Abstract
Conjugated 5,5′-Bicalixarene scaffolds having fluorophores at the chain termini have been prepared and tested in the supramolecular detection of nitric oxide. Scaffolds bearing electron-rich fluorophores demonstrated a stronger turn-off response to the presence of NO than the fluorophore-free analogue in both organic and aqueous media, while no fluorescence quenching happened when the electron-deficient fluorophores were employed. Unprecedented ratiometric supramolecular sensing was observed when fluorophores of the opposite electronic demands were placed at the scaffold's termini.
| Original language | English |
|---|---|
| Pages (from-to) | 9706-9711 |
| Number of pages | 6 |
| Journal | Organic Letters |
| Volume | 22 |
| Issue number | 24 |
| DOIs | |
| State | Published - 18 Dec 2020 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
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