Porous Metallosalen Hypercrosslinked Ionic Polymers for Cooperative CO2 Cycloaddition Conversion

被引:38
|
作者
Li, Jing [1 ,2 ]
Han, Yulan [3 ]
Ji, Tuo [1 ]
Wu, Nanhua [2 ,4 ]
Lin, Han [1 ]
Jiang, Jun [3 ]
Zhu, Jiahua [1 ]
机构
[1] Univ Akron, Dept Chem & Biomol Engn, Intelligent Composites Lab, Akron, OH 44325 USA
[2] Nanjing Tech Univ, Coll Chem Engn, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, State Key Lab Mat Oriented Chem Engn, Nanjing 211816, Peoples R China
[3] Univ Sci & Technol China, Sch Chem & Mat Sci, Hefei 230026, Peoples R China
[4] Lulea Univ Technol, Div Energy Sci, Energy Engn, S-97187 Lulea, Sweden
关键词
CARBON-DIOXIDE; CYCLIC CARBONATES; HETEROGENEOUS CATALYSTS; CHEMICAL FIXATION; ORGANIC POLYMERS; EFFICIENT; EPOXIDES; CAPTURE; COMPLEX; SITES;
D O I
10.1021/acs.iecr.9b05304
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Metallosalen-based porous ionic polymers have the potential to combine the merits of homogeneous organometallics and heterogeneous porous ionic catalysts in carbon dioxide (CO2) cycloaddition conversion. Herein, a series of porous metallosalen hypercrosslinked ionic polymers (M-HIPs) were synthesized through a simple method. The M-HIPs with high metal and Br anion concentrations were evaluated by catalyzing CO2 cycloaddition with epoxides. Because of the cooperative effect between Br anions and metal active species in the porous channel, M-HIPs exhibited a high CO2 catalytic performance even under ambient conditions. Among the M-HIPs (M = Co, Al, Zn), Co-HIP showed the best catalytic performance for various epoxides and was stable after five runs. Density functional theory calculations support the fact that Co-HIP had the lowest energy barrier, which agreed with the experimental results.
引用
收藏
页码:676 / 684
页数:9
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