Zirconium and titanium complexes containing hydrotris(pyrazolyl)borate (Tp) or hydrotris(3,5-dimethylpyrazolyl)borate (Tp*) as a ligand have been examined as polymerization precatalysts for ethylene, propylene and styrene. Activation of the group 4 transition-metal complexes by methylaluminoxane exhibits a greater catalytic activity in ethylene polymerization for TpMCl(3), (M = Zr, Ti) than for the corresponding mono-cyclopentadienyl analogue, CpMCl3. Dimethyl substitution on the pyrazolyl groups enhances the activity for the Zr complex (Tp*ZrCl3,), but not for the Ti complex (Tp*TiCl). Complete substitution of O'Bu or OPh groups for Cl ligands in Tp*ZrCl3, greatly decreases the activity. Mono substitution of an OPh group for one Cl ligand in Tp*TiCl3 does not affect the activity. The addition of propylene comonomer reduces the catalytic activity of Zr complexes containing Tp or Tp* to a considerable degree. The Tp and Tp* complexes of Zr and Ti produce atactic polymers from styrene. (C) 1998 Elsevier Science B.V. All rights reserved.