4.5 Article

New octahedral bis-α-diimine nickel(II) complexes containing chloro-substituted aryl groups: Synthesis, characterization and testing as ethylene polymerisation catalysts

Journal

JOURNAL OF ORGANOMETALLIC CHEMISTRY
Volume 696, Issue 20, Pages 3251-3256

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2011.07.009

Keywords

alpha-Diimine; Branched polyethylene; Crystal structure; Ethylene; Nickel complex; Polymerization

Funding

  1. National Natural Science Foundation of China [20964003]
  2. Key Laboratory of Eco-Environment-Related Polymer Materials of Ministry of Education
  3. Key Laboratory of Polymer Materials of Gansu Province (Northwest Normal University)
  4. Fundacao para Ciencia e Tecnologia [PTDC/EQU-EQU/110313/2009]
  5. FEDER

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Three new 20-electron bis-alpha-diimine nickel (II) complexes containing chloro-substituted ligands, bis{bis [N,N'-(3-chloro-2-methylphenyl)imino]-1,2-dimethylethane}dibromonickel 2a, bis{bis[N,N'-(3-chloro-2,6-dimethylphenyl) imino]-1,2-dimethylethane}dibromonickel 2b and bis{bis[N,N'-(4-chloro-2,6-dimethylphenyl) imino]-1,2-dimethylethane} dibromonickel 2c, were synthesized and characterized. The molecular structure of complex 2a was determined by X-ray crystallography. In the solid state, complex 2a has a pseudooctahedral geometry about the nickel center, containing two a-diimine ligands in the pseudo-equatorial plane and two trans bromide ligands occupying the axial positions. These complexes, activated by diethylaluminum chloride (DEAC) were tested in the polymerization of ethylene under mild conditions. NMR analysis shows that highly branched polyethylenes are obtained using these bis-a-diimine nickel(II) complexes containing electron-withdrawing Cl groups in the aryl groups (e. g. 84 branches/1000 C, at 20 degrees C). The catalytic activity, polymer molecularweight and polymer degree of branching were significantly affected by the number of methyl substituents in the ortho-aryl position and the chlorine substituent position in the aryl rings of the coordinated a-diimine ligands. (C) 2011 Elsevier B.V. All rights reserved.

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