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dc.contributor.author윤주영*
dc.contributor.author김관묵*
dc.contributor.author권용억*
dc.date.accessioned2019-05-03T16:30:06Z-
dc.date.available2019-05-03T16:30:06Z-
dc.date.issued2019*
dc.identifier.issn0143-7208*
dc.identifier.otherOAK-24709*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/249713-
dc.description.abstractThe bis-binaphthol-pyrene derivative 1 (R isomer) and 2 (S isomer) selectively sense Zn2+ by undergoing a reversible fluorescent emission enhancement at 550 nm. Moreover, upon addition of Zn2+, the magnitude of the peak in the CD spectrum of 1 at 289 nm increases and the intensity of the peak at 272 nm decreases. Opposite changes were observed for 2 upon the addition Zn2+. The distinctive fluorescence and ratiometric CD spectral changes are attributed to a change in the dihedral angle between the binaphthol groups in 1 and 2 caused by Zn2+ binding. Probe 1 was further employed to image Zn2+ in cells. © 2019 Elsevier Ltd*
dc.languageEnglish*
dc.publisherElsevier Ltd*
dc.subjectBinapthol*
dc.subjectCircular dichroism*
dc.subjectFluorescent chemosensor for Zn2+*
dc.subjectFluorescent probe for Zn2+*
dc.subjectZn2+ imaging in cells*
dc.titleSelective fluorescent recognition of Zn2+ by using chiral binaphthol-pyrene probes*
dc.typeArticle*
dc.relation.volume167*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage29*
dc.relation.lastpage35*
dc.relation.journaltitleDyes and Pigments*
dc.identifier.doi10.1016/j.dyepig.2019.03.063*
dc.identifier.wosidWOS:000468712300005*
dc.identifier.scopusid2-s2.0-85064163975*
dc.author.googleShirbhate M.E.*
dc.author.googleJeong Y.*
dc.author.googleKo G.*
dc.author.googleBaek G.*
dc.author.googleKim G.*
dc.author.googleKwon Y.-U.*
dc.author.googleKim K.M.*
dc.author.googleYoon J.*
dc.contributor.scopusid윤주영(7403587371)*
dc.contributor.scopusid김관묵(35484385500)*
dc.contributor.scopusid권용억(7403459303)*
dc.date.modifydate20240118162450*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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