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dc.contributor.authorShin, JY-
dc.contributor.authorHepperle, SS-
dc.contributor.authorDolphin, D-
dc.date.accessioned2018-10-04T06:25:25Z-
dc.date.available2018-10-04T06:25:25Z-
dc.date.created2011-03-17-
dc.date.issued2009-12-09-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/92483-
dc.description.abstractA meso-2,6-dichlorophenyl pentapyrrin was prepared using a modified method for dipyrrane synthesis followed by simple DDQ oxidation. The fully conjugated structures formed via redox inter-conversions were studied using crystallographic as well as observed and calculated spectral data. (C) 2009 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPerganmon-Elsevier Science LTD-
dc.relation.isPartOfTetrahedron Letters-
dc.titleLinear Fully Conjugated meso-Aryl Pentapyrrins-
dc.typeArticle-
dc.identifier.doi10.1016/j.tetlet.2009.09.145-
dc.type.rimsART-
dc.identifier.bibliographicCitationTetrahedron Letters, v.50, no.49, pp.6909 - 6912-
dc.identifier.wosid000271603000047-
dc.date.tcdate2019-02-01-
dc.citation.endPage6912-
dc.citation.number49-
dc.citation.startPage6909-
dc.citation.titleTetrahedron Letters-
dc.citation.volume50-
dc.contributor.affiliatedAuthorShin, JY-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc4-
dc.type.docTypeArticle-
dc.subject.keywordPlusMOLECULAR-ORBITAL METHODS-
dc.subject.keywordPlusDENSITY-FUNCTIONAL THEORY-
dc.subject.keywordPlusIMPLEMENTATION-
dc.subject.keywordPlusPORPHYRINS-
dc.subject.keywordPlusSOLUTES-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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