

FOLLOWUS
Ministry of Education Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science
Xing-Hong Zhang, E-mail xhzhang@zju.edu.cn
Received:30 August 2017,
Accepted:21 September 2017,
Online First:21 November 2017,
Published:05 February 2018
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Yang Li, Ying-Ying Zhang, Bin Liu, et al. HCAⅡ-inspired Catalysts for Making Carbon Dioxide-based Copolymers: The Role of Metal-hydroxide Bond[J]. Chinese Journal of Polymer Science, 2018, 36(2): 139-148.
Yang Li, Ying-Ying Zhang, Bin Liu, et al. HCAⅡ-inspired Catalysts for Making Carbon Dioxide-based Copolymers: The Role of Metal-hydroxide Bond[J]. Chinese Journal of Polymer Science, 2018, 36(2): 139-148. DOI: 10.1007/s10118-018-2047-5.
The general characteristics of the active center of the catalysts (including zinc-cobalt(Ⅲ) double metal cyanide complex [Zn-Co(Ⅲ) DMCC]) for the copolymerization reaction of carbon dioxide (CO
2
) with epoxide are summarized. By comparing the active center
catalytic performance of the Zn-Co(Ⅲ) DMCC (and other catalysts) with HCAII enzyme in the organism for activating CO
2
(COS and CS
2
)
we proposed that the metal-hydroxide bond (M-OH)
which is the real catalytic center of human carbonic anhydride II (HCAII)
is also the catalytic (initiating) center for the copolymerization. It accelerates the copolymerization and forms a closed catalytic cycle through the chain transfer reaction to water (and thus strictly meets the definition of the catalyst). In addition
the metal-hydroxide bond catalysis could well explain the oxygen/sulfur exchange reaction (O/S ER) in metal (Zn
Cr)-catalyzed copolymerization of COS (and CS
2
) with epoxides. Therefore
it is very promising to learn from HCAII enzyme to develop biomimetic catalyst for highly active CO
2
/epoxide copolymerization in a well-controlled manner under mild conditions.
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