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Ratiometric determination of Hg2+ ions based on simple molecular motifs of pyrene and dioxaoctanediamide

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dc.contributor.authorKim, Jun Soo-
dc.contributor.authorChoi, Myung Gil-
dc.contributor.authorSong, Ki Cheol-
dc.contributor.authorNo, Kyoung Tai-
dc.contributor.authorAhn, Sangdoo-
dc.contributor.authorChang, Suk-Kyu-
dc.date.available2019-05-30T06:34:44Z-
dc.date.issued2007-03-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24124-
dc.description.abstractA new podand-type dioxaoctanediamide-based chemosensor having two pyrene moieties was prepared, and its fluoroionophoric behaviors toward transition-metal ions were investigated. Pyrene-appended dioxaoctanediamide 1 showed a selective fluorescence quenching toward Hg2+ ions over other transition-metal ions in an aqueous methanol solution. Unique responses in pyrene monomer and excimer emissions allowed selective ratiometric determination of Hg2+ ions in aqueous environments, and the detection limit was found to be 1.6 x 10(-6) M.-
dc.format.extent4-
dc.language영어-
dc.language.isoENG-
dc.publisherAMER CHEMICAL SOC-
dc.titleRatiometric determination of Hg2+ ions based on simple molecular motifs of pyrene and dioxaoctanediamide-
dc.typeArticle-
dc.identifier.doi10.1021/ol070143r-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.9, no.6, pp 1129 - 1132-
dc.description.isOpenAccessN-
dc.identifier.wosid000244735900046-
dc.identifier.scopusid2-s2.0-33947602175-
dc.citation.endPage1132-
dc.citation.number6-
dc.citation.startPage1129-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume9-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordPlusSELECTIVE FLUORESCENT SENSOR-
dc.subject.keywordPlusTRANSITION-METAL IONS-
dc.subject.keywordPlusAQUEOUS-SOLUTION-
dc.subject.keywordPlusEXCIMER FLUORESCENCE-
dc.subject.keywordPlusENERGY-TRANSFER-
dc.subject.keywordPlusHG(II) SENSOR-
dc.subject.keywordPlusMERCURIC ION-
dc.subject.keywordPlusCHEMOSENSOR-
dc.subject.keywordPlusMEDIA-
dc.subject.keywordPlusLEAD-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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