Cationic P,O‐Coordinated Nickel(II) Catalysts for Carbonylative Polymerization of Ethylene: Unexpected Productivity via Subtle Electronic Variation
Shi‐Yu Chen, Bai‐Hao Ren, Shi‐Huan Li, Yuhang Song, Shuang Jiao, Chen Zou, Changle Chen, Xiao‐Bing Lu, Ye Liu
Abstract
Abstract Transition‐metal‐catalyzed copolymerization of ethylene with carbon monoxide affords polyketones materials with excellent mechanical strength, photodegradability, surface and barrier properties. Unlike the widely used and rather expensive Pd catalysts, Ni‐catalyzed carbonylative polymerization is very difficult since the strong binding affinity of CO to Ni deactivates the highly electrophilic metal center easily. In this study, various cationic P,O‐coordinated Ni complexes were synthesized using the electronic modulation strategy, and the catalyst with strong electron‐donating substituents exhibits an excellent productivity of 10 4 g polymer (g Ni) −1 , which represents a rare discovery that a Ni complex could operate with such exceptional efficiency in comparison with Pd catalysts. Notably, those Ni catalysts were also efficient for terpolymerization of ethylene, propylene with CO for producing commercial polyketone materials with low melting temperatures and easy processibility.