化学
磷化氢
共聚物
丙烯酸酯
镍
乙烯
催化作用
高分子化学
有机化学
聚合物
作者
John R. Rivet,Briana S. Henderson,Steve Marshall,Keosha Cade,David R. Wilson,Heather A. Spinney,Jianbo Hou,Alex J. Nett
出处
期刊:Organometallics
[American Chemical Society]
日期:2024-04-02
卷期号:43 (8): 859-865
被引量:9
标识
DOI:10.1021/acs.organomet.4c00034
摘要
Phosphine–imidate-supported nickel catalysts were synthesized and tested for ethylene/acrylate copolymerization activity. Phosphine–amide metalation studies with (pyridine)2Ni(CH2Si(CH3)3)2 (py2Ni(CH2TMS)2) suggest that the metalation proceeds via an intermediate phosphine–amide complex ([P,O–amide]Ni(CH2TMS)2). Subsequent deprotonation of the amide N–H gives access to the phosphine–imidate-supported nickel complex ([P,O–imidate]pyNi(CH2TMS)). The imidate form of the ligand proved to be critical for polymerization activity. The phosphine–imidate nickel catalysts described herein were capable of producing ethylene/acrylate copolymers with molecular weights (Mw) from 700 to 120,000 g/mol and with acrylate incorporation >2.6 mol % in some cases. It was determined that hemilabile alkoxy groups on the phosphine aryl groups were necessary to achieve high Mw and acrylate incorporation. These results demonstrate that phosphine–amides, a well-studied ligand class, can be utilized in the imidate form to access highly active neutral nickel polymerization catalysts.
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