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.
基金
This work was supported by the National Natural Science Foundation of China （Grant Nos. 20872058, 21172105）.
