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作 者:Zhao,Bangtun Liu,Lianwei Li,Xiaochuan Qu,Guirong
机构地区:[1]Department of Chemistry,Luoyang Normal University,Luoyang,Henan 471022,China [2]College of Chemistry and Environmental Science,Henan Normal University,Xinxiang,Henan 453007,China
出 处:《Chinese Journal of Chemistry》2012年第2期254-258,共5页中国化学(英文版)
基 金:This work was supported by the National Natural Science Foundation of China (Grant Nos. 20872058, 21172105).
摘 要:A novel clicked tetrathiafulvalene derivative 3 bearing two 8-oxyquinoline groups was synthesized for the selective detection of Zn2+ through optical and electrochemical changes. The addition of Zn2+ and Cd2+ induced a significant change in fluorescence intensity, which was attributable to the chelation-enhanced fluorescence effect from the oxyquinoline and 1,2,3-triazole rings. The electrochemical potentials of 3 in the presence of the Zn2+ were shifted toward more positive values relative to those of the other metal cations tested.A novel clicked tetrathiafulvalene derivative 3 bearing two 8-oxyquinoline groups was synthesized for the selective detection of Zn2+ through optical and electrochemical changes. The addition of Zn2+ and Cd2+ induced a significant change in fluorescence intensity, which was attributable to the chelation-enhanced fluorescence effect from the oxyquinoline and 1,2,3-triazole rings. The electrochemical potentials of 3 in the presence of the Zn2+ were shifted toward more positive values relative to those of the other metal cations tested.
关 键 词:TETRATHIAFULVALENE 8-HYDROXYQUINOLINE click chemistry zinc ion
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