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Updated: Sep 8, 2025

Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
Published on: November 27, 2015
ortho/para-Chlorinated α‑Diimine Nickel Precatalysts Resulting Polyethylenes with Improved Mechanical Properties and
Aoqian Xi1,2, Qiuyue Zhang2, Yanning Zeng1
1College of Materials Science and Engineering, Guilin University of Technology, Qixing District, Guilin 541004, China.
Abstract:
A series of ortho/para-chlorinated N-(6-benzhydryl-2,4-dichlorophenylimino)-N'-aryliminoacenaphthylene derivatives as ligands (L1-L6, aryl = 2,6-dimethylphenyl (L1), 2,6-diethylphenyl (L2), 2,6-diisopropylphenyl (L3), 2,4,6-trimethylphenyl (L4), 2,6-diethyl-4-methylphenyl (L5), 6-benzhydryl-2,4-dichlorophenyl (L6)) were successfully synthesized and used for their corresponding nickel complexes (Ni1-Ni6). All organic compounds were comprehensively characterized using NMR, FT-IR, and EA techniques; the nickel complexes had their components determined through FT-IR and EA analysis, and the unambiguous molecular structures of representative nickel complexes were confirmed via single-crystal X-ray diffraction, revealing that Ni1 and Ni3 possessed a distorted octahedral geometry around the nickel center. Upon activation with EASC, all nickel complexes demonstrated high catalytic activity (4.7 to 37.9 × 106 g mol-1 h-1) for ethylene polymerization, with Ni1 achieving peak performance (12.2 × 106 g mol-1 h-1) at 50 °C in 30 min. Impressively, the catalytic system demonstrated exceptional thermal stability, maintaining high activity above 9 × 106 g mol-1 h-1 across a broad temperature range (40-70 °C) with minimal fluctuations. Contrary to typical chain-walking behavior observed in α-diimine nickel catalysts, the resultant polyethylene exhibited high crystallinity and minimal long-chain branching despite narrow polydispersity (Đ = 1.8-2.9) and moderate molecular weights (tens of thousands). Systematic modulation of ligand structure and polymerization conditions enabled precise control over crystallinity (X c: 6.4 to 62.6%), which was directly correlated with tunable mechanical properties (σb: 1.9-13.1 MPa, εb: 178.8-1030.6%). Representative samples of the resultant polyethylene displayed exceptional tensile strength (13.1 MPa), high elongation at break (1030.6%), and notable elastic recovery (65%), suggesting new types of thermoplastic elastomers.
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