Home > Research > Publications & Outputs > Cinchona alkaloid copolymers as fluorimetric IN...

Links

Text available via DOI:

View graph of relations

Cinchona alkaloid copolymers as fluorimetric INHIBIT and colorimetric AND logic gates for detection of iodide

Research output: Contribution to Journal/MagazineJournal articlepeer-review

E-pub ahead of print
Close
<mark>Journal publication date</mark>8/04/2025
<mark>Journal</mark>RSC Advances
Issue number14
Volume15
Number of pages7
Pages (from-to)11121-11127
Publication StatusE-pub ahead of print
Early online date8/04/25
<mark>Original language</mark>English

Abstract

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.