Direct Synthesis of Polyethylene Thermoplastic Elastomers Using Hybrid Bulky Acenaphthene-Based α-Diimine Ni(II) Catalysts

Abstract

Recently, polyolefin thermoplastic elastomers can be obtained directly using ethylene as a single feedstock via α-diimine nickel-catalyzed ethylene chain walking polymerization. Here, a new range of bulky acenaphthene-based α-diimine nickel complexes with hybrid o-phenyl and -diarylmethyl anilines were constructed and applied to ethylene polymerization. All the nickel complexes under the activation of excess Et2AlCl exhibited good activity (level of 106 g mol−1 h−1) and produced polyethylene with high molecular weight (75.6–352.4 kg/mol) as well as proper branching densities (55–77/1000C). All the branched polyethylenes obtained exhibited high strain (704–1097%) and moderate to high stress (7–25 MPa) at break values. Most interestingly, the polyethylene produced by the methoxy-substituted nickel complex exhibited significantly lower molecular weights and branching densities, as well as significantly poorer strain recovery values (48% vs. 78–80%) than those by the other two complexes under the same conditions.

Keywords

• α-diimine nickel complexes
• branched polyethylenes
• ethylene polymerization
• polyethylene thermoplastic elastomers