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通过原子分散的负载铁缺陷TiO上的电催化C-N偶联反应高效合成α-氨基酸

Highly Efficient Synthesis of α-Amino Acids via Electrocatalytic C-N Coupling Reaction Over an Atomically Dispersed Iron Loaded Defective TiO.

作者信息

Zhu Zhonghuan, Jiang Yimin, Xu Leitao, An Qizheng, Nga Ta Thi Thuy, Chen Junlin, Fan Yun, Liu Qinghua, Dong Chung-Li, Wang Shuangyin, Zou Yuqin

机构信息

State Key Laboratory of Chem/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan, 410082, P. R. China.

National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, 230029, P. R. China.

出版信息

Adv Mater. 2025 Feb;37(5):e2409864. doi: 10.1002/adma.202409864. Epub 2024 Dec 12.

Abstract

The synthesis of α-amino acids via the electrocatalytic C-N coupling attracted extensive attention owing to the mild reaction conditions, controllable reaction parameters, and atom economy. However, the α-amino acid yield remains unsatisfying. Herein, the efficient electrocatalytic synthesis of α-amino acids is achieved with an atomically dispersed Fe loaded defective TiO monolithic electrocatalyst (Fe-TiO/Ti). The desired electrocatalyst composition for the hydrogenation of oxime is screened. The prepared Fe-TiO/Ti exhibited a high glyoxylic acid conversion of ≈100% and a glycine selectivity of 80.2%. The electrochemical experiments and theoretical calculations demonstrated that atomically dispersed Fe (Fe) sites and oxygen vacancies (OVs) enhanced the adsorption of glyoxylic acid (GA), glyoxylic oxime (GO), and nitrate (NO ). Fe sites further promote the step of HNO → HNOH in the conversion of NO to hydroxylamine (NHOH) and the step of NH-CH-COOH → NH-CH-COOH in the reduction of GO to glycine. The coupling pathway and the critical intermediate are revealed by synchrotron radiation Fourier transform infrared (SR-FTIR) spectroscopy and differential electrochemical mass spectrometry (DEMS). Additionally, six other α-amino acids are successfully synthesized by the Fe-TiO/Ti, showcasing its versatility in the electrosynthesis of α-amino acids. This work provides an efficient electrocatalyst for the C-N coupling synthesis of α-amino acids.

摘要

通过电催化C-N偶联合成α-氨基酸由于反应条件温和、反应参数可控以及原子经济性而受到广泛关注。然而,α-氨基酸的产率仍然不尽人意。在此,使用原子分散的负载铁的缺陷TiO整体式电催化剂(Fe-TiO/Ti)实现了α-氨基酸的高效电催化合成。筛选出了用于肟氢化的理想电催化剂组成。制备的Fe-TiO/Ti表现出约100%的高乙醛酸转化率和80.2%的甘氨酸选择性。电化学实验和理论计算表明,原子分散的Fe(Fe)位点和氧空位(OVs)增强了乙醛酸(GA)、乙醛酸肟(GO)和硝酸盐(NO )的吸附。Fe位点进一步促进了NO 转化为羟胺(NHOH)过程中HNO → HNOH这一步骤以及GO还原为甘氨酸过程中NH-CH-COOH → NH-CH-COOH这一步骤。通过同步辐射傅里叶变换红外(SR-FTIR)光谱和差分电化学质谱(DEMS)揭示了偶联途径和关键中间体。此外,Fe-TiO/Ti成功合成了其他六种α-氨基酸,展示了其在α-氨基酸电合成中的通用性。这项工作为α-氨基酸的C-N偶联合成提供了一种高效的电催化剂。

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