Olefin polymerization by cyclopentadienyltris(dimethylamido)titanium(IV) complexes
✍ Scribed by Barrie Rhodes; Marvin D. Rausch; James C. W. Chien
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 121 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0887-624X
No coin nor oath required. For personal study only.
✦ Synopsis
Several titanium(IV) complexes of the type CpЈTi(NMe 2 ) 3 [CpЈ ϭ cyclopentadienyl (1), (dimethylaminoethyl)cyclopentadienyl (2), indenyl (3), and pentamethylcyclopentadienyl (4)] were prepared, and their catalytic properties in the polymerization of ␣-olefins were examined. Complexes 1 and 2 catalyzed the polymerization of ethylene in the presence of methylaluminoxane with a much higher activity than 3 or 4. Complexes 3 and 4 polymerized ethylene with an activity similar to that of CpTiCl 3 (6). The preactivation of 2, 3, or 4 with trimethylaluminum (TMA) resulted in an increase in ethylene polymerization activities. Also, 1 and 2 were successfully used as ethylene/1-hexene copolymerization catalysts, producing polymers with various amounts of 1-hexene incorporation, depending on the amount of 1-hexene in the feed mixture. Complex 1 likewise effectively polymerized styrene with a higher activity and higher syndiospecificity than the other three catalysts. Complexes 3 and 4 polymerized styrene with low syndiospecificity, whereas 2 produced only atactic polystyrene. The preactivation of 3 or 4 with TMA resulted in an increase in styrene polymerization activities and increased the syndiotacticity percentage of the polymers produced.
📜 SIMILAR VOLUMES
## Abstract Summary: Titanium complexes containing a triaryloxoamine ligand, [TiX{(O‐2,4‐R~2~C~6~H~2~‐6‐CH~2~)~3~N}] (R = Me, __t__Bu; X = O__i__Pr, O‐2,6‐__i__Pr~2~C~6~H~3~), exhibited notable catalytic activity for ethylene polymerization in the presence of MAO, especially at temperatures between
## Abstract The mixed‐ligand complexes [Ti~2~(μ‐OR)~2~(OR)~2~(κ^3^‐tbop)~2~] (1a) for R = Me and (1b) R = Et were prepared by the reaction of Ti(OR)~4~ and H~2~tbop {H~2~tbop = 2,2′‐thiobis[4‐(1,1,3,3‐tetramethylbutyl)phenol]} in methanol. Treatment of 1a and 1b with AlMe~3~ led to the substitution