4.7 Article

Direct Synthesis of Chain-End Toluene Functionalized Hyperbranched Ethylene Oligomers

Journal

POLYMERS
Volume 14, Issue 15, Pages -

Publisher

MDPI
DOI: 10.3390/polym14153049

Keywords

iminopyridine Ni(II) complexes; ethylene oligomerization; hyperbranched; toluene-end-functionalized

Funding

  1. Natural Science Foundation of Anhui Province [2108085Y06]
  2. Anhui Provincial Key Laboratory Open Project Foundation [LCECSC-01]

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In this study, chain-end functionalized polymers were successfully synthesized and ethylene oligomers were provided through catalytic reactions. It was found that toluene-end-functionalized hyperbranched ethylene oligomers could be obtained under elevated temperature conditions, which was caused by the tandem catalysis of ethylene oligomerization and the subsequent Friedel-Crafts addition of the resulting unsaturated products to toluene molecules.
Chain-end functionalized polymers play an important role in the field of building complex macromolecular structures. In this study, we have synthesized and characterized four dibenzhydryl iminopyridine Ni(II) complexes bearing remote flexible substituents (Et and n-Bu) to provide hyperbranched ethylene oligomers in ethylene oligomerization with moderate to good activities. Most notably, toluene-end-functionalized hyperbranched ethylene oligomers were obtained under elevated temperature conditions and validated by NMR. The tandem catalysis of ethylene oligomerization and the subsequent Friedel-Crafts addition of the resulting unsaturated products to toluene molecules was proposed as the cause of the observed phenomenon.

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