Extremozymes-Inspired Catalyst for Epoxide-Based Polymerization

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Authors: Liehang Yang, Shunjie Liu, Hong Chen, Ruoyu Zhang, Zhuo Cd, Xuesi Chen, Xianhong Wang
Cited by: 1
References: 63

Abstract

Enzyme-mimetic catalysis is widely recognized as an effective approach to developing high-performance catalysts. However, in many reactions conducted under conditions far from physiological, designs based on conventional enzymes often limit both activity and robustness. Inspired by hyperthermophilic enzymes that maintain high activity at temperatures nearing 100 °C, we propose an "extremozymes-inspired" design strategy and construct a hexameric aluminum porphyrin catalyst featuring a dimer-of-trimers architecture. By leveraging the geometric constraints imposed by covalent and noncovalent interactions between porphyrins, the catalyst forms two trigonal-pyramidal cavities, thereby replicating both the stable spatial arrangement and the confined multisite catalytic microenvironment characteristic of extremozymes. In propylene oxide (PO) homopolymerization and its copolymerizations with phthalic anhydride (PA) and carbon dioxide (CO2), respectively, the extremozymes-mimetic catalyst achieves record-high turnover frequencies (TOFs) while producing polymers with high number-average molecular weights (Mn) at ppm-level loadings: PO homopolymerization (TOF = 8.1 × 105 h-1, Mn = 1210 kg/mol); PO/PA copolymerization (TOF = 1.4 × 104 h-1, Mn = 140.8 kg/mol); and PO/CO2 copolymerization (TOF = 1.2 × 105 h-1, Mn = 802.3 kg/mol). This study demonstrates the potential of using extremozymes as templates to develop high-performance catalysts and offers new insights into the design of biomimetic catalysts.

Fields of Study & Subjects

biodegradable polymer synthesis and properties Advanced Polymer Synthesis and Characterization Enzyme Catalysis and Immobilization

Publication details

Journal / source
Journal of the American Chemical Society
Publisher
American Chemical Society (ACS)
Volume
148
Issue
30
Pages
32881–32893
Publication date
23 July 2026
Language
EN