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Thiophene-Appended Benzothiazole Compounds for Ratiometric Detection of Copper and Cadmium Ions with Comparative Density Functional Theory Studies and Their Application in Real-Time Samples
[Image: see text] A thirst for the development of a simple fluorescence probe for enhanced sensing application has been achieved by synthesizing a stupendous thiophene-appended benzothiazole-conjugated compound L2. The synthesized compound L2 was characterized using nuclear magnetic resonance and ma...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9670728/ https://www.ncbi.nlm.nih.gov/pubmed/36406525 http://dx.doi.org/10.1021/acsomega.2c05157 |
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author | Purushothaman, Palani Karpagam, Subramanian |
author_facet | Purushothaman, Palani Karpagam, Subramanian |
author_sort | Purushothaman, Palani |
collection | PubMed |
description | [Image: see text] A thirst for the development of a simple fluorescence probe for enhanced sensing application has been achieved by synthesizing a stupendous thiophene-appended benzothiazole-conjugated compound L2. The synthesized compound L2 was characterized using nuclear magnetic resonance and mass spectrometry techniques. Furthermore, a photophysical property of L1 and L2 reveals the enhanced emission spectrum of L2 because of a restricted spin–orbital coupling as a result of increased conjugation compared to the ligand L1. Therefore, comparative studies were undertaken for L1 and L2. Henceforth, L2 was deployed for the ratiometric detection of Cd(2+) ions in THF:water and L1 for the detection of Cu(2+) ions in THF medium. The chemosensor L2 shows an outstanding water tolerance up to 60% and is stable between pH 2 and 7. This level of water tolerance and stability make L2 a suitable probe for analyzing real-time and biological samples. While the cadmium ion was added to L2, there was a significant red shift in emission from 496 to 549 nm, which indicates the controlled ICT due to complex formation. The metal–ligand complexation was also confirmed by noticing a decreased band gap of metal complex compared to the ligand as calculated using Tauc’s plot with solid-phase UV data. The stoichiometric ratio was obtained by Job’s plot that exhibited a 1:1 ratio of L2 and Cd(2+) ions, and the limit of detection (LOD) was found to be 2.25 nM by the photoluminescence spectroscopic technique. The fluorescence lifetime of both L2 and L2-Cd(2+) was found to be 58.3 ps and 0.147 ns, respectively. Alongside, the colorimetric-assisted ratiometric detection of Cu(2+) by L1 with 1:2 stoichiometric ratio having an LOD of 1.06 × 10(–7) M was also performed. Furthermore, the practical applicability of the probe L2 in sensing cadmium was tested in sewage water and vegetable extract; the recovery was approximately 98 and 99%, respectively. The experimental data were supported by theoretical investigation of structures of L1, L2, L1-Cu(2+), and L2-Cd(2+), complex formation, charge transfer mechanism, and band gap measurements done by quantum chemical density functional theory calculations. |
format | Online Article Text |
id | pubmed-9670728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96707282022-11-18 Thiophene-Appended Benzothiazole Compounds for Ratiometric Detection of Copper and Cadmium Ions with Comparative Density Functional Theory Studies and Their Application in Real-Time Samples Purushothaman, Palani Karpagam, Subramanian ACS Omega [Image: see text] A thirst for the development of a simple fluorescence probe for enhanced sensing application has been achieved by synthesizing a stupendous thiophene-appended benzothiazole-conjugated compound L2. The synthesized compound L2 was characterized using nuclear magnetic resonance and mass spectrometry techniques. Furthermore, a photophysical property of L1 and L2 reveals the enhanced emission spectrum of L2 because of a restricted spin–orbital coupling as a result of increased conjugation compared to the ligand L1. Therefore, comparative studies were undertaken for L1 and L2. Henceforth, L2 was deployed for the ratiometric detection of Cd(2+) ions in THF:water and L1 for the detection of Cu(2+) ions in THF medium. The chemosensor L2 shows an outstanding water tolerance up to 60% and is stable between pH 2 and 7. This level of water tolerance and stability make L2 a suitable probe for analyzing real-time and biological samples. While the cadmium ion was added to L2, there was a significant red shift in emission from 496 to 549 nm, which indicates the controlled ICT due to complex formation. The metal–ligand complexation was also confirmed by noticing a decreased band gap of metal complex compared to the ligand as calculated using Tauc’s plot with solid-phase UV data. The stoichiometric ratio was obtained by Job’s plot that exhibited a 1:1 ratio of L2 and Cd(2+) ions, and the limit of detection (LOD) was found to be 2.25 nM by the photoluminescence spectroscopic technique. The fluorescence lifetime of both L2 and L2-Cd(2+) was found to be 58.3 ps and 0.147 ns, respectively. Alongside, the colorimetric-assisted ratiometric detection of Cu(2+) by L1 with 1:2 stoichiometric ratio having an LOD of 1.06 × 10(–7) M was also performed. Furthermore, the practical applicability of the probe L2 in sensing cadmium was tested in sewage water and vegetable extract; the recovery was approximately 98 and 99%, respectively. The experimental data were supported by theoretical investigation of structures of L1, L2, L1-Cu(2+), and L2-Cd(2+), complex formation, charge transfer mechanism, and band gap measurements done by quantum chemical density functional theory calculations. American Chemical Society 2022-11-02 /pmc/articles/PMC9670728/ /pubmed/36406525 http://dx.doi.org/10.1021/acsomega.2c05157 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Purushothaman, Palani Karpagam, Subramanian Thiophene-Appended Benzothiazole Compounds for Ratiometric Detection of Copper and Cadmium Ions with Comparative Density Functional Theory Studies and Their Application in Real-Time Samples |
title | Thiophene-Appended
Benzothiazole Compounds for Ratiometric
Detection of Copper and Cadmium Ions with Comparative Density Functional
Theory Studies and Their Application in Real-Time Samples |
title_full | Thiophene-Appended
Benzothiazole Compounds for Ratiometric
Detection of Copper and Cadmium Ions with Comparative Density Functional
Theory Studies and Their Application in Real-Time Samples |
title_fullStr | Thiophene-Appended
Benzothiazole Compounds for Ratiometric
Detection of Copper and Cadmium Ions with Comparative Density Functional
Theory Studies and Their Application in Real-Time Samples |
title_full_unstemmed | Thiophene-Appended
Benzothiazole Compounds for Ratiometric
Detection of Copper and Cadmium Ions with Comparative Density Functional
Theory Studies and Their Application in Real-Time Samples |
title_short | Thiophene-Appended
Benzothiazole Compounds for Ratiometric
Detection of Copper and Cadmium Ions with Comparative Density Functional
Theory Studies and Their Application in Real-Time Samples |
title_sort | thiophene-appended
benzothiazole compounds for ratiometric
detection of copper and cadmium ions with comparative density functional
theory studies and their application in real-time samples |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9670728/ https://www.ncbi.nlm.nih.gov/pubmed/36406525 http://dx.doi.org/10.1021/acsomega.2c05157 |
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