A Novel Colorimetric and Fluorometric Dual‐Channel Chemosensor based on A Conjugated Perylene‐Benzothiazole System for Highly Selective Detection of Cyanide in Aqueous Media

A novel cyanine compound based on the conjugated perylene‐benzothiazole system (PBI) as a colorimetric and fluorometric dual‐channel sensor for cyanide (CN−) detection was synthesized and characterized via UV‐vis and fluorescence spectroscopy. PBI exhibited a high sensitivity and rapid optical respo...

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Published inChemPlusChem (Weinheim, Germany) Vol. 88; no. 8; pp. e202300264 - n/a
Main Authors Nguyen, Thao Phuong Le, Nguyen, Cam Hong Thi, Nguyen, Thiet‐Quoc, Tran, Chau Duc, Nguyen, Tam Huu, Nguyen, Le‐Thu T., Nguyen, Ha Tran
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 01.08.2023
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Summary:A novel cyanine compound based on the conjugated perylene‐benzothiazole system (PBI) as a colorimetric and fluorometric dual‐channel sensor for cyanide (CN−) detection was synthesized and characterized via UV‐vis and fluorescence spectroscopy. PBI exhibited a high sensitivity and rapid optical response for CN− due to the intramolecular charge transfer (ICT) mechanism. The detection limit of PBI for CN− was 1.15×10−7 M in the mixture of DMSO/H2O (1 : 1, v/v). Moreover, probe PBI demonstrated high selectivity and sensitivity for CN− over other common anions, including Cl−, Br−, F−, I−, AcO−, ClO4−, HSO4−, SO42−, NO2−, NO3− and SCN−. This work provided a simple and effective approach to trace the toxic CN− ion with rapid response, high selectivity, and sensitivity that is possibly applied in environmental control and agricultural management. A novel cyanide chemosensor (PBI) was synthesized from perylene and 3‐ethyl‐2‐methylbenzothiazolium iodide via Knoevenagel condensation reaction. The conjugated molecule is a naked‐eye detection with highly sensitive and selectivity for cyanide due to the intramolecular charge transfer (ICT) mechanism. The detection limit of PBI to cyanide anion is 1.15×10−7 M with the color change from red‐violet to yellow.
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ISSN:2192-6506
2192-6506
DOI:10.1002/cplu.202300264