Programmable Mono‐/Di‐alkylation of Amines with Aldehydes Over a Pd <i> <sup>δ</sup> </i> <sup>−</sup> –H Electrocatalyst

Abstract Programmable amine N‐alkylation provides a new method to combine the required alkyl groups with amine molecules according to actual demand and to precisely regulate the biological and pharmaceutical properties of life science amine molecules. However, only the electrochemical mono‐methylation of amines has been achieved via C─N coupling with CO 2 accompanied by an unsatisfactory Faraday efficiency (FE) lower than 10%. Herein, we developed programmable electrocatalytic N‐alkylation of amines with two controllable alkyl groups and one methyl group. Both experimental characterization and density functional theory (DFT) calculations have demonstrated the critical role of electron‐enriched Pd metals in transforming amines into alkylamines with two chosen alkyl groups and a methyl group. Moreover, the electrocatalytic transformation of amines to alkylamines with satisfactory FE values (86%–96%) has been achieved, further expanding the scope of electrochemical C─N coupling and possibly opening a new world of electrochemical amine N‐alkylation.

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Publication Details

Journal
Angewandte Chemie
Published
2025-03-18
DOI
https://doi.org/10.1002/ange.202425622
Citations
1
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.54
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Programmable Mono‐/Di‐alkylation of Amines with Aldehydes Over a Pd δ − –H Electrocatalyst

Kai-Yuan Lu, Jie‐Sheng Chen, Shi‐Nan Zhang, Bing‐Liang Leng et al.
1 citations
Angewandte Chemie
Asymmetric Hydrogenation and Catalysis
0.54
article

Programmable Mono‐/Di‐alkylation of Amines with Aldehydes Over a Pd δ − –H Electrocatalyst

Kai-Yuan Lu, Jie‐Sheng Chen, Shi‐Nan Zhang, Bing‐Liang Leng, Xin‐Hao Li, Dong Xu, Siyuan Xia
article en
1 citations

Abstract

Abstract Programmable amine N‐alkylation provides a new method to combine the required alkyl groups with amine molecules according to actual demand and to precisely regulate the biological and pharmaceutical properties of life science amine molecules. However, only the electrochemical mono‐methylation of amines has been achieved via C─N coupling with CO 2 accompanied by an unsatisfactory Faraday efficiency (FE) lower than 10%. Herein, we developed programmable electrocatalytic N‐alkylation of amines with two controllable alkyl groups and one methyl group. Both experimental characterization and density functional theory (DFT) calculations have demonstrated the critical role of electron‐enriched Pd metals in transforming amines into alkylamines with two chosen alkyl groups and a methyl group. Moreover, the electrocatalytic transformation of amines to alkylamines with satisfactory FE values (86%–96%) has been achieved, further expanding the scope of electrochemical C─N coupling and possibly opening a new world of electrochemical amine N‐alkylation.

Angewandte ChemieVol. 137(22)
Shanghai Jiao Tong University (CN)
Openalex Percentile: Top 38%
Asymmetric Hydrogenation and Catalysis
0.54
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Programmable Mono‐/Di‐alkylation of Amines with Aldehydes Over a Pd <i> <sup>δ</sup> </i> <sup>−</sup> –H Electrocatalyst — Kai-Yuan Lu, Jie‐Sheng Chen, et al. · Angewandte Chemie (2025) | TGRS Research Map | TGRS