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dc.contributor.author김성진-
dc.contributor.author김영미-
dc.date.accessioned2016-08-28T12:08:53Z-
dc.date.available2016-08-28T12:08:53Z-
dc.date.issued2010-
dc.identifier.issn1359-7345-
dc.identifier.otherOAK-7051-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/221165-
dc.description.abstractmeso-Alkylidene (m-benzi)pentaphyrin containing exocyclic C=C double bonds at two meso-positions is synthesized and fully characterized for the first time. The single crystal X-ray crystallographic analysis shows a concave conformation with two pyrrole rings inverted. The first protonation occurs exclusively at core nitrogen. The synthesized compound displays concentration dependent chromogenic responses for fluoride anion in organic solvent. © The Royal Society of Chemistry 2010.-
dc.languageEnglish-
dc.titleMeso-Alkylidene (m-benzi)pentaphyrin: A modified pentaphyrin bearing exocyclic double bonds at meso-positions-
dc.typeArticle-
dc.relation.issue46-
dc.relation.volume46-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage8737-
dc.relation.lastpage8739-
dc.relation.journaltitleChemical Communications-
dc.identifier.doi10.1039/c0cc03263h-
dc.identifier.wosidWOS:000284229400009-
dc.identifier.scopusid2-s2.0-78549254876-
dc.author.googleJeong S.-D.-
dc.author.googleNowak-Krol A.-
dc.author.googleKim Y.-
dc.author.googleKim S.-J.-
dc.author.googleGryko D.T.-
dc.author.googleLee C.-H.-
dc.contributor.scopusid김성진(56812714700;34975057300)-
dc.contributor.scopusid김영미(8361744900;57207443602)-
dc.date.modifydate20220119153929-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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