The polymerization of norbornene with two new families of late transition metal-based catalysts derived from: (i) Ni and Pd complexes bearing bulky diammine ligands, with the general formula [ArN=C(R)-C(R)=NAr]MeX 2 and (ii) Fe and Co complexes bearing bulky arylimine ligands with the general formula [(2,6-ArN=C(Me)) 2 C 5 H 3 N]MX 2 is reported. New Co-based complexes have been tested as well. A prevailingly vinylic, amorphous polymer was obtained with all the catalysts tested, whose solubility in organic solvents is substantially dependent on the molucular weight. Polymerization activity greatly varies from one catalyst to another and depends rather on the metal than on the ligand. Solvent polarity and temperature greatly affect the polymerization yields. Besides a dramatic reduction of molecular weights, the addition of small amounts of 1-hexene produces a noticeable increase in the catalytic activity. NMR analysis shows that in all cases a certain percentage of ROMP polymer is present and that, in general, the variations in polymerization conditions, which produce an increase in activity, simultaneously affect a reduction of the ROMP percentage.