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dc.contributor.authorWu, Shu-Paoen_US
dc.contributor.authorDu, Kun-Juen_US
dc.contributor.authorSung, Yi-Mingen_US
dc.date.accessioned2014-12-08T15:07:45Z-
dc.date.available2014-12-08T15:07:45Z-
dc.date.issued2010en_US
dc.identifier.issn1477-9226en_US
dc.identifier.urihttp://hdl.handle.net/11536/6096-
dc.identifier.urihttp://dx.doi.org/10.1039/b925898aen_US
dc.description.abstract9,10-Anthraquinone-based chemosensor 1 indicates the presence of Cu(II) ions among other transition metal ions with high selectivity by a color change from yellow to dark red. Chemosensor 2 shows binding toward Cu(II), Ni(II) and Co(II) with color changes from yellow to dark red, red and pale green, respectively. Especially, Co(II) binding with chemosensor 2 causes significantly green fluorescence. On addition of Cu(II), 1 and 2 exhibit 76 and 80 nm red shifts in absorption wavelength (pH 7.0). The effect on pH by the formation of these 1-Cu(II) and 2-Cu(II) complexes was determined by UV-vis spectroscopic pH titration. In the pH range of 6-7.5, a maximum absorption was observed at 473 nm and exhibited the formation of deprotonated 1-Cu(II) and 2-Cu(II) complexes.en_US
dc.language.isoen_USen_US
dc.titleColorimetric sensing of Cu(II): Cu(II) induced deprotonation of an amide responsible for color changesen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/b925898aen_US
dc.identifier.journalDALTON TRANSACTIONSen_US
dc.citation.volume39en_US
dc.citation.issue18en_US
dc.citation.spage4363en_US
dc.citation.epage4368en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000277031800015-
dc.citation.woscount28-
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