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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...

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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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
Descripción
Sumario: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.