ABSTRACT
A series of stable dialkyl complexes of Pd, (alpha-diimine)PdR2 (alpha-diimine = aryl-substituted diimine, R = n-Pr, n-Bu, i-Bu), have been prepared via Grignard alkylation of the corresponding (alpha-diimine)PdCl2 complexes. Protonation of these dialkyl species at low temperature results in loss of alkane and formation of cationic Pd beta-agostic alkyl complexes, which have been observed as intermediates in the polymerization of ethylene and propylene by these Pd catalysts. Studies of the structure and dynamic behavior of these alkyl complexes are presented, along with the results of trapping reactions of these species with ligands such as NCMe, CO, and C2H4. Trapping with ethylene results in formation of cationic alkyl ethylene complexes which model the catalyst resting state in these systems. These complexes have been used to obtain mechanistic details and kinetic parameters of several processes, including isomerization of the alkyl ethylene complexes, associative and dissociative exchange with free ethylene, and migratory insertion rates of both primary and secondary alkyl ethylene species. These studies indicate that the overall branching observed in polyethylenes produced by these Pd catalysts is governed both by the kinetics of migratory insertion and by the equilibria involving the alkyl ethylene complexes.
