<i>Cinchona</i> alkaloid copolymers as fluorimetric INHIBIT and colorimetric AND logic gates for detection of iodide

Four <i>cinchona</i> alkaloid-acrylamide water soluble copolymers with a mean hydrodynamic diameter of 3 nm were synthesised by free radical polymerization. The copolymers were characterised by <sup>1</sup>H NMR, FTIR, GPC, DLS, UV-vis and fluorescence spectroscopy. A blue emission is observed with H<sup>+</sup> 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<sup>-</sup>, Br<sup>-</sup> or I<sup>-</sup> causes fluorescence quenching. In emission mode, the copolymers function as fluorescent H<sup>+</sup>, X<sup>-</sup>-driven INHIBIT logic gates (where X = Cl<sup>-</sup>, Br<sup>-</sup> or I<sup>-</sup>). In absorbance mode, the copolymers function as colorimetric H<sup>+</sup>, I<sup>-</sup>-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.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra01281c
Citations
2
Primary Topic
Molecular Sensors and Ion Detection
Type
article
Field-Weighted Citation Impact
1.51

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article

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

David C. Magri, Nicola’ Agius, Helen Willcock, Catherine J. Ashton
2 citations
RSC Advances
Molecular Sensors and Ion Detection
1.51
article

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

David C. Magri, Nicola’ Agius, Helen Willcock, Catherine J. Ashton
article en
2 citations

Abstract

Four <i>cinchona</i> alkaloid-acrylamide water soluble copolymers with a mean hydrodynamic diameter of 3 nm were synthesised by free radical polymerization. The copolymers were characterised by <sup>1</sup>H NMR, FTIR, GPC, DLS, UV-vis and fluorescence spectroscopy. A blue emission is observed with H<sup>+</sup> 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<sup>-</sup>, Br<sup>-</sup> or I<sup>-</sup> causes fluorescence quenching. In emission mode, the copolymers function as fluorescent H<sup>+</sup>, X<sup>-</sup>-driven INHIBIT logic gates (where X = Cl<sup>-</sup>, Br<sup>-</sup> or I<sup>-</sup>). In absorbance mode, the copolymers function as colorimetric H<sup>+</sup>, I<sup>-</sup>-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.

RSC AdvancesVol. 15(14)
Loughborough University (GB), University of Malta (MT)
Engineering and Physical Sciences Research Council
Clean water and sanitation
Openalex Percentile: Top 20%
Molecular Sensors and Ion Detection
1.51
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<i>Cinchona</i> alkaloid copolymers as fluorimetric INHIBIT and colorimetric AND logic gates for detection of iodide — David C. Magri, Nicola’ Agius, et al. · RSC Advances (2025) | TGRS Research Map | TGRS