Related Experiment Video
Updated: Sep 13, 2025

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
Published on: August 17, 2019
Directly Oxidizing Ethanol to Glycolic Acid over a Single-Rh-Site Catalyst via Water-Mediated Oxygen Shuttle
Bin Li1, Jiali Mu1, Guifa Long1,2
1Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Abstract:
Direct oxidation of ethanol to glycolic acid in aqueous solutions under mild conditions offers opportunities for sustainable chemistry. Herein, we report a water-mediated oxygen-shuttle mechanism on S/N/I atoms synergistically coordinated single-Rh-site catalysts (Rh1/AC-SNI400) to enable the direct production of glycolic acid from ethanol oxidation with 93% selectivity in liquid products and a TOF of 250 h-1 at 160 °C. Comprehensive characterizations including isotope labeling experiments and theoretical calculations reveal that hydroxyl radicals (•OH), generated via O2/I-triggered H2O dissociation, insert into C-I bonds to form hydroxyl groups and meanwhile, replace the original OH in ethanol to form C═O, ensuring that all oxygen atoms of glycolic acid directly originate from H2O. O2 enters the system through the decomposition and regeneration of HIO intermediates, completing the oxygen-shuttle cycle driven by sustainable regeneration of water. Furthermore, the optimized S/N/I atoms' synergistical coordination enhances electron delocalization around single-Rh sites, substantially reducing the activation barriers of critical reaction steps and outperforming Rh nanoparticles by 16-fold in activity.
Related Concept Videos
Oxidation of Alcohols
The process of oxidation in a chemical reaction is observed in any of the three forms:
Acid-Catalyzed Dehydration of Alcohols to Alkenes
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...

