Colorimetric chemosensors for the selective detection of arsenite over arsenate anions in aqueous medium: Application in environmental water samples and DFT studies

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Date

2023

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Elsevier B.V.

Abstract

Novel organic receptors N3R1- N3R3 were developed for the selective colorimetric recognition of arsenite ions in the organo-aqueous media. In the 50% aq. acetonitrile media and 70% aq. DMSO media, receptors N3R2 and N3R3 showed specific sensitivity and selectivity towards arsenite anions over arsenate anions. Receptor N3R1 showed discriminating recognition of arsenite in the 40% aq. DMSO medium. All three receptors formed a 1:1 complex with arsenite and stable for a pH range of 6–12. The receptors N3R2 and N3R3 achieved a detection limit of 0.008 ppm (8 ppb) and 0.0246 ppm, respectively, for arsenite. Initial hydrogen bonding on binding with the arsenite followed by the deprotonation mechanism was well supported by the UV–Vis titration, 1H- NMR titration, electrochemical studies, and the DFT studies. Colorimetric test strips were fabricated using N3R1- N3R3 for the on-site detection of arsenite anion. The receptors are also employed for sensing arsenite ions in various environmental water samples with high accuracy. © 2023 Elsevier B.V.

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Keywords

Color, Colorimetry, Design for testability, Hydrogen bonds, Titration, Aqueous media, Arsenate anions, Arsenite, Colorimetric chemosensor, DFT study, Environmental water analysis, Environmental water samples, Media application, Selective detection, Test strips, Negative ions, acetonitrile, arsenic acid, arsenic trioxide, dimethyl sulfoxide, hydrogen, N3R1 receptor, N3R3 receptor, receptor, unclassified drug, accuracy, Article, association constant, chemical binding, colorimetry, density functional theory, deprotonation, electrochemistry, hydrogen bond, limit of detection, molecular recognition, molecular stability, pH measurement, proton nuclear magnetic resonance, sensitivity and specificity, ultraviolet spectroscopy, water sampling

Citation

Analytica Chimica Acta, 2023, 1265, , pp. -

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