Anion Association and Macrocycle Encapsulation Tune the Fluorescence of N-Alkylpyridinium-Conjugated Push-Pull Thiazolothiazole Derivatives

阴离子缔合和大环包封调节N-烷基吡啶鎓共轭推拉噻唑并噻唑衍生物的荧光

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Abstract

The fluorescence properties of N-alkylpyridinium-conjugated thiazolothiazole (TTZ) fluorophores can be effectively modulated through counterion pairing and macrocyclic encapsulation. A distinct blue emission response to the iodide counterion offers potential applications in anion sensing. Host-guest complexation at the pyridinium site with macrocyclic receptors significantly perturbs the electronic environment of the TTZ core, enabling reversible dual-color emission.

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