Designing catalysts for olefin polymerization and copolymerization: beyond electronic and steric tuning

位阻效应 共聚物 聚合 催化作用 烯烃聚合 聚烯烃 材料科学 烯烃纤维 化学 电子效应 聚合物 组合化学 纳米技术 有机化学 图层(电子)
作者
Changle Chen
出处
期刊:Nature Reviews Chemistry [Nature Portfolio]
卷期号:2 (5): 6-14 被引量:657
标识
DOI:10.1038/s41570-018-0003-0
摘要

More than 50 years have passed since Ziegler and Natta shared the Nobel Prize in Chemistry for their discovery of olefin polymerization catalysts. The field of metal-catalysed polymerization has since matured, in no small part owing to the development of several high-performance catalysts. Although polymerization research has in many ways been driven by catalyst development, this has often occurred as a result of trial and error discovery of a promising motif, followed by extensive tuning of the steric and electronic properties of the ligand(s) present in the lead complex. Recently, some alternative design strategies have emerged that afforded new classes of olefin polymerization catalysts. This Perspective highlights recently designed catalyst motifs and the novel reactivity patterns they enable. Special attention is given to methods specifically designed for the copolymerization of ethylene with polar-functionalized co-monomers — challenging reactions that showcase these creatively designed catalyst motifs. The development of high-performance olefin polymerization catalysts is a major driving force in polyolefin studies. This Perspective discusses some alternative strategies for catalyst design — strategies in which existing systems are tuned beyond merely modifying the electronic and steric properties.
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