共轭微孔聚合物
环加成
催化作用
卟啉
聚合物
聚合
微型多孔材料
共轭体系
钴
二氧化碳
材料科学
化学工程
溶剂
化学
有机化学
工程类
作者
Xiaofeng Zhang,Junhong Wang,Yunpeng Bian,Lv Hui-Juan,Bo Qiu,Yuanyuan Zhang,Ruiyuan Qin,Dandan Zhu,Sheng Zhang,Dajian Li,Shimin Wang,Wenpeng Mai,Yue Li,Tao Li
标识
DOI:10.1016/j.jcou.2022.101924
摘要
Conversion of carbon dioxide to cyclic carbonates and other value-added commercial products is a promising strategy for the modern chemical industry and removing CO2 from the atmosphere. Catalysis with high-efficient is critical to the successful conversion of CO2 into cyclic carbonates. Porous organic polymers (POPs) with integrated metalloporphyrin structures are known as typical efficient catalysts for the cycloaddition of CO2 reaction. However, the high cost and energy consumption in synthesizing polymer still prohibit the application of CO2 conversion. Here, we have prepared porphyrin-based conjugated microporous polymer (Co-Por-POPs) microspheres by a simple self-polymerization strategy, which exhibit high catalytic performances in the CO2 cycloaddition reactions with free solvent under atmospheric pressure at room temperature. Even using dilute CO2 (15% CO2 in N2), a TOF up to 8.1 h−1 could be afforded under ambient conditions (25 °C, 1 bar) by Co-Por-POP-2. This study highlights the potential for sustainable industrial syntheses of cyclic carbonates.
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