This paper reports the polymerization of 1-octadecene catalyzed by a series of ?-diimine Ni(II) complex, with methyl ligand backbone and different substituents in the ortho and para aryl positions, in combination with Et2AlCl. We obtained semicrystalline ethylene-propylene-1-octadecene terpolymers with high molecular weight and narrow molecular weight distribution. The formation of such terpolymers is due to the numerous combi- nations of insertion and chain-walking pathways. The effect of the type of ligand and monomer feedstock concentration on the activity, regioselectivity, polymers (micro)structure, and structure/properties is thoroughly investigated by NMR, DSC, WAXD and SAXS. The thermal behavior and the crystal structure of the polymers are strongly influenced by the level of incorporation of methyl and longer alkyl branches. The chain heterogeneity of the polymers is investigated by successive self-nucleation and annealing thermal fractionation evaluating the crystallizable sequence length, and the lamellar thickness.
(Micro)structure, thermal behavior and mechanical properties of ethylene-propylene-1-octadecene terpolymers from chain-walking polymerization of 1-octadecene
Giuseppe Leone;Maurizio Canetti;Ivana Pierro;Giorgia Zanchin;Giovanni Ricci;Fabio Bertini
2019
Abstract
This paper reports the polymerization of 1-octadecene catalyzed by a series of ?-diimine Ni(II) complex, with methyl ligand backbone and different substituents in the ortho and para aryl positions, in combination with Et2AlCl. We obtained semicrystalline ethylene-propylene-1-octadecene terpolymers with high molecular weight and narrow molecular weight distribution. The formation of such terpolymers is due to the numerous combi- nations of insertion and chain-walking pathways. The effect of the type of ligand and monomer feedstock concentration on the activity, regioselectivity, polymers (micro)structure, and structure/properties is thoroughly investigated by NMR, DSC, WAXD and SAXS. The thermal behavior and the crystal structure of the polymers are strongly influenced by the level of incorporation of methyl and longer alkyl branches. The chain heterogeneity of the polymers is investigated by successive self-nucleation and annealing thermal fractionation evaluating the crystallizable sequence length, and the lamellar thickness.File | Dimensione | Formato | |
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