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Colorimetric detection of Cu(II): Cu(II)-induced deprotonation of NH responsible for color change

dc.citation.epage693en_US
dc.citation.issueen_US
dc.citation.spage688en_US
dc.citation.volume204en_US
dc.citation.woscount0
dc.contributor.authorKao, Shao-Lunen_US
dc.contributor.authorLin, Wan-Yingen_US
dc.contributor.authorVenkatesan, Parthibanen_US
dc.contributor.authorWu, Shu-Paoen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:36:55Z
dc.date.available2014-12-08T15:36:55Z
dc.date.issued2014-12-01en_US
dc.description.abstractChemosensor 1 detects only the presence of Cu2+ ions among other metal ions through a color change from pale yellow to green. 1 functions as a tridentate ligand that binds Cu2+ ions through three amine nitrogen functional groups. In the presence of Cu2+, 1 provided significant color change, while Ag+, Ca2+, Cd2+, Co2+, Fe2+, Fe3+, Hg2+, Mn2+, Ni2+, Pb2+, and Zn2+ metal ions produced only minor changes in UV-vis absorption. The association constant (Ka) for Cu2+ binding to 1 had a value of 1.307 x 10(3) M-1. The maximum absorption change induced by Cu2+ binding to the chemosensor was observed over the pH range 6.0-10.0. A new band observed at 600 nm indicated the formation of deprotonated 1-Cu2+ complexes. C) 2014 Elsevier B.V. All rights reserved.en_US
dc.identifier.doi10.1016/j.snb.2014.08.052en_US
dc.identifier.issn0925-4005en_US
dc.identifier.journalSENSORS AND ACTUATORS B-CHEMICALen_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.snb.2014.08.052en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/25308
dc.identifier.wosnumberWOS:000343116400087
dc.language.isoen_USen_US
dc.titleColorimetric detection of Cu(II): Cu(II)-induced deprotonation of NH responsible for color changeen_US
dc.typeArticleen_US

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