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The efficient CO2 fixation catalyzed by K-doped g-C3N4 catalyst for synthesizing benzimidazoles at atmospheric pressure
Greenhouse Gases: Science and Technology ( IF 2.2 ) Pub Date : 2023-05-31 , DOI: 10.1002/ghg.2222
Xuewei Tu 1 , Luping Zhang 1 , Yutong Chen 1 , Shouxin Zhu 1 , Can Sun 1 , Jiali Jin 1 , Min Liu 1 , Hui Zheng 1
Affiliation  

The conversion of CO2 into valuable chemicals to reduce greenhouse gas emissions has received extensive attention. Converting CO2 into pharmaceutical intermediates via graphitic carbon nitride (CN) at atmospheric pressure is a challenge. In this work, a series of novel graphitic carbon nitrides (K-CN) catalysts with different doping ratios of K were synthesized by post-treatment of CN with KOH as a dopant under magnetic stirring. Herein, substrates of o-phenylenediamine with different electron-donating/withdrawing groups were employed to convert CO2 into high-value heterocyclic benzimidazoles. The optimal reaction conditions were determined by a single factor optimization approach. A series of benzimidazole derivatives were synthesized with a yield of up to 96% under atmospheric pressure, indicating that the catalyst can efficiently fix CO2. This work not only designs a simple and low-cost K-CN catalyst but also provides a new pathway for converting CO2 into valuable benzimidazole derivatives at atmospheric pressure. © 2023 Society of Chemical Industry and John Wiley & Sons, Ltd.

中文翻译:

K掺杂g-C3N4催化剂催化高效固定CO2常压合成苯并咪唑

将CO 2转化为有价值的化学品以减少温室气体排放已受到广泛关注。在大气压下通过石墨氮化碳(CN)将CO 2转化为医药中间体是一个挑战。本工作以KOH为掺杂剂在磁力搅拌下对CN进行后处理,合成了一系列不同K掺杂比例的新型石墨氮化碳(K-CN)催化剂。在此,采用具有不同给电子/吸电子基团的邻苯二胺底物来转化CO 2转化为高价值的杂环苯并咪唑。通过单因素优化方法确定最佳反应条件。在常压下合成了一系列苯并咪唑衍生物,收率高达96%,表明该催化剂能够有效固定CO 2。这项工作不仅设计了一种简单、低成本的K-CN催化剂,而且为常压下将CO 2转化为有价值的苯并咪唑衍生物提供了一条新途径。© 2023 化学工业协会和 John Wiley & Sons, Ltd.
更新日期:2023-05-31
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