首页> 外文期刊>Organometallics >In Silico Design of C-1- and C-s-Symmetric Fluorenyl-Based Metallocene Catalysts for the Synthesis of High-Molecular-Weight Polymers from Ethylene/Propylene Copolymerization
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In Silico Design of C-1- and C-s-Symmetric Fluorenyl-Based Metallocene Catalysts for the Synthesis of High-Molecular-Weight Polymers from Ethylene/Propylene Copolymerization

机译:用于乙烯/丙烯共聚合合成高分子量聚合物的C-1-和C-s-对称芴基茂金属催化剂的计算机设计

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摘要

C-1- and C-s-symmetric fluorenyl-based metallocenes have been used extensively as catalysts for the synthesis of high-molecular-weight polymers from ethylene and propylene homopolymerization. However, these same catalysts produce only low-molecular-weight polymers in ethylene/propylene copolymerization. We have shown in a recent study that the poor performance of fluorenyl-based C-1-symmetric zirconocenes in ethylene/propylene polymerization is a result of electronic effects. Furthermore, we have also shown in another investigation that incorporating sterically demanding substituents in the 2- and 4- positions of C-2-symmetric zirconocenes can significantly increase molecular weight in copolymerization. In the present study we shall use the same approach (modifying substituents on the cyclopentadienyl and fluorenyl ligands) to design C-1- and C-s-symmetric fluorenyl-based metallocenes that afford high-molecular-weight polymers from ethylene/propylene copolymerization.
机译:C-1-和C-s-对称的芴基金属茂已广泛用作由乙烯和丙烯均聚合成高分子量聚合物的催化剂。然而,这些相同的催化剂在乙烯/丙烯共聚中仅产生低分子量聚合物。我们在最近的研究中表明,芴基的C-1-对称茂锆在乙烯/丙烯聚合中的不良性能是电子效应的结果。此外,我们还在另一项研究中表明,在C-2-对称锆茂金属的2和4位上引入空间上必不可少的取代基可以显着增加共聚分子量。在本研究中,我们将使用相同的方法(修饰环戊二烯基和芴基配体上的取代基)来设计C-1和Cs对称的芴基茂金属,这些化合物可通过乙烯/丙烯共聚获得高分子量的聚合物。

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