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The catalytic behavior of fluorinated bis(phenoxy−imine)titanium complexes bearing a series of substituents ortho to the phenoxy oxygen was studied for ethylene and ethylene/higher α-olefin (i.e., 1-hexene, 1-octene, and 1-decene) (co)polymerizations. Independent of the magnitude of steric bulk of the ortho -substituent, all the complexes that were investigated produced polyethylenes (PEs) and ethylene/higher α-olefin copolymers with very narrow molecular weight distributions e.g., PEs, M w / M n = 1.05−1.16, M n = 44000−412000; ethylene/1-hexene copolymers, M w / M n = 1.07−1.19, M n = 49000−102000, 1-hexene content 3.2−22.6 mol %, indicative of living polymerization. The incorporation ability for higher α-olefins is highly dependent on the nature of the ortho -substituent, and Ti complexes with a sterically less encumbered ortho -substituent incorporated a higher amount of higher α-olefins. A number of unique block copolymers consisting of highly linear PE and ethylene/1-hexene copolymer segments were prepared using one of the living catalysts with enhanced incorporating capability for higher α-olefins. These block copolymers exhibited lower peak melting temperatures ( T m ) relative to the corresponding homo-PE. The molecular weight and 1-hexene content of the copolymer segment had a considerable effect on the T m values of the resultant block copolymers. A polyethylene- b -poly(ethylene- co -1-hexene) ( M w = 79900, M w / M n = 1.26, 1-hexene content 4.3 mol %) possessed unique tensile properties with a good combination of extensibility and toughness compared to the corresponding blend and random (co)polymers.
Furuyama et al. (Wed,) studied this question.