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Beyond Traditional RAFT: Alternative Activation of Thiocarbonylthio Compounds for Controlled Polymerization
Recent developments in polymerization reactions utilizing thiocarbonylthio compounds have highlighted the surprising versatility of these unique molecules. The increasing popularity of reversible addition–fragmentation chain transfer (RAFT) radical polymerization as a means of producing well‐defined...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039976/ https://www.ncbi.nlm.nih.gov/pubmed/27711266 http://dx.doi.org/10.1002/advs.201500394 |
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author | McKenzie, Thomas G. Fu, Qiang Uchiyama, Mineto Satoh, Kotaro Xu, Jiangtao Boyer, Cyrille Kamigaito, Masami Qiao, Greg G. |
author_facet | McKenzie, Thomas G. Fu, Qiang Uchiyama, Mineto Satoh, Kotaro Xu, Jiangtao Boyer, Cyrille Kamigaito, Masami Qiao, Greg G. |
author_sort | McKenzie, Thomas G. |
collection | PubMed |
description | Recent developments in polymerization reactions utilizing thiocarbonylthio compounds have highlighted the surprising versatility of these unique molecules. The increasing popularity of reversible addition–fragmentation chain transfer (RAFT) radical polymerization as a means of producing well‐defined, ‘controlled’ synthetic polymers is largely due to its simplicity of implementation and the availability of a wide range of compatible reagents. However, novel modes of thiocarbonylthio activation can expand the technique beyond the traditional system (i.e., employing a free radical initiator) pushing the applicability and use of thiocarbonylthio compounds even further than previously assumed. The primary advances seen in recent years are a revival in the direct photoactivation of thiocarbonylthio compounds, their activation via photoredox catalysis, and their use in cationic polymerizations. These synthetic approaches and their implications for the synthesis of controlled polymers represent a significant advance in polymer science, with potentially unforeseen benefits and possibilities for further developments still ahead. This Research News aims to highlight key works in this area while also clarifying the differences and similarities of each system. |
format | Online Article Text |
id | pubmed-5039976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50399762016-10-03 Beyond Traditional RAFT: Alternative Activation of Thiocarbonylthio Compounds for Controlled Polymerization McKenzie, Thomas G. Fu, Qiang Uchiyama, Mineto Satoh, Kotaro Xu, Jiangtao Boyer, Cyrille Kamigaito, Masami Qiao, Greg G. Adv Sci (Weinh) Research News Recent developments in polymerization reactions utilizing thiocarbonylthio compounds have highlighted the surprising versatility of these unique molecules. The increasing popularity of reversible addition–fragmentation chain transfer (RAFT) radical polymerization as a means of producing well‐defined, ‘controlled’ synthetic polymers is largely due to its simplicity of implementation and the availability of a wide range of compatible reagents. However, novel modes of thiocarbonylthio activation can expand the technique beyond the traditional system (i.e., employing a free radical initiator) pushing the applicability and use of thiocarbonylthio compounds even further than previously assumed. The primary advances seen in recent years are a revival in the direct photoactivation of thiocarbonylthio compounds, their activation via photoredox catalysis, and their use in cationic polymerizations. These synthetic approaches and their implications for the synthesis of controlled polymers represent a significant advance in polymer science, with potentially unforeseen benefits and possibilities for further developments still ahead. This Research News aims to highlight key works in this area while also clarifying the differences and similarities of each system. John Wiley and Sons Inc. 2016-05-17 /pmc/articles/PMC5039976/ /pubmed/27711266 http://dx.doi.org/10.1002/advs.201500394 Text en © 2016 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research News McKenzie, Thomas G. Fu, Qiang Uchiyama, Mineto Satoh, Kotaro Xu, Jiangtao Boyer, Cyrille Kamigaito, Masami Qiao, Greg G. Beyond Traditional RAFT: Alternative Activation of Thiocarbonylthio Compounds for Controlled Polymerization |
title | Beyond Traditional RAFT: Alternative Activation of Thiocarbonylthio Compounds for Controlled Polymerization |
title_full | Beyond Traditional RAFT: Alternative Activation of Thiocarbonylthio Compounds for Controlled Polymerization |
title_fullStr | Beyond Traditional RAFT: Alternative Activation of Thiocarbonylthio Compounds for Controlled Polymerization |
title_full_unstemmed | Beyond Traditional RAFT: Alternative Activation of Thiocarbonylthio Compounds for Controlled Polymerization |
title_short | Beyond Traditional RAFT: Alternative Activation of Thiocarbonylthio Compounds for Controlled Polymerization |
title_sort | beyond traditional raft: alternative activation of thiocarbonylthio compounds for controlled polymerization |
topic | Research News |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039976/ https://www.ncbi.nlm.nih.gov/pubmed/27711266 http://dx.doi.org/10.1002/advs.201500394 |
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