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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(56812714700)*
dc.contributor.scopusid김영미(57207443602)*
dc.contributor.scopusid윤주영(7403587371)*
dc.date.modifydate20240301081003*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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