We discovered that the catalysts have vastly different, yet interesting, effects on ethylene/1-octene (EO) and ethylene/styrene (ES) copolymerizations. For ethylene/1-octene copolymers, the activity of the supported catalysts and the amount of 1-octene incorporated into the copolymer is dependent upon the substituents on the cyclopentadienyl ring. The formation of EO copolymers using supported aryloxy-based cyclopentadienyl complexes can also be used as additional evidence for the presence of the tethered aryloxy moiety. The copolymer composition and the thermal properties of these copolymers were also studied.
Ethylene/styrene copolymerizations produced polymers with varying characteristics specific to the catalyst employed for the polymerizations. Polymers synthesized with the supported CpTiCl3 and TMSCpTiCl3 displayed both polyethylene and syndiotactic polystyrene melting points. Conversely, polymers synthesized with the supported Cp*TiCl3 displayed only a polyethylene melting point, while polymers prepared with the supported (TMS)2CpTiCl3 displayed only a syndiotactic polystyrene melting point. These findings suggest that copolymerization of ethylene and styrene is not possible with these catalysts. Analysis of the homopolymerizations of styrene and ethylene with Cp*TiCl3 and (TMS)2CpTiCl3, respectively, shows significantly lower activities, leading to preferential polymerization of the more active monomer during copolymerization.