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通过甲酰化实现CO加氢制备高选择性N,N-二甲基甲酰胺的可控活性中间体

Controllable Active Intermediate in CO Hydrogenation Enabling Highly Selective ,-Dimethylformamide Synthesis via -Formylation.

作者信息

Zhang Jieyun, Li Guanna, Xie Jin, Hai Yang, Wan Weiming, Sun Haotian, Wang Bin, Wu Xiaojing, Cheng Jiannian, He Changxin, Hu Wei, Zhang Ying, Li Zelong, Li Can

机构信息

Key Laboratory of Advanced Catalysis, Gansu Province, State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, Gansu 730000, China.

Biobased Chemistry and Technology Group, Wageningen University, Bornse Weilanden 9, 6708 WG Wageningen, The Netherlands.

出版信息

J Am Chem Soc. 2025 Jan 29;147(4):3152-3160. doi: 10.1021/jacs.4c12503. Epub 2024 Dec 19.

DOI:10.1021/jacs.4c12503
PMID:39700414
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11783538/
Abstract

,-Dimethylformamide (DMF) is a widely used solvent, and its green and low-carbon synthesis methods are in high demand. Herein, we report a new approach for DMF synthesis using a continuous flow reaction system with a fixed-bed reactor and a ZnO-TiO solid solution catalyst. This catalyst effectively utilizes CO, H, and dimethylamine (DMA) as feedstocks, demonstrating performance with 99% DMF selectivity and single-pass DMA conversion approaching thermodynamic equilibrium. Moreover, the catalyst demonstrates good stability, with no signs of deactivation over 1000 h of continuous operation. The key to superior activity lies in the synergetic effect of the Zn and Ti sites, which facilitates the formation of active formate species. These species act as crucial intermediates, reacting with DMA to produce DMF. Importantly, the slow hydrogenation kinetics of the formate species prevent the formation of CHO* species, thereby suppressing the formation of the undesired byproduct, trimethylamine. This work underscores the potential of kinetically controlling active intermediates in CO hydrogenation to prepare high-value-added chemicals by coupling them to platform molecules. It presents a promising strategy for the efficient utilization of CO resources and offers a valuable solution for large-scale DMF synthesis.

摘要

N,N-二甲基甲酰胺(DMF)是一种广泛使用的溶剂,其绿色低碳合成方法备受关注。在此,我们报道了一种利用固定床反应器和ZnO-TiO固溶体催化剂的连续流动反应体系合成DMF的新方法。该催化剂有效利用CO、H₂和二甲胺(DMA)作为原料,DMF选择性达99%,单程DMA转化率接近热力学平衡。此外,该催化剂表现出良好的稳定性,连续运行1000小时无失活迹象。优异活性的关键在于Zn和Ti位点的协同作用,这有利于活性甲酸盐物种的形成。这些物种作为关键中间体,与DMA反应生成DMF。重要的是,甲酸盐物种缓慢的氢化动力学阻止了CHO*物种的形成,从而抑制了副产物三甲胺的生成。这项工作强调了在CO加氢反应中通过动力学控制活性中间体,将其与平台分子偶联合成高附加值化学品的潜力。它为CO资源的高效利用提供了一种有前景的策略,并为大规模DMF合成提供了有价值的解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89ce/11783538/3d82bd383824/ja4c12503_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89ce/11783538/e330befde37a/ja4c12503_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89ce/11783538/271df6e2e867/ja4c12503_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89ce/11783538/ba0ad495a7b0/ja4c12503_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89ce/11783538/e72cc0537661/ja4c12503_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89ce/11783538/3d82bd383824/ja4c12503_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89ce/11783538/e330befde37a/ja4c12503_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89ce/11783538/271df6e2e867/ja4c12503_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89ce/11783538/ba0ad495a7b0/ja4c12503_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89ce/11783538/e72cc0537661/ja4c12503_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89ce/11783538/3d82bd383824/ja4c12503_0005.jpg

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本文引用的文献

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J Am Chem Soc. 2023 Jun 14;145(23):12663-12672. doi: 10.1021/jacs.3c02248. Epub 2023 Jun 1.
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Flame-made ternary Pd-InO-ZrO catalyst with enhanced oxygen vacancy generation for CO hydrogenation to methanol.
火焰制备的具有增强氧空位生成能力的三元Pd-InO-ZrO催化剂用于CO加氢制甲醇
Nat Commun. 2022 Sep 24;13(1):5610. doi: 10.1038/s41467-022-33391-w.
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Highly Efficient and Selective N-Formylation of Amines with CO and H Catalyzed by Porous Organometallic Polymers.多孔有机金属聚合物催化CO和H对胺进行高效选择性N-甲酰化反应
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