Polymerization of styrene with supported half-sandwich complexes
✍ Scribed by W. Kaminsky; D. Arrowsmith; C. Strübel
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 163 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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✦ Synopsis
Polymerizations of styrene were carried out with half-sandwich complexes supported on silica, CpTiX 3 /MAO/SiO 2 (X ϭ Cl, F). The optimum values for the polymerization time, the amount of cocatalyst and the Al support /Ti ratio were found for the trichlorinated system. The highest activity obtained was 3,100 g sPS/(mol Ti ϫ h ϫ mol/L styrene). The trihalogenated complexes were compared to one another with respect to their polymerization rate. CpTiCl 3 /MAO/SiO 2 and CpTiF 3 /MAO/SiO 2 behave in a similar manner, suggesting that the active species of both half-sandwich complexes on the support are the same. Furthermore, aging experiments were carried out with CpTiCl 3 /MAO/SiO 2 and, surprisingly, deactivation was observed, as opposed to supported zirconocenes which gain stability against deactivation reactions when anchored to a carrier.
📜 SIMILAR VOLUMES
Ethene was copolymerized with styrene using five different methylalumoxane (MAO) activated half-sandwich complexes of the general formula Me 2 Si(Cp)(N-R)MCl 2 , varying the substituents on the cyclopentadienyl ring and the substituent on the amide (Cp Å tetramethylcyclopentadiene CBT, 1-indenyl IBT
Monocyclopendienyltitanium trichloride (CpTiCl 3 ) was supported on polymer carriers with different hydroxyl contents, and the supported catalysts were used for styrene polymerization. The supported catalysts exhibited high activity even at low Al/Ti ratios and increased the molecular weight of the