催化作用
聚合物
聚合
联吡啶
化学工程
材料科学
金属化
多相催化
多孔性
原材料
环加成
化学
有机化学
晶体结构
工程类
作者
Zhifeng Dai,Qi Sun,Xiaolong Liu,Liping Guo,Jixue Li,Shuxiang Pan,Chaoqun Bian,Liang Wang,Xin Hu,Xiangju Meng,Leihong Zhao,Feng Deng,Feng-Shou Xiao,Zhifeng Dai,Qi Sun,Xiaolong Liu,Liping Guo,Jixue Li,Shuxiang Pan,Chaoqun Bian
出处
期刊:Chemsuschem
[Wiley]
日期:2016-11-16
卷期号:10 (6): 1186-1192
被引量:103
标识
DOI:10.1002/cssc.201601375
摘要
Abstract As a C 1 feedstock, CO 2 has the potential to be uniquely highly economical in both a chemical and a financial sense. Porous materials bearing particular binding and active sites that can capture and convert CO 2 simultaneously are promising candidates for CO 2 utilization. In this work, a bipyridine‐constructed polymer featuring a high surface area, a hierarchical porous structure, and excellent stability was synthesized through free‐radical polymerization. After metalation, the resultant catalysts exhibited superior activities in comparison with those of their homogeneous counterparts in the cycloaddition of CO 2 to epoxides. The high performance of the heterogeneous catalysts originates from cooperative effects between the CO 2 ‐philic polymer and the embedded metal species. In addition, the catalysts showed excellent stabilities and are readily recyclable; thus, they are promising for practical utilization for the conversion of CO 2 into value‐added chemicals.
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