Affiliation:
1. MOE Key Laboratory of Macromolecular Synthesis and Functionalization Department of Polymer Science and Engineering Zhejiang University Yuhangtang Road 866 Hangzhou 310058 P. R. China
2. ZJU‐Hangzhou Xinglu High‐end Polyolefin Research & Development Center Hangzhou 310058 P. R. China
3. Shanxi‐Zheda Institute of Advanced Materials and Chemical Engineering Hangzhou 310058 P. R. China
4. Hangzhou Xinglu Technologies Co. Ltd. Hangzhou 310012 P. R. China
Abstract
AbstractThe thermal stability of α‐diimine nickel catalysts has always been the focus of research. The introduction of large groups in the backbone or N‐aryl ortho‐position is a relatively mature solution. However, the question of whether the N‐aryl bond rotation is a factor affecting the thermal stability of nickel catalysts is still open. In this work, the effects of N‐aryl para‐benzhydryl substitutes on catalyst thermal stability are investigated, and the results of ethylene polymerization and the factors affecting thermal stability (steric effect, electronic effect, five‐membered coordination ring stability, N‐aryl bond rotation, etc.) are systematically analyzed. It is believed that the introduction of large steric hindrance groups at the N‐aryl para‐position hinders the rotation of the N‐aryl bond. This obstacle effect is beneficial to improving catalyst thermal stability, and the obstacle capacity is weakened with the increase of ortho‐substituent size.
Subject
Materials Chemistry,Polymers and Plastics,Organic Chemistry
Cited by
1 articles.
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