Suppr超能文献

通过阴阳极串联电解槽将羟基和硝酸盐共同升级为肟。

Hydroxyl and nitrate co-upgrading to oxime via anode-cathode cascade electrolyzer.

作者信息

Peng Ouwen, Hu Qikun, Jin Mengtian, Su Mengyao, Liu Jia, Li Bo, Xi Shibo, Cheng Chun, Loh Kian Ping

机构信息

Department of Materials Science and Engineering, Southern University of Science and Technology, Shenzhen, 518055, China.

Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore, Singapore.

出版信息

Nat Commun. 2025 Jul 3;16(1):6145. doi: 10.1038/s41467-025-61186-2.

Abstract

Oximes are crucial intermediates in the production of polymers and pharmaceuticals. Conventional synthesis methods, involving the hydrogenation of nitrogen oxides and nucleophilic addition of hydroxylamine to carbonyl compounds, are energy-intensive and hazardous. Here, we report an economical and sustainable electrosynthesis route to oximes using hydroxyl compounds and nitrate in an anode-cathode cascade electrolyzer. In this system, hydroxyl compounds are first dehydrogenated to ketones at a cobalt oxyhydroxide anode, followed by the subsequent co-reduction of ketones with nitrate at a Cu-substituted FeC cathode to form oximes. The cascade electrolyzer exhibits robust performance over 72 h at 2.8 V, achieving a high pyruvatoxime yield of 2.61 mmol cm h with a Faradaic efficiency of 101%. This versatile method accommodates diverse feedstocks, enabling the production of various relevant commodities. Process modeling and techno-economic analysis confirm the viability and cost-effectiveness of this innovative approach, offering a more sustainable pathway to essential chemical intermediates.

摘要

肟是聚合物和药物生产中的关键中间体。传统的合成方法,包括氮氧化物的氢化以及羟胺对羰基化合物的亲核加成,能源消耗大且具有危险性。在此,我们报道了一种经济且可持续的电合成肟的路线,该路线在阴阳极串联电解槽中使用羟基化合物和硝酸盐。在这个体系中,羟基化合物首先在氢氧化氧钴阳极上脱氢生成酮,随后酮在铜取代的FeC阴极上与硝酸盐共同还原形成肟。该串联电解槽在2.8 V电压下72小时内表现出稳健的性能,丙酮酸肟产率高达2.61 mmol cm h,法拉第效率为101%。这种通用方法适用于多种原料,能够生产各种相关产品。过程建模和技术经济分析证实了这种创新方法的可行性和成本效益,为重要化学中间体提供了一条更具可持续性的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee63/12229646/ca223674a7de/41467_2025_61186_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验