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首页> 外文期刊>Macromolecular chemistry and physics >Unbridged bicyclic cyclopentadienyl zirconocene complexes: Their possible application as fluxional catalysts in propene polymerization
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Unbridged bicyclic cyclopentadienyl zirconocene complexes: Their possible application as fluxional catalysts in propene polymerization

机译:未桥联的双环环戊二烯基锆茂复合物:在丙烯聚合中作为助熔催化剂的可能应用

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摘要

Three series of novel unbridged bicyclic cyclopentadienyl zirconium complexes, containing six-, seven- and eight-membered saturated rings fused to the cyclopentadienyl unit and bearing different substituents (-H, -CH3, -Ph) in position 2, were used in combination with methylaluminoxane (MAO) for the polymerization of propene at different temperatures. All the catalysts have been shown to be active, the lowest activity being observed with the eight-membered ring systems. with most catalysts the polymers obtained are fully atactic when the polymerizations are conducted at 30degreesC, and become partially isotactic at lower temperatures. The C-13 NMR analysis shows that in one case, that is, when the seven-membered ring is associated with the phenyl substituent in position 2, a a preponderance of the isotactic heptad in the methyl region of C-13 NMR spectrum is observed, which allows us to hypothesize the formation of stereoblocks. [References: 35]
机译:结合使用三组新颖的未桥连双环戊二烯基锆配合物,它们分别与六元,七元和八元饱和环稠合到环戊二烯基单元上,并在位置2带有不同的取代基(-H,-CH3,-Ph)。甲基铝氧烷(MAO)用于在不同温度下聚合丙烯。已显示所有催化剂均具有活性,八元环系统的活性最低。对于大多数催化剂,当聚合反应在30℃下进行时,所得聚合物是完全无规的,而在较低温度下则变为部分等规的。 C-13 NMR分析表明,在一种情况下,即七元环与位置2上的苯基取代基相连时,在C-13 NMR光谱的甲基区域中观察到等规庚烷的优势,这使我们可以假设立体块的形成。 [参考:35]

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