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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...

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Detalles Bibliográficos
Autores principales: Zeitler, Sarah M., Chakma, Progyateg, Golder, Matthew R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
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.
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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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