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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...

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Autores principales: Valle-Sánchez, Mario, Contreras-Celedón, Claudia A., Ochoa-Terán, Adrián, Chacón-García, Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
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.
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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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