

FOLLOWUS
a.School of Chemistry and Chemical Engineering/State Key Laboratory Incubation Base for Green Processing of Chemical Engineering, Shihezi University, Shihezi 832003, China
b.State Key Laboratory of Precision and Intelligent Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei 230026, China
c.Hebei Key Laboratory of Functional Polymer, School of Chemical Engineering and Technology, Hebei University of Technology, Tianjin 300401, China
byliu@hebut.edu.cn (B.Y.L.)
chen1215@ustc.edu.cn (C.Z.)
Received:11 October 2025,
Accepted:13 November 2025,
Published Online:16 January 2026,
Published:05 February 2026
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Yu, F.; Dai, B.; Liu, N.; Liu, B. Y.; Zou, C. Alkyl alcohol chain-length mediated steric hindrance at support surface in heterogeneous α-diimine Ni catalysts for modulating ethylene polymerization. Chinese J. Polym. Sci. 2026, 44, 331–340
Fan Yu, Bin Dai, Ning Liu, et al. Alkyl Alcohol Chain-length Mediated Steric Hindrance at Support Surface in Heterogeneous
Yu, F.; Dai, B.; Liu, N.; Liu, B. Y.; Zou, C. Alkyl alcohol chain-length mediated steric hindrance at support surface in heterogeneous α-diimine Ni catalysts for modulating ethylene polymerization. Chinese J. Polym. Sci. 2026, 44, 331–340 DOI: 10.1007/s10118-025-3501-9.
Fan Yu, Bin Dai, Ning Liu, et al. Alkyl Alcohol Chain-length Mediated Steric Hindrance at Support Surface in Heterogeneous
This work investigates supported
α
-diimine nickel catalysts for ethylene polymerization. By tuning the length of alkyl alcohol chains attached to the ligand
the distance between the nickel center and the MgCl
2
support surface is controlled. This modulation effectively regulates support-induced steric hindrance
influencing catalyst behavior.
Heterogeneous polymerization represents a widely employed method in the polyolefin industry. In recent years
various heterogenization strategies for late transition metal catalysts have been developed
enabling effective control of polymer morphology and optimization of catalytic performance.
However
while most studies have focused on designing anchoring groups and advancing support approaches
systematic investigations into how the support influences the catalytic behavior of the late transition metal catalysts. In this work
we fabricated supported
α
-diimine nickel catalysts by functionalizing the ligand with alkyl alcohol chains of varying lengths and supporting them onto MgCl
2
supports. The ethylene polymerization behavior of these catalysts was then investigated. By precisely adjusting the alkyl alcohol chain length
the distance between the catalytically active metal center and the support surface was modulated. This approach demonstrates that support-induced steric hindrance effect can be effectively regulated by controlling the separation distance between the metal center and the support surface.
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