聚烯烃
催化作用
化学
离子键合
共聚物
位阻效应
乙烯
聚合
化学工程
均相催化
配体(生物化学)
高分子化学
星团(航天器)
组合化学
多相催化
离子液体
工作(物理)
金属
同种类的
作者
Yu Fl,Mei‐Yan Xu,Binyuan Liu,Changle Chen,Chen Zou
摘要
The performance regulation of polyolefin catalysts typically relies on complex ligand design and synthesis, which limits the rapid development of high-performance polyolefins. The heterogenization of homogeneous catalysts presents a promising and industrially favorable approach to modulate and enhance the performance of transition-metal catalysts. This work introduces a general ionic cluster catalyst assembly (ICCA) strategy to achieve efficient in situ heterogenization without the need for any catalyst supports. It transforms known hydroxyl-functionalized transition-metal catalysts into ionic cluster assemblies by a simple one-step reaction. The steric hindrance of the catalyst metal center can be easily tuned by varying the feed ratios for assembly, without requiring the synthesis of new catalysts. This ICCA strategy enables up to 20 times higher activity during ethylene homo- and copolymerization while significantly improving the molecular weight and mechanical properties of the resulting copolymers. Furthermore, the in situ heterogeneous polymerization facilitated by this strategy demonstrates efficient heat transfer, lower system viscosity, and excellent fouling resistance during polymerization, indicating great potentials for scale-up polymerization. This work provides a general and efficient platform for tuning polyolefin catalyst performance.
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