Abstract
Copolymerization of vinyl cyclohexane (monomer-1) with styrene was investigated in the presence of the stereospecific complex catalyst TiCl 3 + Al( iso-C 4H 9) 3. Monomer reactivity ratios were r 1 = 0·177 ± 0·051 and r 2 = 2·117 ± 0·370. The monomer unit distributions in the copolymers were estimated by comparison of the i.r.-spectra of copolymers and the isotactic homopolymers using absorption bands at 565 and 1084 cm −1 which correspond to the vibrations of styrene blocks containing ⩾ 5 styrene units and the band at 985 cm −1 characterizing polystyrene crystallinity. The data indicate the tendency towards alternation in the copolymerization. Analysis of the experimental and literature data led to the conclusion that distribution of the units in copolymers of vinyl cyclohexane with α-olefins is determined by the nature of the α-olefin. The following activity series is proposed for α-olefins in their copolymerization with vinyl cyclohexane in the presence of catalytic systems based on titanium salts and organo-aluminium compounds: propylene >; 4-methylpentene-1 >; styrene >; 3-methylbutene-1 ∼ vinyl cyclohexane.
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