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利用环状酯和醚开环聚合中的多金属协同作用

Exploiting Multimetallic Cooperativity in the Ring-Opening Polymerization of Cyclic Esters and Ethers.

作者信息

Yolsal Utku, Shaw Peter J, Lowy Phoebe A, Chambenahalli Raju, Garden Jennifer A

机构信息

School of Chemistry, University of Edinburgh, Joseph Black Building, David Brewster Road, Edinburgh, EH9 3FJ, United Kingdom.

出版信息

ACS Catal. 2024 Jan 8;14(2):1050-1074. doi: 10.1021/acscatal.3c05103. eCollection 2024 Jan 19.

Abstract

The use of multimetallic complexes is a rapidly advancing route to enhance catalyst performance in the ring-opening polymerization of cyclic esters and ethers. Multimetallic catalysts often outperform their monometallic analogues in terms of reactivity and/or polymerization control, and these improvements are typically attributed to "multimetallic cooperativity". Yet the origins of multimetallic cooperativity often remain unclear. This review explores the key factors underpinning multimetallic cooperativity, including metal-metal distances, the flexibility, electronics and conformation of the ligand framework, and the coordination environment of the metal centers. Emerging trends are discussed to provide insights into why cooperativity occurs and how to harness cooperativity for the development of highly efficient multimetallic catalysts.

摘要

使用多金属配合物是一种迅速发展的途径,可提高环状酯和醚开环聚合反应中的催化剂性能。多金属催化剂在反应活性和/或聚合控制方面通常优于其单金属类似物,这些改进通常归因于“多金属协同作用”。然而,多金属协同作用的起源往往仍不明确。本综述探讨了支撑多金属协同作用的关键因素,包括金属-金属距离、配体骨架的灵活性、电子性质和构象,以及金属中心的配位环境。讨论了新出现的趋势,以深入了解协同作用为何会发生,以及如何利用协同作用来开发高效的多金属催化剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f658/10804381/cee45c8c244f/cs3c05103_0029.jpg

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