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Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies
High toxicity and extensive accessibility of fluoride and cyanide ions in diverse environmental media encouraged attention for scheming well-organized probes for their detection. Keeping in mind we have designed and synthesized thiosemicarbazone-based chemosensors RB-1, RB-2 and RB-3 for the detecti...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943172/ https://www.ncbi.nlm.nih.gov/pubmed/35322108 http://dx.doi.org/10.1038/s41598-022-08860-3 |
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author | Basri, Rabia Ahmed, Nadeem Khalid, Muhammad Khan, Muhammad Usman Abdullah, Muhammad Syed, Asad Elgorban, Abdallah M. Al-Rejaie, Salim S. Braga, Ataualpa Albert Carmo Shafiq, Zahid |
author_facet | Basri, Rabia Ahmed, Nadeem Khalid, Muhammad Khan, Muhammad Usman Abdullah, Muhammad Syed, Asad Elgorban, Abdallah M. Al-Rejaie, Salim S. Braga, Ataualpa Albert Carmo Shafiq, Zahid |
author_sort | Basri, Rabia |
collection | PubMed |
description | High toxicity and extensive accessibility of fluoride and cyanide ions in diverse environmental media encouraged attention for scheming well-organized probes for their detection. Keeping in mind we have designed and synthesized thiosemicarbazone-based chemosensors RB-1, RB-2 and RB-3 for the detection of fluoride and cyanide ions. The structural elucidation of the synthesized chemosensors is done by employing different analytical techniques including nuclear magnetic resonance and electronic absorption specrtoscopies. Admirable detection limit, binding constant and fast response time (2 s) to F(−) and CN(−) ions enlarged the applications of these chemosensors. Additional confirmation of the sensing ability of these chemosensors is derived from DFT and TDDFT calculations with M06/6-311G(d,p) method by performing FMO, UV–Vis, QTAIM and global reactivity parameters elucidation. Overall results point out that investigated chemosensors are suitable candidates for sensing the F(−) ions. These chemosensors were successfully applied to detect F(−) ions in a commercial toothpaste sample. |
format | Online Article Text |
id | pubmed-8943172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89431722022-03-28 Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies Basri, Rabia Ahmed, Nadeem Khalid, Muhammad Khan, Muhammad Usman Abdullah, Muhammad Syed, Asad Elgorban, Abdallah M. Al-Rejaie, Salim S. Braga, Ataualpa Albert Carmo Shafiq, Zahid Sci Rep Article High toxicity and extensive accessibility of fluoride and cyanide ions in diverse environmental media encouraged attention for scheming well-organized probes for their detection. Keeping in mind we have designed and synthesized thiosemicarbazone-based chemosensors RB-1, RB-2 and RB-3 for the detection of fluoride and cyanide ions. The structural elucidation of the synthesized chemosensors is done by employing different analytical techniques including nuclear magnetic resonance and electronic absorption specrtoscopies. Admirable detection limit, binding constant and fast response time (2 s) to F(−) and CN(−) ions enlarged the applications of these chemosensors. Additional confirmation of the sensing ability of these chemosensors is derived from DFT and TDDFT calculations with M06/6-311G(d,p) method by performing FMO, UV–Vis, QTAIM and global reactivity parameters elucidation. Overall results point out that investigated chemosensors are suitable candidates for sensing the F(−) ions. These chemosensors were successfully applied to detect F(−) ions in a commercial toothpaste sample. Nature Publishing Group UK 2022-03-23 /pmc/articles/PMC8943172/ /pubmed/35322108 http://dx.doi.org/10.1038/s41598-022-08860-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Basri, Rabia Ahmed, Nadeem Khalid, Muhammad Khan, Muhammad Usman Abdullah, Muhammad Syed, Asad Elgorban, Abdallah M. Al-Rejaie, Salim S. Braga, Ataualpa Albert Carmo Shafiq, Zahid Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies |
title | Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies |
title_full | Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies |
title_fullStr | Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies |
title_full_unstemmed | Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies |
title_short | Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies |
title_sort | quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and dft studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943172/ https://www.ncbi.nlm.nih.gov/pubmed/35322108 http://dx.doi.org/10.1038/s41598-022-08860-3 |
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