Related Experiment Video
Updated: Jul 26, 2026

Fabrication of Spatially Confined Complex Oxides
Published on: July 1, 2013
Selective oxidation of styrene on an oxygen-covered Au(111)
Xingyi Deng1, Cynthia M Friend
1Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, USA.
Abstract:
For the first time, we demonstrate olefin epoxidation promoted by an extended Au surface. The oxidation of styrene to styrene epoxide, benzoic acid, and benzeneacetic acid is promoted on Au(111) covered with 0.2 ML of oxygen atoms. The estimated selectivity for styrene epoxide formation is approximately 53%. Total combustion to CO2 accounts for approximately 20% of the styrene reaction. We propose that styrene epoxide, benzoic acid, and benzeneacetic acid are produced via two possible oxametallacycle intermediates. Our work demonstrates that extended Au is an effective material for olefin oxidation, which has implications for understanding the activity of nanoscale Au catalysts.
More Related Videos
06:30Fabrication of Ultra-thin Color Films with Highly Absorbing Media Using Oblique Angle Deposition
Published on: August 29, 2017
12:08Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
Published on: June 24, 2022
Related Concept Videos
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.