a.College of Chemistry and Life Science, Advanced Institute of Materials Science, Changchun University of Technology, Changchun 130012, China
b.Key Laboratory of Advanced Structural Materials of Ministry of Education, College of Material Science and Engineering, Changchun University of Technology, Changchun 130012, China
c.State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China
yuechi@ccut.edu.cn (Y.C.)
zhangyixin@ciac.ac.cn (Y.X.Z.)
zbjian@ciac.ac.cn (Z.B.J.)
收稿:2021-01-14,
修回:2021-2-5,
录用:2021-2-9,
网络首发:2021-04-30,
纸质出版:2021-06-18
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Wang, Y. Y.; Wang, C. Q.; Hu, X. Q.; Xia, Y.; Chi, Y.; Zhang, Y. X.; Jian, Z. B. Benzosuberyl substituents as a "sandwich-like" function in olefin polymerization catalysis. Chinese J. Polym. Sci. 2021, 39, 984–993
Yu-Yin Wang, Chao-Qun Wang, Xiao-Qiang Hu, et al. Benzosuberyl Substituents as a "Sandwich-like" Function in Olefin Polymerization Catalysis[J]. Chinese Journal of Polymer Science, 2021, 39(8): 984-993.
Wang, Y. Y.; Wang, C. Q.; Hu, X. Q.; Xia, Y.; Chi, Y.; Zhang, Y. X.; Jian, Z. B. Benzosuberyl substituents as a "sandwich-like" function in olefin polymerization catalysis. Chinese J. Polym. Sci. 2021, 39, 984–993 DOI: 10.1007/s10118-021-2562-7.
Yu-Yin Wang, Chao-Qun Wang, Xiao-Qiang Hu, et al. Benzosuberyl Substituents as a "Sandwich-like" Function in Olefin Polymerization Catalysis[J]. Chinese Journal of Polymer Science, 2021, 39(8): 984-993. DOI: 10.1007/s10118-021-2562-7.
For the rational design of metal catalyst in olefin polymerization catalysis
various strategies were applied to suppress the chain transfer by bulking up the axial positions of the metal center
among which the ”sandwich” type turned out to be an efficient category in achieving high molecular weight polyolefin. In the
α
-diimine system
the “sandwich” type catalysts were built using the typical 8-aryl-naphthyl framework. In this contribution
by introducing the rotationally restrained benzosuberyl substituent into the
ortho
-position of
N
-aryl rings
a new class of “sandwich-like”
α
-diimine nickel catalysts was constructed and fully identified. The rotationally restrained benzosuberyl substituents played a “sandwich-like” function by capping the nickel center from two axial sites. Compared to the nickel catalyst
Ni1
bearing freely rotated benzhydryl substituent
Ni2
featuring benzosuberyl substituent enabled the increase (8 times) of polymer molecular weights from 8 kDa to 65 kDa in the polymerization of ethylene. By further increasing the steric bulk of another
ortho
-site of the
N
-aryl ring
the polymer molecular weight even reached an ultrahigh level of 833 kDa (
M
w
=1857 kDa) using the optimized
Ni3
. Notably
these nickel catalysts could also mediate the copolymerization of ethylene with methyl 10-undecenoate
with
Ni3
giving the highest copolymer molecular weight (88 kDa) and the highest incorporation of comonmer (2.0 mol%)
along with high activity of up to 10
5
g·mol
−1
·h
−1
.
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