Abstract

AbstractThree new titanium complexes bearing salicylidenimine ligands—bis[(salicylidene)‐2,3,5,6‐tetrafluoroanilinato]titanium(IV) dichloride (1), bis[(3,5‐di‐tert‐butylsalicylidene)‐2,3,5,6‐tetrafluoroanilinato]titanium(IV) dichloride (2), and bis[(3,5‐di‐tert‐butylsalicylidene)‐4‐trifluoromethyl‐2,3,5,6‐tetrafluoroanilinato]titanium(IV) dichloride (3)—were synthesized. The catalytic activities of 1–3 for ethylene polymerization were studied with poly(methylaluminoxane) (MAO) as a cocatalyst. Complex 1 was inactive in ethylene polymerization. Complex 2 at a molar ratio of cocatalyst to pre catalyst of AlMAO/Ti = 400–1600 showed very high activity in ethylene polymerization comparable to that of the most efficient metallocene complexes and titanium compounds with phenoxy imine and indolide imine chelating ligands. It gave linear high‐molecular‐weight polyethylene [weight‐average molecular weight (Mw) ≥ 1,700,000. weight‐average molecular weight/number‐average molecular weight (Mw/Mn) = 4–5] with a melting point of 142°C. The ability of the 2/MAO system to copolymerize ethylene with hexene‐1 in toluene was analyzed. No measurable incorporation of the comonomer was observed at 1:1 and 2:1 hexene‐1/ethylene molar ratios. However, the addition of hexene‐1 had a considerable stabilizing effect on the ethylene consumption rate and lowered the melting point of the resultant polymer to 132°C. The 2/MAO system exhibited low activity for propylene polymerization in a medium of the liquid monomer. The polymer that formed was high‐molecular‐weight atactic polypropylene (Mw ∼ 870,000, Mw/Mn = 9–10) showing elastomeric behavior. The activity of 3/MAO in ethylene polymerization was approximately 70 times lower than that of the 2/MAO system. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 95: 1040–1049, 2005

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