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配体主链取代基对用于乙烯聚合及与极性单体共聚的膦羰基钯和镍催化剂的影响

Influences of Ligand Backbone Substituents on Phosphinecarbonylpalladium and -nickel Catalysts for Ethylene Polymerization and Copolymerization with Polar Monomers.

作者信息

Zhu Ningning, Liang Tao, Huang Yongshuang, Pang Wenmin, Chen Min, Tan Chen

机构信息

Hefei National Laboratory for Physical Sciences at the Microscale, CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei 230026, China.

Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education, Institutes of Physical Science and Information Technology, Anhui University, Hefei, Anhui 230601, China.

出版信息

Inorg Chem. 2021 Sep 6;60(17):13080-13090. doi: 10.1021/acs.inorgchem.1c01490. Epub 2021 Aug 6.

Abstract

A series of phosphinecarbonylpalladium and -nickel catalysts bearing various substituents on the ligand backbone were prepared, characterized, and used in ethylene polymerization and copolymerization with polar monomers. The Pd and Ni catalysts can achieve high activities as well as high polymer molecular weights in both ethylene polymerization and copolymerization with polar monomers. The electron-donating group from the carbonyl side can effectively increase the polymer molecular weights. Utilization of a cyclic backbone structure can increase the catalytic activities at the expense of the polymer molecular weights. Moreover, installation of a pyridyl moiety in the ligand backbone can enable Lewis acid responsiveness and can enhance the polymerization activities. These results suggest the importance of the ligand backbone for the properties of catalysts in ethylene polymerization and copolymerization reactions.

摘要

制备了一系列在配体主链上带有各种取代基的膦羰基钯和镍催化剂,对其进行了表征,并将其用于乙烯聚合以及与极性单体的共聚反应。钯和镍催化剂在乙烯聚合以及与极性单体的共聚反应中均能实现高活性以及高聚合物分子量。来自羰基侧的给电子基团可有效提高聚合物分子量。利用环状主链结构可以提高催化活性,但会牺牲聚合物分子量。此外,在配体主链中引入吡啶基部分可实现对路易斯酸的响应,并能提高聚合活性。这些结果表明配体主链对于乙烯聚合和共聚反应中催化剂性能的重要性。

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