Synthesis, characterization and ethylene polymerization behavior of nickel dihalide complexes bearing bulky unsymmetrical α-diimine ligands

Hao Liu; Weizhen Zhao; Jiangang Yu; Wenhong Yang; Xiang Hao; Carl Redshaw; Langqiu Chen; Wen-Hua Sun

doi:10.1039/C1CY00319D

Synthesis, characterization and ethylene polymerization behavior of nickel dihalide complexes bearing bulky unsymmetrical α-diimine ligands

Hao Liu, Weizhen Zhao, Jiangang Yu, Wenhong Yang, Xiang Hao, Carl Redshaw, Langqiu Chen, Wen-Hua Sun

Research output: Contribution to journal › Article › peer-review

103 Citations (Scopus)

Abstract

A series of nickel(II) dihalide complexes (C1–C10) bearing unsymmetrical a-diimine ligands of the type 2,4-dibenzhydryl-N-(2-phenyliminoacenaphthylenylidene)-6-methylbenzenamine (L1–L5) were synthesized and fully characterized. Single-crystal X-ray diffraction revealed a distorted tetrahedral geometry around the nickel center in the complexes C3, C5 and C9. Upon activation with modified methylaluminoxane (MMAO), all nickel pro-catalysts performed with high activities in ethylene polymerization, producing highly branched polyethylene products

Original language	English
Pages (from-to)	415-422
Number of pages	8
Journal	Catalysis Science & Technology
Volume	2
Issue number	2
DOIs	https://doi.org/10.1039/C1CY00319D
Publication status	Published - 2012

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10.1039/C1CY00319D

Cite this

@article{57a8f45d40ce420dae7f8e5fd607c306,

title = "Synthesis, characterization and ethylene polymerization behavior of nickel dihalide complexes bearing bulky unsymmetrical α-diimine ligands",

abstract = "A series of nickel(II) dihalide complexes (C1–C10) bearing unsymmetrical a-diimine ligands of the type 2,4-dibenzhydryl-N-(2-phenyliminoacenaphthylenylidene)-6-methylbenzenamine (L1–L5) were synthesized and fully characterized. Single-crystal X-ray diffraction revealed a distorted tetrahedral geometry around the nickel center in the complexes C3, C5 and C9. Upon activation with modified methylaluminoxane (MMAO), all nickel pro-catalysts performed with high activities in ethylene polymerization, producing highly branched polyethylene products",

author = "Hao Liu and Weizhen Zhao and Jiangang Yu and Wenhong Yang and Xiang Hao and Carl Redshaw and Langqiu Chen and Wen-Hua Sun",

year = "2012",

doi = "10.1039/C1CY00319D",

language = "English",

volume = "2",

pages = "415--422",

journal = "Catalysis Science & Technology",

issn = "2044-4753",

publisher = "Royal Society of Chemistry",

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TY - JOUR

T1 - Synthesis, characterization and ethylene polymerization behavior of nickel dihalide complexes bearing bulky unsymmetrical α-diimine ligands

AU - Liu, Hao

AU - Zhao, Weizhen

AU - Yu, Jiangang

AU - Yang, Wenhong

AU - Hao, Xiang

AU - Redshaw, Carl

AU - Chen, Langqiu

AU - Sun, Wen-Hua

PY - 2012

Y1 - 2012

N2 - A series of nickel(II) dihalide complexes (C1–C10) bearing unsymmetrical a-diimine ligands of the type 2,4-dibenzhydryl-N-(2-phenyliminoacenaphthylenylidene)-6-methylbenzenamine (L1–L5) were synthesized and fully characterized. Single-crystal X-ray diffraction revealed a distorted tetrahedral geometry around the nickel center in the complexes C3, C5 and C9. Upon activation with modified methylaluminoxane (MMAO), all nickel pro-catalysts performed with high activities in ethylene polymerization, producing highly branched polyethylene products

AB - A series of nickel(II) dihalide complexes (C1–C10) bearing unsymmetrical a-diimine ligands of the type 2,4-dibenzhydryl-N-(2-phenyliminoacenaphthylenylidene)-6-methylbenzenamine (L1–L5) were synthesized and fully characterized. Single-crystal X-ray diffraction revealed a distorted tetrahedral geometry around the nickel center in the complexes C3, C5 and C9. Upon activation with modified methylaluminoxane (MMAO), all nickel pro-catalysts performed with high activities in ethylene polymerization, producing highly branched polyethylene products

U2 - 10.1039/C1CY00319D

DO - 10.1039/C1CY00319D

M3 - Article

SN - 2044-4753

VL - 2

SP - 415

EP - 422

JO - Catalysis Science & Technology

JF - Catalysis Science & Technology

IS - 2

ER -