Abstract

A series of late-transition metal complexes supported with chlorinated bis(arylimino)pyridine ligands [2,6-(ArNCCl)2C5H3N]MtCl2 (Ar = 2,4,6-Me3C6H2, Mt = Fe (1a), Co (2a), Ni (3a); Ar = 2,6-iPr2C6H3, Mt = Fe (1b), Co (2b); Ar = 2,6-Et2C6H3, Mt = Co (1c), Ni (3c); Ar = 2,6-Me2C6H3, Mt = Fe (1d), Co (2d); Ar = 4-Cl-2,6-Me2C6H2, Mt = Fe (1e), Co (2e); Ar = 4-Br-2,6-Me2C6H2, Mt = Fe (1f), Co (2f)) were synthesized. At the presence of methylaluminoxane (MAO), Fe(II)- and Co(II)- based complexes were highly active towards ethylene polymerization, affording polymers with bimodal and unimodal molar mass distributions, respectively, while the Ni(II)-based complexes gave no polymer products. Moreover, the obtained polyethylenes were predominately saturated and vinyl-terminated for Fe(II)- and Co(II)-based complexes, respectively. Changing the ligand environment, polymerization parameters also posed a great influence on the catalytic activities and the properties of the resulting polymers.

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