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Updated: Jun 9, 2025

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
Published on: November 21, 2017
Efficient synthesis of polycarbonate ether polyol via copolymerization of CO2 and 1,2-butylene oxide over a layered
Chen Liu1,2, Yan Cao1, Xianqiang Zeng1
1CAS Key Laboratory of Green Process and Engineering, National Engineering Research Center of Green Recycling for Strategic Metal Resources, Institute of Process Engineering, Chinese Academy of Sciences Beijing 100190 China lgwang@ipe.ac.cn.
Abstract:
Polycarbonate ether polyol synthesized by the copolymerization of carbon dioxide (CO2) and epoxides is a promising technology for chemically fixing CO2 and manufacturing degradable polymeric materials. However, research on the copolymerization of CO2 and 1,2-butylene oxide (BO) to produce polycarbonate ether polyol is relatively scarce. Herein, we employed layered Zn-Co double metal cyanide (L-DMC) as a catalyst for the copolymerization of CO2 and BO to obtain polycarbonate ether polyol. Under optimized conditions, the L-DMC-mediated copolymerization of CO2 and BO displays excellent activity (catalytic productivity up to 1500 g polymer per g catalyst) and a high CO2 incorporation fraction in polycarbonate ether polyol rate of 35.5%. In situ FTIR spectroscopy experiments showed a short induction period (10 min) in polymerization and competition between the synthesized polycarbonate ether polyol and butylene carbonate (BC). The properties of easy preparation, stability, and excellent catalytic performance of L-DMC suggest that it may be a promising candidate for large-scale production of CO2-BO-based polymers.
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