Final published version
Licence: CC BY
Research output: Contribution to Journal/Magazine › Journal article › peer-review
<mark>Journal publication date</mark> | 8/04/2025 |
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<mark>Journal</mark> | RSC Advances |
Issue number | 14 |
Volume | 15 |
Number of pages | 7 |
Pages (from-to) | 11121-11127 |
Publication Status | E-pub ahead of print |
Early online date | 8/04/25 |
<mark>Original language</mark> | English |
Four cinchona alkaloid-acrylamide water soluble copolymers with a mean hydrodynamic diameter of 3 nm were synthesised by free radical polymerization. The copolymers were characterised by 1H NMR, FTIR, GPC, DLS, UV-vis and fluorescence spectroscopy. A blue emission is observed with H + switching of 185 and 175-fold for the quinidine and quinine copolymers, and 21 and 11-fold for the cinchonine and cinchonidine copolymers, while the presence of Cl -, Br - or I - causes fluorescence quenching. In emission mode, the copolymers function as fluorescent H +, X --driven INHIBIT logic gates (where X = Cl -, Br - or I -). In absorbance mode, the copolymers function as colorimetric H +, I --driven AND logic gates in 1 : 1 (v/v) THF/water with a 76-fold enhancement. The solution colour changes from colourless to yellow with formation of new absorbance bands at 288 nm and 353 nm due to a π-anion non-covalent charge transfer interaction. The copolymers may be useful as selective iodide sensors for medical and analytical diagnostics.