Abstract

A novel dual emissive fluorescent probe SFQ was designed and synthesized by linking dicyanisophorone and thiophene aldehyde units to carbazole groups. The probe SFQ has high selectivity and sensitivity toward ClO−. Upon addition of ClO− to the solution of probe SFQ resulted in a noticeable color changed from orange to pink under natural light. Meanwhile, SFQ could make a ratiometric fluorescence response to ClO− at two different excitation wavelengths, with the change of color from orange-red fluorescence to cyan fluorescence under the 365 nm UV lamp. The detection limit was 1.4 × 10−7 mol/L under ratiometric conditions. The study on the reaction mechanism showed that when SFQ reacted with ClO−, the cyano group disappeared and the cyclic ketone SFQ-O came into being. Furthermore, probe SFQ was successfully used to monitor ClO− in HepG2 cells and detect ClO− in actual environmental water samples.

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