relation.issue1en_US
dc.relation.startpage169en_US
dc.relation.lastpage179en_US
dc.contributor.id10145005en_US
dc.relation.journalCHEMICAL SCIENCEen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationCHEMICAL SCIENCE, v.5, no.1, pp.169 - 179-
dc.identifier.wosid000327601600020-
dc.date.tcdate2019-01-01-
dc.citation.endPage179-
dc.citation.number1-
dc.citation.startPage169-
dc.citation.titleCHEMICAL SCIENCE-
dc.citation.volume5-
dc.contributor.affiliatedAuthort, JR-
dc.identifier.scopusid2-s2.0-84888584215-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc28-
dc.description.scptc28*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusTRANSITION-METAL-COMPLEXES-
dc.subject.keywordPlusC-H FLUORINATION-
dc.subject.keywordPlusCATALYZED ALLYLIC FLUORINATION-
dc.subject.keywordPlusREDUCTIVE ELIMINATION-
dc.subject.keywordPlusRADICAL CATIONS-
dc.subject.keywordPlusMEDIATED FLUORINATION-
dc.subject.keywordPlusCHEMICAL-EXCHANGE-
dc.subject.keywordPlusION-
dc.subject.keywordPlusSELECTFLUOR-
dc.subject.keywordPlusF-18-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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