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Thiophenium Salts as New Oxidant for Redox Polymerization under Mild- and Low-Toxicity Conditions

In mild conditions (under air, room temperature, no monomer purification and without any energy activation), redox free radical polymerization (RFRP) is considered as one of the most effective methods to polymerize (meth)acrylate monomers. In the past several years, there has been a growing interest...

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Autores principales: Barrat, Alexis, Simon, Frédéric, Mazajczyk, Jérôme, Charriere, Bruno, Fouquay, Stéphane, Lalevee, Jacques
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9861688/
https://www.ncbi.nlm.nih.gov/pubmed/36677685
http://dx.doi.org/10.3390/molecules28020627
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author Barrat, Alexis
Simon, Frédéric
Mazajczyk, Jérôme
Charriere, Bruno
Fouquay, Stéphane
Lalevee, Jacques
author_facet Barrat, Alexis
Simon, Frédéric
Mazajczyk, Jérôme
Charriere, Bruno
Fouquay, Stéphane
Lalevee, Jacques
author_sort Barrat, Alexis
collection PubMed
description In mild conditions (under air, room temperature, no monomer purification and without any energy activation), redox free radical polymerization (RFRP) is considered as one of the most effective methods to polymerize (meth)acrylate monomers. In the past several years, there has been a growing interest in research on the development of new redox initiating systems (RISs), thanks mainly to the evolution of toxicity labeling and the stability issue of the current RIS based on peroxide and aromatic amine. In this study, a new, low-toxicity RIS based on thiophenium salt as the oxidant species is presented with various reductive species. The reactivity and the stability of the proposed RISs are investigated and the synthesis of new thiophenium salts reported.
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spelling pubmed-98616882023-01-22 Thiophenium Salts as New Oxidant for Redox Polymerization under Mild- and Low-Toxicity Conditions Barrat, Alexis Simon, Frédéric Mazajczyk, Jérôme Charriere, Bruno Fouquay, Stéphane Lalevee, Jacques Molecules Article In mild conditions (under air, room temperature, no monomer purification and without any energy activation), redox free radical polymerization (RFRP) is considered as one of the most effective methods to polymerize (meth)acrylate monomers. In the past several years, there has been a growing interest in research on the development of new redox initiating systems (RISs), thanks mainly to the evolution of toxicity labeling and the stability issue of the current RIS based on peroxide and aromatic amine. In this study, a new, low-toxicity RIS based on thiophenium salt as the oxidant species is presented with various reductive species. The reactivity and the stability of the proposed RISs are investigated and the synthesis of new thiophenium salts reported. MDPI 2023-01-07 /pmc/articles/PMC9861688/ /pubmed/36677685 http://dx.doi.org/10.3390/molecules28020627 Text en © 2023 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
Barrat, Alexis
Simon, Frédéric
Mazajczyk, Jérôme
Charriere, Bruno
Fouquay, Stéphane
Lalevee, Jacques
Thiophenium Salts as New Oxidant for Redox Polymerization under Mild- and Low-Toxicity Conditions
title Thiophenium Salts as New Oxidant for Redox Polymerization under Mild- and Low-Toxicity Conditions
title_full Thiophenium Salts as New Oxidant for Redox Polymerization under Mild- and Low-Toxicity Conditions
title_fullStr Thiophenium Salts as New Oxidant for Redox Polymerization under Mild- and Low-Toxicity Conditions
title_full_unstemmed Thiophenium Salts as New Oxidant for Redox Polymerization under Mild- and Low-Toxicity Conditions
title_short Thiophenium Salts as New Oxidant for Redox Polymerization under Mild- and Low-Toxicity Conditions
title_sort thiophenium salts as new oxidant for redox polymerization under mild- and low-toxicity conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9861688/
https://www.ncbi.nlm.nih.gov/pubmed/36677685
http://dx.doi.org/10.3390/molecules28020627
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