Abstract
Ethylene polymerization studies have been carried out with novel precatalysts of the type: [(η5-C13 H8)-X(t-BuOC6H12)Me-(η5- C5H4)]ZrCl2 [X=C [1a], Si [2a]], [(η5-C13H8)-XMe2- (η5-(t-BuOC6H12C5 H3))] ZrCl2 [X=C [3a], Si [4a]] in the presence of excess methylalumoxane (MAO) to compare their catalytic activity and to delineate the effect of the 6-t-butoxyhexyl functionality on ethylene polymerization. The precatalysts [1a] and [2a] with the bridge functionality showed higher activity in ethylene polymerization than the corresponding complexes [3a] and [4a] which have it on the Cp ring moiety. On the other hand the silyl bridged complexes [2a] and [4a] produced a higher molecular weight polyethylene than the carbon-bridged one, regardless of the location of functional group.
| Original language | English |
|---|---|
| Pages (from-to) | 214-223 |
| Number of pages | 10 |
| Journal | Journal of Organometallic Chemistry |
| Volume | 689 |
| Issue number | 1 |
| DOIs | |
| State | Published - 5 Jan 2004 |
Keywords
- 6-t-Butoxyhexyl pendant
- Ansa-zirconocene
- Ethylene polymerization
- Fluorenyl
- MAO