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Direct Copolymerization of CO(2) and Diols

Direct polymerization of CO(2) and diols is promising as a simple and environmental-benign method in place of conventional processes using high-cost and/or hazardous reagents such as phosgene, carbon monoxide and epoxides, however, there are no reports on the direct method due to the inertness of CO...

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Detalles Bibliográficos
Autores principales: Tamura, Masazumi, Ito, Kazuki, Honda, Masayoshi, Nakagawa, Yoshinao, Sugimoto, Hiroshi, Tomishige, Keiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831014/
https://www.ncbi.nlm.nih.gov/pubmed/27075987
http://dx.doi.org/10.1038/srep24038
Descripción
Sumario:Direct polymerization of CO(2) and diols is promising as a simple and environmental-benign method in place of conventional processes using high-cost and/or hazardous reagents such as phosgene, carbon monoxide and epoxides, however, there are no reports on the direct method due to the inertness of CO(2) and severe equilibrium limitation of the reaction. Herein, we firstly substantiate the direct copolymerization of CO(2) and diols using CeO(2) catalyst and 2-cyanopyridine promotor, providing the alternating cooligomers in high diol-based yield (up to 99%) and selectivity (up to >99%). This catalyst system is applicable to various diols including linear C4-C10 α,ω-diols to provide high yields of the corresponding cooligomers, which cannot be obtained by well-known methods such as copolymerization of CO(2) and cyclic ethers and ring-opening polymerization of cyclic carbonates. This process provides us a facile synthesis method for versatile polycarbonates from various diols and CO(2) owing to simplicity of diols modification.