Related Experiment Video
Updated: Jan 18, 2026

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Molecular functionalization of Ni(OH)2 promotes electrosynthesis of adipic acid
Rui Yang1, Yuanhao Li2, Haonan Xu3
1Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering, State Key Laboratory of Synergistic Chem-Bio Synthesis, Zhangjiang Institute for Advanced Study, Shanghai Jiao Tong University Shanghai 200240 China sunyf@sjtu.edu.cn.
Abstract:
Adipic acid is an essential platform molecule for polymer production and is industrially manufactured by thermochemical oxidation of the cyclohexanone/cyclohexanol mixture (KA oil). Alternatively, electrifying provides a green and sustainable route to synthesizing adipic acid, but has been restricted by the low catalytic efficiency. Herein, we report that a nickel hydroxide electrocatalyst functionalized with 4,4'-bipyridine (Bipy-Ni(OH)2) delivers a 3-fold greater productivity compared with that of pristine Ni(OH)2, achieving an excellent yield (90%) towards efficient adipic acid electrosynthesis. The experimental and molecular dynamics (MD) simulation results show that Bipy serves as a reservoir to accumulate cyclohexanone, which has low solubility in aqueous solutions. Molecular probe analysis coupled with density functional theory (DFT) calculations demonstrates that Bipy functionalization promotes formation of the key intermediate (2-hydroxycyclohexanone) via modulating the surface electronic characteristics. A Bipy-Ni(OH)2//Ru electro-reforming system in a two-electrode configuration was further constructed to enable concurrent hydrogen and adipate production, revealing its potential for practical applications. Our report demonstrates the efficacy of grafting judicious ligands to electrocatalysts to harness mass transfer and optimize active sites, and the insights can be useful for electrooxidation of a wider scope of organic molecules.
More Related Videos
Related Concept Videos
Oxidations of Aldehydes and Ketones to Carboxylic Acids
Aldehydes readily undergo oxidation in strong oxidizing agents such as potassium permanganate and chromic acid. The oxidation can also be carried out using mild oxidizing agents such as silver oxide. In fact, aldehydes can be easily oxidized...
Preparation of Carboxylic Acids: Hydrolysis of Nitriles
Nucleophilic Addition to the Carbonyl Group: General Mechanism
A stronger nucleophile can directly attack the electrophilic center, the carbonyl carbon. The HOMO orbital of the nucleophile interacts with the LUMO (π* antibonding) orbital present on the carbonyl carbon. This interaction breaks the π bond and shifts the π...
Nitriles to Amines: LiAlH4 Reduction
As shown below, the mechanism involves three steps. Firstly, the hydride ion acting as a nucleophile attacks the nitrile carbon to form an anion. In the second step, a second equivalent of the hydride ion attacks the anion to...
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Nitriles to Carboxylic Acids: Hydrolysis

