Syndiospecific polymerization of styrene catalyzed by half-titanocene catalysts

Those effective catalyst precursors for syndiotactic styrene polymerization, Cp*Ti(OCH(2)-CH=CH(2))(3) (I). Cp*Ti(OCH(2)-CH=CHC(6)H(4))(3) (II), Cp*Ti(OCH(2)C(6)H(5)), (II(1)), Cp*Ti(OCH(2)C(6)H(4)OCH(3))(3) (IV) were synthesized, and the influence of catalyst ligands on the catalytic activity and properties of polymer were investigated. The polymer thus obtained coupled with higher molecular weight and higher syndiotacticity determined by GPC and (13)C NMR as well as solvent extraction manners, respectively. Those catalysts promoted by methyaluminoxane (MAO) as cocatalyst exhibited higher catalytic activity. Of all catalysts mentioned foregoing, Cp*Ti(OCH(2)-CH=CHC(6)H(4))(3) (II), Cp*Ti(OCH(2)C(6)H(5))(3)/MAO (III) and Cp*Ti(OCH(2)C(6)H(4)OCH(3))(3) (IV) catalysts showed higher activity and stability even at fairly low Al/Ti ratio of 600, and possessed excellent control of the stereoregular insertion of monomer, exhibited a significant increase of the ratio of the propagation rates to chain transfer termination. The kinetic and titration results also indicated that those metallocene catalysts (II), (III), and (IV) showed higher catalytic activity and produced polymer with higher molecular weight, because of a great number of active species, and lower ratio of K(tr beta)/K(p), higher ratio of K(tr beta)/K(trs) which indicate that beta-H elimination was predominant. (c) 2005 Elsevier Ltd. All rights reserved.