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环氧化物与一氧化碳共聚物的演变:催化剂、单体、结构及应用

Evolution of Copolymers of Epoxides and CO: Catalysts, Monomers, Architectures, and Applications.

作者信息

Yang Guan-Wen, Xie Rui, Zhang Yao-Yao, Xu Cheng-Kai, Wu Guang-Peng

机构信息

MOE Laboratory of Macromolecular Synthesis and Functionalization, Key Laboratory of Adsorption and Separation Materials & Technologies of Zhejiang Province, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310058, Zhejiang, China.

National Engineering Laboratory for Textile Fiber Materials and Processing Technology, School of Materials Science and Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, Zhejiang, China.

出版信息

Chem Rev. 2024 Nov 13;124(21):12305-12380. doi: 10.1021/acs.chemrev.4c00517. Epub 2024 Oct 25.

Abstract

The copolymerization of CO and epoxides presents a transformative approach to converting greenhouse gases into aliphatic polycarbonates (CO-PCs), thereby reducing the polymer industry's dependence on fossil resources. Over the past 50 years, a wide array of metallic catalysts, both heterogeneous and homogeneous, have been developed to achieve precise control over polymer selectivity, sequence, regio-, and stereoselectivity. This review details the evolution of metal-based catalysts, with a particular focus on the emergence of organoborane catalysts, and explores how these catalysts effectively address kinetic and thermodynamic challenges in CO/epoxides copolymerization. Advances in the synthesis of CO-PCs with varied sequence and chain architectures through diverse polymerization protocols are examined, alongside the applications of functional CO-PCs produced by incorporating different epoxides. The review also underscores the contributions of computational techniques to our understanding of copolymerization mechanisms and highlights recent advances in the closed-loop chemical recycling of CO-sourced polycarbonates. Finally, the industrialization efforts of CO-PCs are discussed, offering readers a comprehensive understanding of the evolution and future potential of epoxide copolymerization with CO.

摘要

一氧化碳(CO)与环氧化物的共聚反应为将温室气体转化为脂肪族聚碳酸酯(CO-PCs)提供了一种变革性方法,从而降低聚合物行业对化石资源的依赖。在过去50年里,人们开发了各种各样的金属催化剂,包括多相和均相催化剂,以实现对聚合物选择性、序列、区域和立体选择性的精确控制。本综述详细介绍了金属基催化剂的发展历程,特别关注有机硼烷催化剂的出现,并探讨了这些催化剂如何有效应对CO/环氧化物共聚反应中的动力学和热力学挑战。通过不同的聚合方案合成具有不同序列和链结构的CO-PCs的进展进行了研究,同时还探讨了通过引入不同环氧化物制备的功能性CO-PCs的应用。该综述还强调了计算技术对我们理解共聚反应机理的贡献,并突出了源自CO的聚碳酸酯闭环化学回收的最新进展。最后,讨论了CO-PCs的工业化努力,使读者全面了解环氧化物与CO共聚反应的发展历程和未来潜力。

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