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Coumarin-Derived Cu2+-Selective Fluorescence Sensor: Synthesis, Mechanisms, and Applications in Living Cells

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dc.contributor.authorJung, Hyo Sung-
dc.contributor.authorKwon, Pil Seung-
dc.contributor.authorLee, Jeong Won-
dc.contributor.authorKim, Jae Il-
dc.contributor.authorHong, Chang Seop-
dc.contributor.authorKim, Jong Wan-
dc.contributor.authorYan, Shihai-
dc.contributor.authorLee, Jin Yong-
dc.contributor.authorLee, Jung Hwa-
dc.contributor.authorJoo, Taiha-
dc.contributor.authorKim, Jong Seung-
dc.date.accessioned2021-09-08T19:39:52Z-
dc.date.available2021-09-08T19:39:52Z-
dc.date.created2021-06-19-
dc.date.issued2009-02-11-
dc.identifier.issn0002-7863-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/120579-
dc.description.abstractA novel coumarin-based fluorogenic probe bearing the 2-picolyl unit (1) was developed as a fluorescent chemosensor with high selectivity and suitable affinity in biological systems toward Cu2+ over other cations tested. The fluorescence on-off mechanism was studied by femtosecond time-resolved fluorescence (TRF) upconversion technique and ab initio calculations. The receptor can be applied to the monitoring of Cu2+ ion in aqueous solution with a pH span 4-10. To confirm the suitability of 1 for biological applications, we also employed it for the fluorescence detection of the changes of intracellular Cu2+ in cultured cells. The results indicate that 1 should be useful for the fluorescence microscopic imaging and the study on the biological functions Of Cu2+..-
dc.languageEnglish-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.subjectFLUORIDE-SELECTIVE FLUORESCENT-
dc.subjectHYDROGEN-PEROXIDE-
dc.subjectCU-II-
dc.subjectCOPPER-
dc.subjectION-
dc.subjectCHEMOSENSOR-
dc.subjectFLUOROIONOPHORE-
dc.subjectCOMPLEXES-
dc.subjectZINC-
dc.subjectFLUOROPHORE-
dc.titleCoumarin-Derived Cu2+-Selective Fluorescence Sensor: Synthesis, Mechanisms, and Applications in Living Cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Jong Seung-
dc.identifier.doi10.1021/ja808611d-
dc.identifier.scopusid2-s2.0-67749114482-
dc.identifier.wosid000264792100069-
dc.identifier.bibliographicCitationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.131, no.5, pp.2008 - 2012-
dc.relation.isPartOfJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.titleJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.volume131-
dc.citation.number5-
dc.citation.startPage2008-
dc.citation.endPage2012-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusFLUORIDE-SELECTIVE FLUORESCENT-
dc.subject.keywordPlusHYDROGEN-PEROXIDE-
dc.subject.keywordPlusCU-II-
dc.subject.keywordPlusCOPPER-
dc.subject.keywordPlusION-
dc.subject.keywordPlusCHEMOSENSOR-
dc.subject.keywordPlusFLUOROIONOPHORE-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusZINC-
dc.subject.keywordPlusFLUOROPHORE-
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