首页> 外文期刊>Macromolecules >Homo- and copolymerization of ethylene and α-olefins over 1- and 2-siloxy-substituted ethylenebis(indenyl)zirconium and ethylenebis(tetrahydroindenyl)zirconium dichlorides
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Homo- and copolymerization of ethylene and α-olefins over 1- and 2-siloxy-substituted ethylenebis(indenyl)zirconium and ethylenebis(tetrahydroindenyl)zirconium dichlorides

机译:乙烯和α-烯烃在1-和2-甲氧基取代的亚乙基双(茚基)锆和亚乙基双(四氢茚基)二氯化锆上的均聚和共聚

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摘要

The influence of siloxy substitution of ethylene-bridged bis(indenyl)- and bis(tetrahydroindenyl)zirconium dichlorides on ethylene/α-olefin copolymerization and ethylene homopolymerization performance was investigated. Ethylene was copolymerized with 1-hexene and 1-hexadecene over rac-[ethylenebis(1-(tert-butyldimethylsiloxy)- 3-indenyl)]zirconium dichloride (1), rac-[ethylenebis(1-(tert-butyldimethylsiloxy)-4,5,6, 7-tetrahydro-3-indenyl)]zirconium dichloride (H1), rac-[ethylenebis(2-(tert-butyldimethylsiloxy)- 1-indenyl)]zirconium dichloride (2), and rac-ethylenebis(1-indenyl)zirconium dichloride (EBI) using methylaluminoxane (MAO) as cocatalyst. 1-Siloxy substitution was found to remarkably improve the copolymerization ability and 2-siloxy substitution to enhance the polymerization activity of ethylenebis(indenyl)zirconium dichlorides. Optimum homo- and copolymerization performance was observed at a very low Al(MAO) concentration, which for 2 could be reduced to a level of 0.2 mmol/dm3 by using a small amount of triisobutylaluminum. The 1-siloxy-substituted metallocene catalysts 1 and H1 (hydrogenerated 1) revealed decreasing comonomer incorporation and increasing induction times with increasing Al(MAO) concentration, which indicates the presence of unfavorable interactions between these metallocenes and MAO. Chain termination occurred mainly by chain transfer to the monomer and β-hydrogen transfer to the metal for catalysts with indenyl and tetrahydroindenyl ligands, respectively.
机译:研究了乙烯桥联的双(茚基)-和双(四氢茚基)二氯化锆的甲硅烷氧基取代对乙烯/α-烯烃共聚和乙烯均聚性能的影响。将乙烯与1-己烯和1-十六烯在外消旋-[亚乙基双(1-(叔丁基二甲基甲硅烷氧基)-3-茚基)]二氯化锆(1),外消旋-[亚乙基双(1-(叔丁基二甲基甲硅烷氧基)-4]上共聚,5,6,7-四氢-3-茚基)]二氯化锆(H1),rac- [亚乙基双(2-(叔丁基二甲基甲硅烷氧基)-1-茚基)]二氯化锆(2)和rac-亚乙基双(1 -茚基)二氯化锆(EBI),使用甲基铝氧烷(MAO)作为助催化剂。发现1-甲硅烷氧基取代显着提高了共聚能力,而2-甲硅烷氧基取代增强了二氯化亚乙基双(茚基)锆的聚合活性。在非常低的Al(MAO)浓度下,观察到最佳的均相和共聚性能,通过使用少量的三异丁基铝可以将2降低到0.2 mmol / dm3的水平。 1-甲硅烷氧基取代的茂金属催化剂1和H1(氢化生成1)显示出随着Al(MAO)浓度的增加,共聚单体的结合减少,诱导时间增加,这表明这些茂金属与MAO之间存在不利的相互作用。对于具有茚基和四氢茚基配体的催化剂,链终止主要通过链转移至单体和β-氢转移至金属而发生。

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