Fluorinated bis(phenoxy-imine) Ti complexes with MAO: Remarkable catalysts for living ethylene and syndioselective living propylene polymerization

被引:87
作者
Furuyama, R [1 ]
Saito, J [1 ]
Ishii, S [1 ]
Makio, H [1 ]
Mitani, M [1 ]
Tanaka, H [1 ]
Fujita, T [1 ]
机构
[1] Mitsui Chem Inc, R&D Ctr, Chiba 2990265, Japan
关键词
olefin polymerization; non-metallocene; living polymerization; FI catalysts; syndiotactic polypropylene; block copolymers;
D O I
10.1016/j.jorganchem.2005.03.060
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Based on new results as well as the reported data, the ethylene and propylene polymerization behavior of bis(phenoxy-imine) Ti complexes (Ti-FI Catalysts) combined with MAO (particularly that of their fluorinated versions) is discussed, with an emphasis on the characteristics and mechanisms of living ethylene and syndioselective living propylene polymerization. Unlike common living olefin polymerization catalysts, fluorinated Ti-FI Catalysts with MAO display thermally robust living behavior and polymerize ethylene in a highly controlled manner at temperatures as high as 50 degrees C. Additionally, despite being C-2-symmetric catalysts, fluorinated Ti-FI Catalysts/MAO mediate highly syndioselective living propylene polymerization. Fluorinated Ti-FI Catalysts that we developed are the first examples of catalysts that induce the living polymerization of both ethylene and propylene. In addition, they are also the first examples of living and, at the same time, highly stereoselective propylene polymerization catalysts. The versatile and robust living nature of the fluorinated Ti-FI Catalysts allows the preparation of a wide variety of unique living polymers; some of which can even be produced catalytically. On the basis of theoretical calculations as well as experimental results, we conclude that these unusual polymerization features of fluorinated Ti-FI Catalysts originate from an attractive interaction between the ligand and a growing polymer chain and/or the fluxional character of the catalyst coupled with 2,1-regiochemistry. This is in stark contrast to group 4 metallocene catalysts, which control olefin polymerization mainly by repulsive interactions based on the rigidly organized ligand frameworks. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:4398 / 4413
页数:16
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