Tunable “in-chain” and “at the end of the branches” methyl acrylate incorporation in the polyolefin skeleton through Pd (II) catalysis

The synthesis of functionalized polyolefins through coordination-insertion polymerization is a highly challenging reaction. The ideal catalyst, in addition to showing a high productivity, has to be able to control the copolymer microstructure and, in particular, the way of the polar vinyl monomer incorporation. In this contribution, we modified the typical Brookhart's catalyst by introducing in the fourth coordination site of palladium a hemilabile, potentially bidentate ligand, such as a thiophenimine (N-S). The obtained cationic Pd(II) complexes, [Pd(Me)(N-N)(N-S)][PF6], generated active catalysts for the ethylene/methyl acrylate (MA) copolymerization leading to the desired copolymer with a different incorporation of the polar monomer depending on both the reaction medium and the N-S ligand. Surprisingly enough, the produced copolymers have the inserted acrylate both at the end of the branches (T(MA)) and in the main chain (M(MA)) in a ratio M(MA)/T(MA) that goes from 9:91 to 45:55 m...