Introducing electron-donating substituents on ligand backbone of α-diimine nickel complex and the effects on catalyst thermal stability in ethylene polymerization

Abstract

A novel α-diimine nickel pre-catalyst Cat.1 with two electron-donating methyl substituents on the ligand backbone was synthesized and investigated for ethylene polymerization using methylaluminoxane as cocatalyst. Cat.1 exhibited higher polymerization activity and produced highly branched polyethylene with slightly higher molecular weight than that of the typical Brookhart catalyst (B-Cat) at elevated temperature. By tracing the changes of active center number in the polymerization process, Cat.1 was found to have higher ratio of activated nickel ([C∗]/[Ni]), longer catalyst lifetime and larger chain propagation rate constant (kp) as compared with B-Cat. The computational studies demonstrated the electron-donating methyl substituents can make a more electron-rich ligand to influence the catalytic properties of Cat.1. Stronger interactions between the electron-rich ligand and the nickel center should be the main reasons for longer catalyst lifetime and enhanced thermal stability of Cat.1. The production of polyethylene with higher molecular weight by Cat.1 can be explained by its larger kp value and more stable transition state for ethylene insertion than for chain transfer reaction due to the electron-donating ligand. Overall, the results of this work clearly support the importance of ligand electronic effects on the thermal stability and intrinsic reactivity of active centers in α-diimine Ni(II) catalysts.