摘要
The sensitive detection and quantification of heavy and transition metal ions are particularly important. Among them, mercury(II) (Hg 2+ ) and silver(I) (Ag + ) ions, as the most ubiquitous heavy metal ion pollutants, are difficult to discriminate in the same system because of their similar reactions and coordination abilities. Herein, we designed and synthesized a “turn-on” chemosensor, RBTP , which is an intergrant of rhodol and 2-hydroxy benzothiazole by introducing a benzothiazole unit to the ortho -position of the phenolic hydroxy of rhodol. RBTP showed a sensitive dual-channel fluorescence-enhanced response to Hg 2+ and Ag + at 595 and 520 nm with low detection limits of 0.27 and 0.45 μM, respectively. Studies of their sensing mechanism indicated that the Hg 2+ -induced orange fluorescence at 595 nm originates from an irreversible Hg 2+ -promoted oxadiazole forming reaction and the Ag + -induced green fluorescence at 520 nm originates from special molecular packing of the RBTP -Ag + complex. Furthermore, the potential of probe RBTP as practical biological imaging agents was further confirmed in HepG2 cells. Simultaneously, RBTP exhibited remarkable solid-state luminescence with an aggregation-induced emission (AIE) feature. The AIE mechanism was thoroughly explored using X-ray single-crystal structures and photophysical determinations.
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