

FOLLOWUS
a.Hebei Key Laboratory of Functional Polymers, Tianjin Key Laboratory of Chemical Process Safety, Institute of Polymer Science and Engineering, Hebei University of Technology, Tianjin 300130, China
b.State Key Laboratory of Separation Membranes and Membrane Processes, School of Material Science and Engineering, Tiangong University, Tianjin 300160, China
c.Lanzhou Petrochemical Research Center, Petrochemical Research Institute of CNPC, Lanzhou 730060, China
houyh1977@163.com (Y.H.H.)
polyym@163.com (M.Y.)
Received:10 February 2020,
Revised:2020-3-18,
Accepted:20 March 2020,
Online First:01 June 2020,
Published:14 August 2020
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Zhang, R. F.; Hou, Y. H.; Wei, X. L.; Zhao, D. D.; Cui, M. M.; Zhai, F. F.; Li, X. L.; Liu, B. Y.; Yang, M. Thermostable , α,-diimine nickel complexes with substituents on acenaphthequinone-backbone for ethylene polymerization. Chinese J. Polym. Sci. 2020, 38, 1214–1220
Rui-Fang Zhang, Yan-Hui Hou, Xu-Ling Wei, et al. Thermostable
Zhang, R. F.; Hou, Y. H.; Wei, X. L.; Zhao, D. D.; Cui, M. M.; Zhai, F. F.; Li, X. L.; Liu, B. Y.; Yang, M. Thermostable , α,-diimine nickel complexes with substituents on acenaphthequinone-backbone for ethylene polymerization. Chinese J. Polym. Sci. 2020, 38, 1214–1220 DOI: 10.1007/s10118-020-2430-x.
Rui-Fang Zhang, Yan-Hui Hou, Xu-Ling Wei, et al. Thermostable
In order to promote the thermostability of
α
-diimine nickel complex by ligand backbone structure
a series of
α
-diimine nickel complexes with substituents on acenaphthequinone backbone were synthesized and used as catalysts for ethylene polymerization. When the hydroxyethyl phenoxyl group was introduced to the acenaphthequinone-backbone
the thermal stability and activity of the catalyst could be significantly improved. The catalytic activity of complex
C2
[5-(4-(2-hydroxyethyl)phenoxyl)-
N
N
-bis(2
6-diisopropyl)acenaphthylene-1
2-diimine]nickel(II) dibromide with isopropyl substituents on
N
-aryl reached 8.2 × 10
6
g/(mol
Ni
·h) at 70 °C and 2 MPa. The activity of [5-(4-(2-hydroxyethyl)phenoxyl)-
N
N
-bis(2
6-dibenzhydryl-4-menthylphenyl)acenaphthylene-1
2-diimine]nickel(II) dibromide (
C3
) still maintained at 6.7 × 10
5
g/(mol
Ni
·h) at 120 °C. Compared with
C3
containing bulky dibenzhydryl substituents
the activity of
C2
was sensitive to the change of the polymerization pressure. However
the polyethylenes obtained from complex
C3
had lower branching density. Meanwhile
the molecular weight could reach 971 kg/mol
which is almost 5 times as much as that of the polyethylene obtained from complex
C2
.
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