Scalable, Durable, and Recyclable Metal-Free Catalysts for Highly Efficient Conversion of CO2to Cyclic Carbonates

被引:139
作者
Zhang, Yao-Yao [1 ]
Yang, Guan-Wen [1 ]
Xie, Rui [1 ]
Yang, Li [1 ]
Li, Bo [2 ]
Wu, Guang-Peng [1 ]
机构
[1] Zhejiang Univ, MOE Lab Macromol Synth & Functionalizat Adsorpt &, Dept Polymer Sci & Engn, Zhe Da Rd 38, Hangzhou 310027, Peoples R China
[2] Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, Yuhangtang Rd 2318, Hangzhou 311121, Peoples R China
基金
中国国家自然科学基金;
关键词
cycloaddition; CO(2)capture; cooperative mechanisms; cyclic carbonates; metal-free catalysts; IONIC LIQUIDS; CO2; FIXATION; ORGANIC CARBONATES; BIFUNCTIONAL CATALYSTS; MEDIATED FORMATION; ALUMINUM CATALYST; DIOXIDE FIXATION; EPOXIDES; ORGANOCATALYSTS; CYCLOADDITION;
D O I
10.1002/anie.202010651
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 degrees 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.
引用
收藏
页码:23291 / 23298
页数:8
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