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Cooperative Recognition of Ni(2+) Triggered by Fluoride Ions in Naturally Occurring α-Hydroxyquinone Derivatives
[Image: see text] Perezone is a naturally occurring hydroxyquinone that has been deeply studied from different chemical aspects, such as therapeutics, electrochemistry, physical–chemical properties, or synthetic approaches that turn it an attractive template for new semisynthetic derivatives with a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246452/ https://www.ncbi.nlm.nih.gov/pubmed/34235313 http://dx.doi.org/10.1021/acsomega.1c01420 |
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author | Valle-Sánchez, Mario Contreras-Celedón, Claudia A. Ochoa-Terán, Adrián Chacón-García, Luis |
author_facet | Valle-Sánchez, Mario Contreras-Celedón, Claudia A. Ochoa-Terán, Adrián Chacón-García, Luis |
author_sort | Valle-Sánchez, Mario |
collection | PubMed |
description | [Image: see text] Perezone is a naturally occurring hydroxyquinone that has been deeply studied from different chemical aspects, such as therapeutics, electrochemistry, physical–chemical properties, or synthetic approaches that turn it an attractive template for new semisynthetic derivatives with a wide range of purposes. Herein, we describe a facile synthetic pathway to obtain new perezone derivatives by the addition of a pyrrole moiety that can be used for ion recognition. Compounds 2–4 showed the capability to interact with several anions and M(2+) cations as separate events that result in colorimetric changes. Moreover, the compounds can behave as heteroditopic receptors. Besides, a previous interaction between fluoride ions and perezone derivatives triggered a successful recognition of M(2+) ions, remarking Ni(2+) as the most interesting phenomenon. These results project the compounds as potential colorimetric receptors for nickel ions in complex solutions. |
format | Online Article Text |
id | pubmed-8246452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82464522021-07-06 Cooperative Recognition of Ni(2+) Triggered by Fluoride Ions in Naturally Occurring α-Hydroxyquinone Derivatives Valle-Sánchez, Mario Contreras-Celedón, Claudia A. Ochoa-Terán, Adrián Chacón-García, Luis ACS Omega [Image: see text] Perezone is a naturally occurring hydroxyquinone that has been deeply studied from different chemical aspects, such as therapeutics, electrochemistry, physical–chemical properties, or synthetic approaches that turn it an attractive template for new semisynthetic derivatives with a wide range of purposes. Herein, we describe a facile synthetic pathway to obtain new perezone derivatives by the addition of a pyrrole moiety that can be used for ion recognition. Compounds 2–4 showed the capability to interact with several anions and M(2+) cations as separate events that result in colorimetric changes. Moreover, the compounds can behave as heteroditopic receptors. Besides, a previous interaction between fluoride ions and perezone derivatives triggered a successful recognition of M(2+) ions, remarking Ni(2+) as the most interesting phenomenon. These results project the compounds as potential colorimetric receptors for nickel ions in complex solutions. American Chemical Society 2021-06-17 /pmc/articles/PMC8246452/ /pubmed/34235313 http://dx.doi.org/10.1021/acsomega.1c01420 Text en © 2021 The Authors. Published by American Chemical Society 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 | Valle-Sánchez, Mario Contreras-Celedón, Claudia A. Ochoa-Terán, Adrián Chacón-García, Luis Cooperative Recognition of Ni(2+) Triggered by Fluoride Ions in Naturally Occurring α-Hydroxyquinone Derivatives |
title | Cooperative Recognition of Ni(2+) Triggered
by Fluoride Ions in Naturally Occurring α-Hydroxyquinone
Derivatives |
title_full | Cooperative Recognition of Ni(2+) Triggered
by Fluoride Ions in Naturally Occurring α-Hydroxyquinone
Derivatives |
title_fullStr | Cooperative Recognition of Ni(2+) Triggered
by Fluoride Ions in Naturally Occurring α-Hydroxyquinone
Derivatives |
title_full_unstemmed | Cooperative Recognition of Ni(2+) Triggered
by Fluoride Ions in Naturally Occurring α-Hydroxyquinone
Derivatives |
title_short | Cooperative Recognition of Ni(2+) Triggered
by Fluoride Ions in Naturally Occurring α-Hydroxyquinone
Derivatives |
title_sort | cooperative recognition of ni(2+) triggered
by fluoride ions in naturally occurring α-hydroxyquinone
derivatives |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246452/ https://www.ncbi.nlm.nih.gov/pubmed/34235313 http://dx.doi.org/10.1021/acsomega.1c01420 |
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