Anion Association and Macrocycle Encapsulation Tune the Fluorescence of <i>N</i>-Alkylpyridinium-Conjugated Push–Pull Thiazolothiazole Derivatives
The fluorescence properties of <i>N</i>-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.
Authors
- Kanhu Charan Behera (ORCID: https://orcid.org/0000-0002-4016-9033)
- Sheng‐Hsien Chiu (ORCID: https://orcid.org/0000-0002-0040-1555)
- Chih‐Yu Kuo (ORCID: https://orcid.org/0000-0002-1211-6700)
- Chia-Chun Liu (ORCID: https://orcid.org/0000-0002-9823-255X)
Institutions
- National Taiwan University (TW)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-09-26
- DOI
- https://doi.org/10.1021/acs.orglett.5c03338
- Primary Topic
- Luminescence and Fluorescent Materials
- Type
- article
- Field-Weighted Citation Impact
- 0.00