首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Propylene polymerization to high molecular weight atactic polypropylene and copolymerization with 1-hexene using monocyclopentadienyl titanium catalysts
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Propylene polymerization to high molecular weight atactic polypropylene and copolymerization with 1-hexene using monocyclopentadienyl titanium catalysts

机译:丙烯聚合为高分子量无规聚丙烯,并使用单环戊二烯基钛催化剂与1-己烯共聚

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摘要

A number of cyclopentadienyltitanium aryloxide complexes, 1-Ar-2,3,4,5-Me-4-Cp(2,6-(Pr2C6H3O)-Pr-i)TiCl2 (Ar = 4-Me(3)SiPhenyl (5), 4-(i)PrPhenyl ( 6), 4-MePhenyl (7), 3,5-(CF3)(2)Phenyl (8)) and (1-Ar-2,3,4,5-Me4CpTiCl2) 2(OAr'O) (Ar' = 4,4'-(3,3',5,5'-(Pr4C6H2)-Pr-i-C6H2), Ar = 4-SiMe(3)Phenyl ( 9), 4-MePhenyl (10)) were synthesized from the reaction of a corresponding cyclopentadienyl titanium trichloride derivative with the lithium salt of a relevant phenol. The molecular structures of complexes 6, 7 and 8 were determined by X-ray crystallography. Upon activation with (Bu3Al)-Bu-i and Ph3CB(C6F5)(4), all mononuclear complexes 5- 8 exhibit good catalytic activities for propylene polymerization, whereas the binuclear complexes 9 and 10 show lower catalytic activities under the same polymerization conditions. C-13 NMR, DSC and GPC analysis indicates the produced polymers are atactic polypropylene with relatively high molecular weight. It was found that the substituents on both the cyclopentadienyl and aryloxy ligands of these complexes show obvious influence on the molecular weight of the resultant polymers with complex 5 producing the highest molecular weight atactic polypropylene. Complexes 5, 6 and 7 were also tested as catalysts for copolymerization of propylene with 1-hexene and copolymers with 1.2-10.1% comonomer incorporation were obtained in reasonable catalytic activity.
机译:许多环戊二烯基钛的芳氧化物配合物1-Ar-2,3,4,5-Me-4-Cp(2,6-(Pr2C6H3O)-Pr-i)TiCl2(Ar = 4-Me(3)SiPhenyl(5 ),4-(i)PrPhenyl(6),4-MePhenyl(7),3,5-(CF3)(2)Phenyl(8))和(1-Ar-2,3,4,5-Me4CpTiCl2) 2(OAr'O)(Ar'= 4,4'-(3,3',5,5'-(Pr4C6H2)-Pr-1-C6H2),Ar = 4-SiMe(3)苯基(9),由相应的环戊二烯基三氯化钛衍生物与有关酚的锂盐反应合成了4-MePhenyl(10)。配合物6、7和8的分子结构通过X射线晶体学测定。在用(Bu3Al)-Bu-i和Ph3CB(C6F5)(4)活化后,所有单核络合物5-8均表现出良好的丙烯聚合催化活性,而双核络合物9和10在相同聚合条件下显示出较低的催化活性。 C-13 NMR,DSC和GPC分析表明,所得聚合物为分子量较高的无规立构聚丙烯。已发现这些配合物的环戊二烯基和芳氧基配体上的取代基对所得聚合物的分子量显示出明显的影响,配合物5产生最高分子量的无规聚丙烯。还测试了配合物5、6和7作为丙烯与1-己烯共聚的催化剂,并以合理的催化活性获得了掺入1.2-10.1%共聚单体的共聚物。

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