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Diaryliodonium salts facilitate metal-free mechanoredox free radical polymerizations
Mechanically-induced redox processes offer a promising alternative to more conventional thermal and photochemical synthetic methods. For macromolecule synthesis, current methods utilize sensitive transition metal additives and suffer from background reactivity. Alternative methodology will offer exq...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8985515/ https://www.ncbi.nlm.nih.gov/pubmed/35440983 http://dx.doi.org/10.1039/d2sc00313a |
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author | Zeitler, Sarah M. Chakma, Progyateg Golder, Matthew R. |
author_facet | Zeitler, Sarah M. Chakma, Progyateg Golder, Matthew R. |
author_sort | Zeitler, Sarah M. |
collection | PubMed |
description | Mechanically-induced redox processes offer a promising alternative to more conventional thermal and photochemical synthetic methods. For macromolecule synthesis, current methods utilize sensitive transition metal additives and suffer from background reactivity. Alternative methodology will offer exquisite control over these stimuli-induced mechanoredox reactions to couple force with redox-driven chemical transformations. Herein, we present the iodonium-initiated free-radical polymerization of (meth)acrylate monomers under ultrasonic irradiation and ball-milling conditions. We explore the kinetic and structural consequences of these complementary mechanical inputs to access high molecular weight polymers. This methodology will undoubtedly find broad utility across stimuli-controlled polymerization reactions and adaptive material design. |
format | Online Article Text |
id | pubmed-8985515 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-89855152022-04-18 Diaryliodonium salts facilitate metal-free mechanoredox free radical polymerizations Zeitler, Sarah M. Chakma, Progyateg Golder, Matthew R. Chem Sci Chemistry Mechanically-induced redox processes offer a promising alternative to more conventional thermal and photochemical synthetic methods. For macromolecule synthesis, current methods utilize sensitive transition metal additives and suffer from background reactivity. Alternative methodology will offer exquisite control over these stimuli-induced mechanoredox reactions to couple force with redox-driven chemical transformations. Herein, we present the iodonium-initiated free-radical polymerization of (meth)acrylate monomers under ultrasonic irradiation and ball-milling conditions. We explore the kinetic and structural consequences of these complementary mechanical inputs to access high molecular weight polymers. This methodology will undoubtedly find broad utility across stimuli-controlled polymerization reactions and adaptive material design. The Royal Society of Chemistry 2022-03-16 /pmc/articles/PMC8985515/ /pubmed/35440983 http://dx.doi.org/10.1039/d2sc00313a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Zeitler, Sarah M. Chakma, Progyateg Golder, Matthew R. Diaryliodonium salts facilitate metal-free mechanoredox free radical polymerizations |
title | Diaryliodonium salts facilitate metal-free mechanoredox free radical polymerizations |
title_full | Diaryliodonium salts facilitate metal-free mechanoredox free radical polymerizations |
title_fullStr | Diaryliodonium salts facilitate metal-free mechanoredox free radical polymerizations |
title_full_unstemmed | Diaryliodonium salts facilitate metal-free mechanoredox free radical polymerizations |
title_short | Diaryliodonium salts facilitate metal-free mechanoredox free radical polymerizations |
title_sort | diaryliodonium salts facilitate metal-free mechanoredox free radical polymerizations |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8985515/ https://www.ncbi.nlm.nih.gov/pubmed/35440983 http://dx.doi.org/10.1039/d2sc00313a |
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