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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...

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Autores principales: Ghigo, Giovanni, Bonomo, Matteo, Antenucci, Achille, Reviglio, Chiara, Dughera, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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.
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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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