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Copper-Free Halodediazoniation of Arenediazonium Tetrafluoroborates in Deep Eutectic Solvents-like Mixtures
Deep Eutectic Solvent (DES)-like mixtures, based on glycerol and different halide organic and inorganic salts, are successfully exploited as new media in copper-free halodediazoniation of arenediazonium salts. The reactions are carried out in absence of metal-based catalysts, at room temperature and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8950527/ https://www.ncbi.nlm.nih.gov/pubmed/35335275 http://dx.doi.org/10.3390/molecules27061909 |
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author | Ghigo, Giovanni Bonomo, Matteo Antenucci, Achille Reviglio, Chiara Dughera, Stefano |
author_facet | Ghigo, Giovanni Bonomo, Matteo Antenucci, Achille Reviglio, Chiara Dughera, Stefano |
author_sort | Ghigo, Giovanni |
collection | PubMed |
description | Deep Eutectic Solvent (DES)-like mixtures, based on glycerol and different halide organic and inorganic salts, are successfully exploited as new media in copper-free halodediazoniation of arenediazonium salts. The reactions are carried out in absence of metal-based catalysts, at room temperature and in a short time. Pure target products are obtained without the need for chromatographic separation. The solvents are fully characterized, and a computational study is presented aiming to understand the reaction mechanism. |
format | Online Article Text |
id | pubmed-8950527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89505272022-03-26 Copper-Free Halodediazoniation of Arenediazonium Tetrafluoroborates in Deep Eutectic Solvents-like Mixtures Ghigo, Giovanni Bonomo, Matteo Antenucci, Achille Reviglio, Chiara Dughera, Stefano Molecules Article Deep Eutectic Solvent (DES)-like mixtures, based on glycerol and different halide organic and inorganic salts, are successfully exploited as new media in copper-free halodediazoniation of arenediazonium salts. The reactions are carried out in absence of metal-based catalysts, at room temperature and in a short time. Pure target products are obtained without the need for chromatographic separation. The solvents are fully characterized, and a computational study is presented aiming to understand the reaction mechanism. MDPI 2022-03-15 /pmc/articles/PMC8950527/ /pubmed/35335275 http://dx.doi.org/10.3390/molecules27061909 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ghigo, Giovanni Bonomo, Matteo Antenucci, Achille Reviglio, Chiara Dughera, Stefano Copper-Free Halodediazoniation of Arenediazonium Tetrafluoroborates in Deep Eutectic Solvents-like Mixtures |
title | Copper-Free Halodediazoniation of Arenediazonium Tetrafluoroborates in Deep Eutectic Solvents-like Mixtures |
title_full | Copper-Free Halodediazoniation of Arenediazonium Tetrafluoroborates in Deep Eutectic Solvents-like Mixtures |
title_fullStr | Copper-Free Halodediazoniation of Arenediazonium Tetrafluoroborates in Deep Eutectic Solvents-like Mixtures |
title_full_unstemmed | Copper-Free Halodediazoniation of Arenediazonium Tetrafluoroborates in Deep Eutectic Solvents-like Mixtures |
title_short | Copper-Free Halodediazoniation of Arenediazonium Tetrafluoroborates in Deep Eutectic Solvents-like Mixtures |
title_sort | copper-free halodediazoniation of arenediazonium tetrafluoroborates in deep eutectic solvents-like mixtures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8950527/ https://www.ncbi.nlm.nih.gov/pubmed/35335275 http://dx.doi.org/10.3390/molecules27061909 |
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