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Thiazole-Formulated Azomethine Compound for Three-Way Detection of Mercury Ions in Aqueous Media and Application in Living Cells
[Image: see text] Heavy metal ions are extremely poisonous and cause long-term harm to living organisms. Among these ions, mercury is the most toxic metal and has no notorious purpose in the human body. In this regard, an elegant azomethine thiazole compound AM1 was synthesized, and it was found to...
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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/PMC9301703/ https://www.ncbi.nlm.nih.gov/pubmed/35874226 http://dx.doi.org/10.1021/acsomega.2c02473 |
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author | Umabharathi, Pushparani Selvakumar Karpagam, Subramanian |
author_facet | Umabharathi, Pushparani Selvakumar Karpagam, Subramanian |
author_sort | Umabharathi, Pushparani Selvakumar |
collection | PubMed |
description | [Image: see text] Heavy metal ions are extremely poisonous and cause long-term harm to living organisms. Among these ions, mercury is the most toxic metal and has no notorious purpose in the human body. In this regard, an elegant azomethine thiazole compound AM1 was synthesized, and it was found to be highly sensitive to three-way detection of mercury ions with detection limits of 0.1126 × 10(–9) M (FL) and 0.64 × 10(–6) M (UV–vis). AM1 highlighted the capability to detect mercury ions through the colorimetric method, the fluorometric method, and via the naked eye in three-way detection. In addition, the structure of AM1 was confirmed by single-crystal X-ray diffraction studies and crystallized in a monoclinic crystal system with a P21/c space group, and it shows numerous noncovalent interactions in the crystal packing. The high sensitivity of AM1 to Hg(2+) ions was imputed to the quenching mechanism and was estimated by Fourier transform infrared (FT-IR) spectroscopy, nuclear magnetic resonance ((1)H-NMR), high-resolution mass spectrometry (HRMS), ultraviolet–visible (UV–vis) absorbance, fluorescence (FL) emission, Job’s plot, B-H plot, and DFT calculation. Naked eye color change of AM1 solution to yellow and turn-off FL by the addition of mercury ion is due to complex formation. In addition to mercury ions, the sensor displayed a new absorption peak at around 240 nm. Furthermore, an AM1-coated test strip is used as the solid support sensor, and real-time detection of Hg(2+) ions in the HeLa cell line by fluorescence microscopy is performed. |
format | Online Article Text |
id | pubmed-9301703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93017032022-07-22 Thiazole-Formulated Azomethine Compound for Three-Way Detection of Mercury Ions in Aqueous Media and Application in Living Cells Umabharathi, Pushparani Selvakumar Karpagam, Subramanian ACS Omega [Image: see text] Heavy metal ions are extremely poisonous and cause long-term harm to living organisms. Among these ions, mercury is the most toxic metal and has no notorious purpose in the human body. In this regard, an elegant azomethine thiazole compound AM1 was synthesized, and it was found to be highly sensitive to three-way detection of mercury ions with detection limits of 0.1126 × 10(–9) M (FL) and 0.64 × 10(–6) M (UV–vis). AM1 highlighted the capability to detect mercury ions through the colorimetric method, the fluorometric method, and via the naked eye in three-way detection. In addition, the structure of AM1 was confirmed by single-crystal X-ray diffraction studies and crystallized in a monoclinic crystal system with a P21/c space group, and it shows numerous noncovalent interactions in the crystal packing. The high sensitivity of AM1 to Hg(2+) ions was imputed to the quenching mechanism and was estimated by Fourier transform infrared (FT-IR) spectroscopy, nuclear magnetic resonance ((1)H-NMR), high-resolution mass spectrometry (HRMS), ultraviolet–visible (UV–vis) absorbance, fluorescence (FL) emission, Job’s plot, B-H plot, and DFT calculation. Naked eye color change of AM1 solution to yellow and turn-off FL by the addition of mercury ion is due to complex formation. In addition to mercury ions, the sensor displayed a new absorption peak at around 240 nm. Furthermore, an AM1-coated test strip is used as the solid support sensor, and real-time detection of Hg(2+) ions in the HeLa cell line by fluorescence microscopy is performed. American Chemical Society 2022-07-04 /pmc/articles/PMC9301703/ /pubmed/35874226 http://dx.doi.org/10.1021/acsomega.2c02473 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 | Umabharathi, Pushparani Selvakumar Karpagam, Subramanian Thiazole-Formulated Azomethine Compound for Three-Way Detection of Mercury Ions in Aqueous Media and Application in Living Cells |
title | Thiazole-Formulated Azomethine Compound for Three-Way
Detection of Mercury Ions in Aqueous Media and Application in Living
Cells |
title_full | Thiazole-Formulated Azomethine Compound for Three-Way
Detection of Mercury Ions in Aqueous Media and Application in Living
Cells |
title_fullStr | Thiazole-Formulated Azomethine Compound for Three-Way
Detection of Mercury Ions in Aqueous Media and Application in Living
Cells |
title_full_unstemmed | Thiazole-Formulated Azomethine Compound for Three-Way
Detection of Mercury Ions in Aqueous Media and Application in Living
Cells |
title_short | Thiazole-Formulated Azomethine Compound for Three-Way
Detection of Mercury Ions in Aqueous Media and Application in Living
Cells |
title_sort | thiazole-formulated azomethine compound for three-way
detection of mercury ions in aqueous media and application in living
cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301703/ https://www.ncbi.nlm.nih.gov/pubmed/35874226 http://dx.doi.org/10.1021/acsomega.2c02473 |
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