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Bimetallic Zirconium Amine Bis(phenolate) Polymerization Catalysts: Enhanced Activity and Tacticity Control for Polyolefin Synthesis

机译:双金属锆胺双酚盐聚合催化剂:聚烯烃合成的活性和立构规整度得到控制

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摘要

Binucleating multidentate amine bis(phenolate) ligands with rigid terphenyl backbones were designed to support two zirconium centers locked in close proximity. Polymerizations of propylene or 1-hexene with the synthesized bimetallic precatalysts resulted in polymers with significantly higher isotacticity (up to 79% mmmm) in comparison to the stereoirregular polymers produced with previously reported C_s-symmetric monometallic analogues. The bimetallic precatalysts also display higher activity (up to 124 kg of poly(1-hexene) (mmol of Zr)^(−1) h^(–1)), in comparison to the monometallic analogues, and among the highest activities reported for nonmetallocene catalysts. The stereocontrol is consistent with a bimetallic mechanism involving remote steric interactions with the ligand sphere of the second metal center.
机译:具有刚性三联苯骨架的双核多齿胺双(酚酸酯)配体被设计为支撑两个紧密锁定的锆中心。与用先前报道的C_s-对称单金属类似物生产的立体不规则聚合物相比,丙烯或1-己烯与合成的双金属预催化剂的聚合反应产生的全同立构规整度更高(高达79%mmmm)的聚合物。与单金属类似物相比,双金属预催化剂还显示出更高的活性(高达124千克的聚(1-己烯)(Zr的毫摩尔数)^(-1)h ^(-1)),并且是报道的最高活性用于非茂金属催化剂。立体控制与涉及与第二金属中心的配体球体的远程空间相互作用的双金​​属机理一致。

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