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Sulfenate anions as organocatalysts for benzylic chloromethyl coupling polymerization via C=C bond formation
Organocatalytic polymerization reactions have a number of advantages over their metal-catalyzed counterparts, including environmental friendliness, ease of catalyst synthesis and storage, and alternative reaction pathways. Here we introduce an organocatalytic polymerization method called benzylic ch...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931538/ https://www.ncbi.nlm.nih.gov/pubmed/29717123 http://dx.doi.org/10.1038/s41467-018-04095-x |
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author | Li, Minyan Berritt, Simon Wang, Carol Yang, Xiaodong Liu, Yang Sha, Sheng-Chun Wang, Bo Wang, Rui Gao, Xuyu Li, Zhanyong Fan, Xinyuan Tao, Youtian Walsh, Patrick J. |
author_facet | Li, Minyan Berritt, Simon Wang, Carol Yang, Xiaodong Liu, Yang Sha, Sheng-Chun Wang, Bo Wang, Rui Gao, Xuyu Li, Zhanyong Fan, Xinyuan Tao, Youtian Walsh, Patrick J. |
author_sort | Li, Minyan |
collection | PubMed |
description | Organocatalytic polymerization reactions have a number of advantages over their metal-catalyzed counterparts, including environmental friendliness, ease of catalyst synthesis and storage, and alternative reaction pathways. Here we introduce an organocatalytic polymerization method called benzylic chloromethyl-coupling polymerization (BCCP). BCCP is catalyzed by organocatalysts not previously employed in polymerization processes (sulfenate anions), which are generated from bench-stable sulfoxide precatalysts. The sulfenate anion promotes an umpolung polycondensation via step-growth propagation cycles involving sulfoxide intermediates. BCCP represents an example of an organocatalyst that links monomers by C=C double bond formation and offers transition metal-free access to a wide variety of polymers that cannot be synthesized by traditional precursor routes. |
format | Online Article Text |
id | pubmed-5931538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59315382018-05-07 Sulfenate anions as organocatalysts for benzylic chloromethyl coupling polymerization via C=C bond formation Li, Minyan Berritt, Simon Wang, Carol Yang, Xiaodong Liu, Yang Sha, Sheng-Chun Wang, Bo Wang, Rui Gao, Xuyu Li, Zhanyong Fan, Xinyuan Tao, Youtian Walsh, Patrick J. Nat Commun Article Organocatalytic polymerization reactions have a number of advantages over their metal-catalyzed counterparts, including environmental friendliness, ease of catalyst synthesis and storage, and alternative reaction pathways. Here we introduce an organocatalytic polymerization method called benzylic chloromethyl-coupling polymerization (BCCP). BCCP is catalyzed by organocatalysts not previously employed in polymerization processes (sulfenate anions), which are generated from bench-stable sulfoxide precatalysts. The sulfenate anion promotes an umpolung polycondensation via step-growth propagation cycles involving sulfoxide intermediates. BCCP represents an example of an organocatalyst that links monomers by C=C double bond formation and offers transition metal-free access to a wide variety of polymers that cannot be synthesized by traditional precursor routes. Nature Publishing Group UK 2018-05-01 /pmc/articles/PMC5931538/ /pubmed/29717123 http://dx.doi.org/10.1038/s41467-018-04095-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Li, Minyan Berritt, Simon Wang, Carol Yang, Xiaodong Liu, Yang Sha, Sheng-Chun Wang, Bo Wang, Rui Gao, Xuyu Li, Zhanyong Fan, Xinyuan Tao, Youtian Walsh, Patrick J. Sulfenate anions as organocatalysts for benzylic chloromethyl coupling polymerization via C=C bond formation |
title | Sulfenate anions as organocatalysts for benzylic chloromethyl coupling polymerization via C=C bond formation |
title_full | Sulfenate anions as organocatalysts for benzylic chloromethyl coupling polymerization via C=C bond formation |
title_fullStr | Sulfenate anions as organocatalysts for benzylic chloromethyl coupling polymerization via C=C bond formation |
title_full_unstemmed | Sulfenate anions as organocatalysts for benzylic chloromethyl coupling polymerization via C=C bond formation |
title_short | Sulfenate anions as organocatalysts for benzylic chloromethyl coupling polymerization via C=C bond formation |
title_sort | sulfenate anions as organocatalysts for benzylic chloromethyl coupling polymerization via c=c bond formation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931538/ https://www.ncbi.nlm.nih.gov/pubmed/29717123 http://dx.doi.org/10.1038/s41467-018-04095-x |
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