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A benzothiazole-based new fluorogenic chemosensor for the detection of CN(−) and its real-time application in environmental water samples and living cells
Since the cyanide ion is used in a wide range of industries and is harmful to both human health and the environment, a number of research efforts are dedicated to creating fluorescence sensors for the detection of cyanide (CN(−)). Herein, for the fluorescence detection of CN(−), a new highly selecti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984840/ https://www.ncbi.nlm.nih.gov/pubmed/35424806 http://dx.doi.org/10.1039/d1ra08846g |
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author | Jothi, Dhanapal Munusamy, Sathishkumar Manoj kumar, Selin Enbanathan, Saravanan Kulathu Iyer, Sathiyanarayanan |
author_facet | Jothi, Dhanapal Munusamy, Sathishkumar Manoj kumar, Selin Enbanathan, Saravanan Kulathu Iyer, Sathiyanarayanan |
author_sort | Jothi, Dhanapal |
collection | PubMed |
description | Since the cyanide ion is used in a wide range of industries and is harmful to both human health and the environment, a number of research efforts are dedicated to creating fluorescence sensors for the detection of cyanide (CN(−)). Herein, for the fluorescence detection of CN(−), a new highly selective and sensitive sensor 2-(3-(benzo[d]thiazol-2-yl)-4-hydroxybenzylidene)-1H-indene-1,3(2H)-dione (BID) was created by conjugating a benzothiazole moiety with 1H-indene-1,3(2H)-dione. The donor and acceptor components of this hybrid receptor were covalently connected through a double bond. The nucleophilic addition of a cyanide anion to the BID inhibits the intramolecular charge transfer (ICT) transition, resulting in spectral and colour alterations in the receptor. When the solvent polarity was increased from n-hexane to methanol, this molecule exhibited a bathochromic shift in the emission wavelength (610 to 632 nm), suggesting the presence of a solvatochromic action. The sensor BID has shown strong specificity towards CN(−) by interrupting its internal charge transfer (ICT), resulting in a significant change in the UV-vis spectrum and a notable blue shift in the fluorescence emission spectrum. The cyanide anion (CN(−)) is responsible for the optical alterations observed by BID, as opposed to the other anions examined. The detection limit was 5.97 nM, significantly less than the WHO's permitted amount of CN(−) in drinking water. The experimental findings indicate that BID's fluorescence response to CN(−) is pH insensitive throughout a wide pH range of 6.0 to 12.0. The interaction mechanism between the BID and CN(−) ions has been studied by HRMS, (1)H-NMR titration experiments, FT-IR, and DFT, which confirmed the nucleophilic addition of CN(−) on vinylidene and subsequent disturbance of ICT. Additionally, we demonstrated the real-time detection application of CN(−) in environmental water samples and live-cell imaging. |
format | Online Article Text |
id | pubmed-8984840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-89848402022-04-13 A benzothiazole-based new fluorogenic chemosensor for the detection of CN(−) and its real-time application in environmental water samples and living cells Jothi, Dhanapal Munusamy, Sathishkumar Manoj kumar, Selin Enbanathan, Saravanan Kulathu Iyer, Sathiyanarayanan RSC Adv Chemistry Since the cyanide ion is used in a wide range of industries and is harmful to both human health and the environment, a number of research efforts are dedicated to creating fluorescence sensors for the detection of cyanide (CN(−)). Herein, for the fluorescence detection of CN(−), a new highly selective and sensitive sensor 2-(3-(benzo[d]thiazol-2-yl)-4-hydroxybenzylidene)-1H-indene-1,3(2H)-dione (BID) was created by conjugating a benzothiazole moiety with 1H-indene-1,3(2H)-dione. The donor and acceptor components of this hybrid receptor were covalently connected through a double bond. The nucleophilic addition of a cyanide anion to the BID inhibits the intramolecular charge transfer (ICT) transition, resulting in spectral and colour alterations in the receptor. When the solvent polarity was increased from n-hexane to methanol, this molecule exhibited a bathochromic shift in the emission wavelength (610 to 632 nm), suggesting the presence of a solvatochromic action. The sensor BID has shown strong specificity towards CN(−) by interrupting its internal charge transfer (ICT), resulting in a significant change in the UV-vis spectrum and a notable blue shift in the fluorescence emission spectrum. The cyanide anion (CN(−)) is responsible for the optical alterations observed by BID, as opposed to the other anions examined. The detection limit was 5.97 nM, significantly less than the WHO's permitted amount of CN(−) in drinking water. The experimental findings indicate that BID's fluorescence response to CN(−) is pH insensitive throughout a wide pH range of 6.0 to 12.0. The interaction mechanism between the BID and CN(−) ions has been studied by HRMS, (1)H-NMR titration experiments, FT-IR, and DFT, which confirmed the nucleophilic addition of CN(−) on vinylidene and subsequent disturbance of ICT. Additionally, we demonstrated the real-time detection application of CN(−) in environmental water samples and live-cell imaging. The Royal Society of Chemistry 2022-03-18 /pmc/articles/PMC8984840/ /pubmed/35424806 http://dx.doi.org/10.1039/d1ra08846g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Jothi, Dhanapal Munusamy, Sathishkumar Manoj kumar, Selin Enbanathan, Saravanan Kulathu Iyer, Sathiyanarayanan A benzothiazole-based new fluorogenic chemosensor for the detection of CN(−) and its real-time application in environmental water samples and living cells |
title | A benzothiazole-based new fluorogenic chemosensor for the detection of CN(−) and its real-time application in environmental water samples and living cells |
title_full | A benzothiazole-based new fluorogenic chemosensor for the detection of CN(−) and its real-time application in environmental water samples and living cells |
title_fullStr | A benzothiazole-based new fluorogenic chemosensor for the detection of CN(−) and its real-time application in environmental water samples and living cells |
title_full_unstemmed | A benzothiazole-based new fluorogenic chemosensor for the detection of CN(−) and its real-time application in environmental water samples and living cells |
title_short | A benzothiazole-based new fluorogenic chemosensor for the detection of CN(−) and its real-time application in environmental water samples and living cells |
title_sort | benzothiazole-based new fluorogenic chemosensor for the detection of cn(−) and its real-time application in environmental water samples and living cells |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984840/ https://www.ncbi.nlm.nih.gov/pubmed/35424806 http://dx.doi.org/10.1039/d1ra08846g |
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