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A novel intramolecular charge transfer fluorescent
chemosensor highly selective for Cu 2+ in
neutral aqueous solutions |
Qingxian LIAO1,Aifang LI2,Zhao LI2,Yibin RUAN2,Yunbao JIANG2, |
1.Department of Chemistry,
College of Chemistry and Chemical Engineering, and Key Laboratory
of Analytical Sciences, Xiamen University, Xiamen 361005, China;Xiamen Water Group Co.
Ltd., Xiamen 361008, China; 2.Department of Chemistry,
College of Chemistry and Chemical Engineering, and Key Laboratory
of Analytical Sciences, Xiamen University, Xiamen 361005, China; |
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Abstract A selective and sensitive intramolecular charge transfer (ICT) fluorescent chemosensor was designed for Cu2+ in neutral aqueous solutions of pH 7.0. The design of this totally water-soluble fluorescent chemosensor was based on the binding motif of Cu2+ to aminoacid, which is coupled to an ICT fluorophore bearing a 1,3,4-thiodiazole moiety in the electron acceptor. The formation of a 1:1 complex of Cu2+ to 2 was suggested to lead to fluorescence quenching. The quenching obeyed Stern-Volmer theory in neutral aqueous solution of pH 7.0 for Cu2+ over 5.0 × 10−7 to 3.0 × 10−5 mol·L−1, with a quenching constant of 1.8 × 105 L·mol−1 and a detection limit of 2.0 × 10−7 mol·L−1. The binding of Cu2+ to 2 can be fully reversed by addition of chelator EDTA, affording a reversible sensing performance.
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Keywords
fluorescent chemosensor
Cu2+
fluorescence quenching
intramolecular charge transfer
4-thiodiazole
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Issue Date: 05 June 2010
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