A series of half-sandwich pentamethylcyclopentadienyl chromium(III) complexes bearing a salicylaldiminato ligand, Cp*[2-R1-4-R2-6-(CH
NR3)C6H2O]CrCl [R1 = iPr (1, 4), tBu (2, 3, 5), Ad (6); R2 = H (1, 2, 3), tBu (4, 5, 6); R3 = iPr (1, 2, 5, 6), tBu (3, 4)], were synthesized. All complexes were characterized by elemental analyses and the structures of complexes 1–4 and 6 were determined by X-ray diffraction analysis. These complexes adopt a pseudo-octahedral coordination environment with a three-legged piano stool geometry. Upon activation with a small amount of AlR3, complexes 1–6 all catalyze the polymerization of ethylene in a quasi living fashion with good to high catalytic activity under mild conditions and produce ultra-high molecular weight polyethylene as spherical particles with a diameter of 1–6 mm. The catalytic activity of these complexes and the molecular weight of the produced polyethylene can be tuned in a broad range by changing the R1, R2, and R3groups as well as the AlR3 cocatalyst. It was found that complex 6 with R1 = Ad, R2 = tBu, and R3 = iPr shows the highest catalytic activity and produces polyethylene with the highest molecular weight.