Tang Duihai, Wang Tao, Zhang Wenting, Zhao Zhen, Zhang Ling, Qiao Zhen-An
Institute of Catalysis for Energy and Environment, College of Chemistry and Chemical Engineering, Shenyang Normal University, Shenyang, Liaoning 110034, China.
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun, Jilin 130012, China.
Angew Chem Int Ed Engl. 2022 Jul 4;61(27):e202203967. doi: 10.1002/anie.202203967. Epub 2022 May 9.
The functional groups in porous carbon generally suffer a severe loss during the high-temperature carbonization. Instead, the low-temperature synthesis of carbon featuring porous structures and abundant functional groups is not only a solution that evades the pitfalls of pyrolysis but also is of significance for the development of synthetic methodology. Herein, a liquid metal interfacial engineering strategy is reported for the synthesis of porous carbon using CCl as the carbon precursor and sodium-potassium alloy (NaK) as the reducing agent, which is superior to traditional synthetic methods because it enables the engineering of a highly active liquid metal alloy microemulsion to directly generate porous carbon at ambient temperature. As synthesized porous carbon featured abundant carbon-chlorine bonds can be tandem-grafted with imidazole and 1,2-dibromoethane to achieve a CO cycloaddition catalyst, which exhibits excellent catalytic activity, in addition to exceptional stability.
多孔碳中的官能团在高温碳化过程中通常会严重损失。相反,低温合成具有多孔结构和丰富官能团的碳不仅是一种避免热解陷阱的解决方案,而且对于合成方法的发展也具有重要意义。在此,报道了一种液态金属界面工程策略,用于以四氯化碳为碳前驱体、钠钾合金(NaK)为还原剂合成多孔碳,该策略优于传统合成方法,因为它能够构建高活性液态金属合金微乳液,在室温下直接生成多孔碳。所合成的具有丰富碳氯键的多孔碳可以与咪唑和1,2 - 二溴乙烷串联接枝,以获得一种CO环加成催化剂,该催化剂不仅具有出色的稳定性,还表现出优异的催化活性。