Cation-Selective and Anion-Controlled Fluorogenic Behaviors of a Benzothiazole-Attached Macrocycle That Correlate with Structural Coordination Modes
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文摘
We report how the metal cation and its counteranions cooperate in the complexation-based macrocyclic chemosensor to monitor the target metal ion via the specific coordination modes. The benzothiazolyl group bearing NO<sub>2sub>S<sub>2sub>-macrocycle L was synthesized, and its mercury(II) selectivity (for perchlorate salt) as a dual-probe channel (UV–vis and fluorescence) chemosensor exhibiting the largest blue shift and the fluorescence turn-off was observed. In the mercury(II) sensing with different anions, except ClO<sub>4sub><sup>–sup> and NO<sub>3sub><sup>–sup>, no responses for mercury(II) were observed with other anions such as Cl<sup>–sup>, Br<sup>–sup>, I<sup>–sup>, SCN<sup>–sup>, OAc<sup>–sup>, and SO<sub>4sub><sup>2–sup>. A crystallographic approach for the mononuclear mercury(II) perchlorate complex [Hg(L)(ClO<sub>4sub>)<sub>2sub>]·0.67CH<sub>2sub>Cl<sub>2sub> (1) and polymeric mercury(II) iodide complex [Hg(L)I<sub>2sub>]<sub>nsub> (2) revealed that the observed anion-controlled mercury(II) sensing in the fluorescence mainly stems from the endo- and exocoordination modes, depending on the anion coordinating ability, which induces either the Hg–N<sub>tertsub> bond formation or not. The detailed complexation process with mercury(II) perchlorate associated with the cation sensing was also monitored with the titration methods by UV–vis, fluorescence spectroscopy, and cold-spray ionization mass spectrometry.

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