Me), have been synthesized and fully characterized by multi-nuclear NMR spectroscopy, elemental analysis, and single crystal X-ray diffraction studies. These complexes were immobilized on an insoluble polymethylaluminoxane (sMAO), MAO-modified silica (ssMAO) and a MAO-modified layered double hydroxide (LDH-MAO). The effect of substitution around the Cp ligand was examined in relation to their performance (activity, M w , PDI, morphology) for ethylene polymerization measured both in solution and in slurry phase. Maximum solution-phase activities of 3585 kg/mol.h.bar were recorded at modest [Zr]:[Al] ratios of 1:250. These were compared to the activities recorded using the equivalent solid supported complexes, we observed that sMAO was a superior support material with average increases in activity of 5.3 and 2.3 times relative to ssMAO and LDH-MAO respectively. Most striking was the observation that slurry-phase ethylene polymerization activities using equivalent pro-catalysts supported on sMAO showed enhanced performance compared to the solution phase up to a maximum of 4486 kg/mol.h.bar.