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dc.contributor.author윤주영*
dc.date.accessioned2016-08-28T12:08:53Z-
dc.date.available2016-08-28T12:08:53Z-
dc.date.issued2010*
dc.identifier.issn0040-4020*
dc.identifier.otherOAK-6324*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/220578-
dc.description.abstractTwo 4,5-disubstituted-1,8-naphthalimide derivatives 1 and 2 were synthesized as ratiometric fluorescent and colorimetric sensors for Cu2+, respectively. In 100% aqueous solutions of 1, the presence of Cu2+ induces a strong and increasing fluorescent emission centered at 478 nm at the expense of the fluorescent emission of 1 centered at 534 nm. Compound 2 senses Cu2+ by means of a colorimetric (primrose yellow to pink) method with a thorough quench in emission attributed to the deprotonation of the secondary amine conjugated to the naphthalimide fluorophore. 1-Cu2+ and 2-Cu2+ sense cyanide in ratiometric way via colorimetric and fluorescent changes. © 2010 Elsevier Ltd. All rights reserved.*
dc.languageEnglish*
dc.titleRatiometric fluorescent and colorimetric sensors for Cu2+ based on 4,5-disubstituted-1,8-naphthalimide and sensing cyanide via Cu2+ displacement approach*
dc.typeArticle*
dc.relation.issue9*
dc.relation.volume66*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage1678*
dc.relation.lastpage1683*
dc.relation.journaltitleTetrahedron*
dc.identifier.doi10.1016/j.tet.2010.01.008*
dc.identifier.wosidWOS:000274984800008*
dc.identifier.scopusid2-s2.0-75149117765*
dc.author.googleXu Z.*
dc.author.googlePan J.*
dc.author.googleSpring D.R.*
dc.author.googleCui J.*
dc.author.googleYoon J.*
dc.contributor.scopusid윤주영(7403587371)*
dc.date.modifydate20240118162450*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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