Hydrogen bonding elements, π - hole functional moieties and C3v tripodal scaffold controlled turn-on cyanide and turn-off azide selective receptors.
Abstract
Here in, we are reporting electron deficient amide and sulfonamide based tripodal receptors L, L1, L2 and L3. Systematic studies show a strong selectivity towards cyanide and azide anions. Detailed UV–Visible and fluorescent spectrometric investigation shows the amide based tripodal receptors L and L3 acts as a colorimetric and turn-on fluorescent chemo-sensor for cyanide, and the sulfonamide based tripodal receptors L1 and L2 acts as a colorimetric and turn-off fluorescent chemo-sensor for azide. At the end we have successfully prepared tripodal receptors for a particular anion with judicious choice of recognition elements such as hydrogen bonding amide/sulfonamide moiety, electron deficient pentafluorophenyl functionality for anion-π interaction and the well defined C3v symmetric tripodal backbone for perfect recognition.
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| Fecha de publicación: | 2019 |
| URL: | https://link.springer.com/article/10.1007/s10895-020-02490-6 |