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Polymerization Special Feature: Design of stereoselective Ziegler–Natta propene polymerization catalysts

机译:聚合特性:立体选择性齐格勒-纳塔丙烯聚合催化剂的设计

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摘要

After five decades of largely serendipitous (albeit formidable) progress, catalyst design in Ziegler–Natta olefin polymerization, i.e., the rational implementation of new active species to target predetermined polyolefin architectures, has ultimately become a realistic ambition, thanks to a much deeper fundamental understanding and major advances in the tools of computational chemistry. In this article, we discuss, as a case history, a unique class of stereorigid C2-symmetric bis(phenoxy-amine)Zr(IV) catalysts with controlled kinetic behavior. A large variety of polypropylene microstructures have been obtained with these catalysts by modulating the steric demand of one key substituent, without altering the nature and symmetry of the ancillary ligand framework, under the guidance of computer modeling. This unusual achievement is relevant per se and for the perspective implications in catalyst discovery.
机译:经过数十年的偶然性(尽管是巨大的)进展,齐格勒-纳塔烯烃聚合反应的催化剂设计(即针对预定的聚烯烃结构合理实施新的活性物种)最终由于更深刻的基本理解而成为现实的野心。以及计算化学工具的重大进步。在本文中,我们将作为案例讨论具有可控动力学行为的独特类别的立体刚性C2对称双(苯氧基-胺)Zr(IV)催化剂。在计算机建模的指导下,通过调节一个关键取代基的空间需求,而又不改变辅助配体骨架的性质和对称性,可以用这些催化剂获得各种各样的聚丙烯微结构。这一不寻常的成就本身与催化剂发现中的视角含义相关。

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