MOLECULAR-ORBITAL AND IMOMM STUDIES OF THE CHAIN TRANSFER MECHANISMS OF THE DIIMINE-M(II)-CATALYZED (M = NI, PD) ETHYLENE POLYMERIZATION REACTION

Associative displacement and H-exchange chain transfer/termination mec hanisms for the diimine-M(II)-catalyzed (M = Ni, Pd) ethylene polymeri zation have been studied using B3LYP and IMOMM methods. For unsubstitu ted diimine complexes the coordination of ethylene to the metal-olefin -hydride complexes L2M(C2H4)H+ and L2M(C3H6)H+ is exothermic and gives the five-coordinate complex 22. From 22, the following processes can take place: (a) the associative displacement, path E, corresponding to dissociation of propylene, (b) the dissociation of ethylene, reverse path D, (c) the H-exchange, path F, and (d) the reattaching of the hyd rogen to the polymer chain, path G. For M = Ni, the associative displa cement cannot compete with paths F and G and is unlikely to take place . For M = Pd, the energetics for the paths E-G are similar, and the ch ain transfer/termination via the associative dissociation path E is mo re likely. The H-exchange process, path F, is the most favorable chain transfer/termination mechanism for both metals and includes (a) oxida tive addition of the beta-agostic C beta-H-agostic bond to the metal c enter to form the metalolefin-hydride complex 21, (b) the coordination of ethylene to the metal center to form the five-coordinate complex 2 2, and (c) migration of the hydrogen atom from the metal to the ethyle ne molecule. The rate-determining steps are steps a and c for the diim ine-Ni- and diimine-Pd-catalyzed reactions, respectively. The substitu tion of the imine hydrogens with bulky aromatic groups 2,6-C6H3(i-Pr)( 2) makes 22 thermodynamically unstable relative to C2H4 + diimine-M(C3 H7)(+). Therefore, all processes starting from 22 become unimportant. These results were compared with the previously studied beta-hydrogen transfer and hydrogenolysis chain transfer mechanisms.