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dc.contributor.author김성진-
dc.contributor.author김영미-
dc.contributor.author윤주영-
dc.contributor.authorK.M.K.Swamy-
dc.date.accessioned2016-08-28T10:08:24Z-
dc.date.available2016-08-28T10:08:24Z-
dc.date.issued2013-
dc.identifier.issn0143-7208-
dc.identifier.otherOAK-10382-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/223975-
dc.description.abstractRhodamine derivatives bearing the thiophene (1) and bisthiophene (2) groups are synthesized and their binding selectivity toward various metal ions was studied. The X-ray crystal structure of 1 was also reported. Probes 1 and 2 showed highly selective "Off-On" fluorescence changes with Hg 2+ among various metal ions. These selective changes were attributed to the spirolactam ring opening processes and subsequent hydrolysis. Probes 1 and 2 were sucessfully applied to the cell-imaging of Hg2+ using HeLa cells. © 2013 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.titleRhodamine hydrazone derivatives bearing thiophene group as fluorescent chemosensors for Hg2+-
dc.typeArticle-
dc.relation.issue2-
dc.relation.volume99-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage323-
dc.relation.lastpage328-
dc.relation.journaltitleDyes and Pigments-
dc.identifier.doi10.1016/j.dyepig.2013.05.015-
dc.identifier.wosidWOS:000323095000009-
dc.identifier.scopusid2-s2.0-84879487940-
dc.author.googlePark S.-
dc.author.googleKim W.-
dc.author.googleSwamy K.M.K.-
dc.author.googleLee H.Y.-
dc.author.googleJung J.Y.-
dc.author.googleKim G.-
dc.author.googleKim Y.-
dc.author.googleKim S.-J.-
dc.author.googleYoon J.-
dc.contributor.scopusid김성진(34975057300)-
dc.contributor.scopusid김영미(8361744900)-
dc.contributor.scopusid윤주영(7403587371)-
dc.date.modifydate20201102081004-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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