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dc.contributor.authorChang, Kai-Chien_US
dc.contributor.authorLuo, Li-Yangen_US
dc.contributor.authorDiau, Eric Wei-Guangen_US
dc.contributor.authorChung, Wen-Shengen_US
dc.date.accessioned2014-12-08T15:11:02Z-
dc.date.available2014-12-08T15:11:02Z-
dc.date.issued2008-08-18en_US
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.tetlet.2008.06.060en_US
dc.identifier.urihttp://hdl.handle.net/11536/8455-
dc.description.abstractA novel fluorescent chemosensor 1 with two anthraceneisoxazolymethyl groups at the lower rim of calix[4]arene has been synthesized, which revealed a dual emission (monomer and excimer) when excited at 375 nm. This chemosensor displayed a selective fluorescence quenching only with Cu(2+) ion over all other metal ions examined. When Cu(2+) ion was bound to 1, the fluorescence intensities of both monomer and excimer were quenched. Furthermore, the association constant for the 1:1 complex of 1.Cu(2+) was determined to be (1.58 +/- 0.03) x 10(4) M(-1). (c) 2008 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleHighly selective fluorescent sensing of Cu(2+) ion by an arylisoxazole modified calix[4]areneen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tetlet.2008.06.060en_US
dc.identifier.journalTETRAHEDRON LETTERSen_US
dc.citation.volume49en_US
dc.citation.issue34en_US
dc.citation.spage5013en_US
dc.citation.epage5016en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000258271400007-
dc.citation.woscount35-
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