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Turn-on fluorescent capsule for selective fluoride detection and water purification

It has been a long-standing challenge to develop organic molecular capsules for selective anion binding in water. Here, selective recognition of aqueous fluoride was achieved through triple protonation of a hemicryptophane (L), which is composed of a fluorescent cyclotriveratrylene (CTV) cap and tri...

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Detalles Bibliográficos
Autores principales: Lin, Yannan, Du, Kang, Gau, Michael R., Dmochowski, Ivan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811533/
https://www.ncbi.nlm.nih.gov/pubmed/36687344
http://dx.doi.org/10.1039/d2sc05352g
Descripción
Sumario:It has been a long-standing challenge to develop organic molecular capsules for selective anion binding in water. Here, selective recognition of aqueous fluoride was achieved through triple protonation of a hemicryptophane (L), which is composed of a fluorescent cyclotriveratrylene (CTV) cap and tris(2-aminoethyl)amine (tren) as the anion binding site. Fluoride encapsulation by [3H-L](3+) was evidenced by (1)H NMR, (19)F NMR, LC-MS, and X-ray crystallography. In addition, [3H-L](3+) exhibited a ‘turn-on’ fluorescence signal (λ(em) = 324 nm) upon fluoride addition. An apparent association constant K(A) = (7.5 ± 0.4) × 10(4) M(−1) and a detection limit of 570 nM fluoride were extracted from the fluorescence titration experiments in citrate buffer at pH 4.1. To the best of our knowledge, [3H-L](3+) is the first example of a metal-free molecular capsule that reports on fluoride binding in purely aqueous solutions with a fluorescence response. Finally, the protonated capsule was supported on silica gel, which enabled adsorptive removal of stoichiometric fluoride from water and highlights real-world applications of this organic host–guest chemistry.