Ethylene Dimerization/Polymerization Catalyzed by (Adamantylimido)vanadium(V) Complexes Containing (2-Anilidomethyl)pyridine Ligands: Factors Affecting the Ethylene Reactivity

Abstract

V­(N-1-adamantyl)­Cl<sub>2</sub>[2-(2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)­NCH<sub>2</sub>(C<sub>5</sub>H<sub>4</sub>N)] showed both remarkable activity and selectivity (from 92 through >99.5% selectivity) in ethylene dimerization in the presence of MAO or MMAO, and the activity increased linearly upon increasing the ethylene pressure. The same reaction in the presence of Et<sub>2</sub>AlCl or Me<sub>2</sub>AlCl afforded ultrahigh molecular weight polyethylene. Both the ESR spectra and the <sup>51</sup>V NMR spectra suggest that the chelate anionic donor ligand plays an important role in stabilization of the oxidation state in the catalyst solution even containing Al alkyls

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