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dc.contributor.author김성진*
dc.contributor.author김영미*
dc.date.accessioned2016-08-28T12:08:49Z-
dc.date.available2016-08-28T12:08:49Z-
dc.date.issued2011*
dc.identifier.issn0277-5387*
dc.identifier.otherOAK-7684*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/221711-
dc.description.abstractSix new structures of ZnII complexes containing 2,2′-bipyridine (2,2′-bpy) ligands have been determined. Halide anions were used as simple coordinating ligands to form a tetrahedral environment around the ZnII ion. Nitrate and benzoate anions were used as chelating ligands to form an octahedral environment. For non-coordinating ClO4- and bridging SO42- anions, three 2,2′-bpy ligands chelate ZnII to form an octahedral environment, and both ClO4- and SO42- anions occupy empty positions between the metal cations for charge balance. Polymeric structures of the ZnII-2,2′-bpy complexes are produced by hydrogen bonding. [Zn(2,2′-bpy)(O2CC 6H5)2] catalyzed efficiently the transesterification reaction of esters with methanol under the neutral conditions, while the remaining compounds showed very slow conversions. © 2011 Elsevier Ltd. All rights reserved.*
dc.languageEnglish*
dc.titleAnion effects on the crystal structures of ZnII complexes containing 2,2′-bipyridine: Their photoluminescence and catalytic activities*
dc.typeArticle*
dc.relation.issue9*
dc.relation.volume30*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage1555*
dc.relation.lastpage1564*
dc.relation.journaltitlePolyhedron*
dc.identifier.doi10.1016/j.poly.2011.03.040*
dc.identifier.wosidWOS:000291498600016*
dc.identifier.scopusid2-s2.0-79955760673*
dc.author.googleEom G.H.*
dc.author.googlePark H.M.*
dc.author.googleHyun M.Y.*
dc.author.googleJang S.P.*
dc.author.googleKim C.*
dc.author.googleLee J.H.*
dc.author.googleLee S.J.*
dc.author.googleKim S.-J.*
dc.author.googleKim Y.*
dc.contributor.scopusid김성진(56812714700)*
dc.contributor.scopusid김영미(57207443602)*
dc.date.modifydate20240301081003*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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