Nickel(II) and Palladium(II) Polymerization Catalysts Bearing a Fluorinated Cyclophane Ligand: Stabilization of the Reactive Intermediate

The synthesis and characterization of Ni(II) and Pd(II) α-diimine olefin polymerization catalysts bearing a fluorinated cyclophane-based ligand were performed. Fluorine was placed in such a manner as to interact with the metal center from the axial direction. The catalysts were active in the polymerization of ethylene, showing substantial differences in both catalytic behavior and polymer size and structure as compared to their nonfluorinated analogues. Both catalysts afforded polymer of comparatively low branching density and high molecular weight. The Ni(II) catalysts, from precursor Ni(acetylacetonato)(F-Cyc) + salts (F-Cyc = fluorinated cyclophane), exhibited enhanced thermal stability by remaining active after 70 min with little loss in polymerization activity at 105 °C. The Pd(II) catalysts from salts of Pd(F-Cyc)Me(NCR) + (NCR = nitrile) afforded polymer of molecular weights far higher than the nonfluorinated analogue. Additionally, polymerization activity was directly related to ethylene feed pressure for the Pd(II) system, and NMR analysis could not detect the presence of bound olefin, indicating that the polymerization proceeded via different kinetics involving an olefin-free 14 e − complex as the catalyst resting state. Furthermore, NMR 1 H− 19 F coupling data provide clear evidence that the fluorine atoms were indeed interacting with the metal axial site. The unusual properties of these new complexes are thus attributed to stabilization of the highly reactive 14 e − intermediate by donation of the fluorine lone pair to the metal center.