催化作用
热稳定性
金属
环氧化物
分子内力
偶联反应
材料科学
反应性(心理学)
化学工程
组合化学
化学
有机化学
酶
替代医学
病理
工程类
医学
作者
Yao‐Yao Zhang,Guan‐Wen Yang,Rui Xie,Li Yang,Bo Li,Guang‐Peng Wu
标识
DOI:10.1002/anie.202010651
摘要
Abstract A series of highly active organoboron catalysts for the coupling of CO 2 and epoxides with the advantages of scalable preparation, thermostability, and recyclability is reported. The metal‐free catalysts show high reactivity towards a wide scope of cyclic carbonates (14 examples) and can withstand a high temperature up to 150 °C. Compared with the current metal‐free catalytic systems that use mol % catalyst loading, the catalytic capacity of the catalyst described herein can be enhanced by three orders of magnitude (epoxide/cat.=200 000/1, mole ratio) in the presence of a cocatalyst. This feature greatly narrows the gap between metal‐free catalysts and state‐of‐the‐art metallic systems. An intramolecular cooperative mechanism is proposed and certified on the basis of investigations on crystal structures, structure–performance relationships, kinetic studies, and key reaction intermediates.
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