Related Experiment Video
Updated: Sep 24, 2025

Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
Published on: December 6, 2021
Nitrogen-Doped Carbon as a Highly Active Metal-Free Catalyst for the Selective Oxidative Dehydrogenation of
Xun Li1, Ziliang Yuan1,2, Yi Liu3
1Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education, South-Central Minzu University, Wuhan, 430074, P. R. China.
Abstract:
N-heteroarenes represents one of the most important chemicals in pharmaceuticals and other bio-active molecules, which can be easily accessed from the oxidation of N-heterocycles over metal catalysts. Herein, the metal-free oxidative dehydrogenation of N-heterocycles into N-heteroarenes was developed using molecular oxygen as the terminal oxidant. The nitrogen-doped carbon materials were facilely prepared via the simple pyrolysis process using biomass (carboxymethyl cellulose sodium) and dicyandiamide as the carbon and nitrogen source, respectively, and they were discovered to be robust for the oxidative dehydrogenation of N-heterocycles into N-heteroarenes under mild conditions (80 °C under 1 bar O2 ) with water as the green solvent. Diverse N-heterocycles including 1,2,3,4-tetrahydroisoquinolines, indolines and 1,2,3,4-tetrahydroquinoxalines were smoothly converted into N-heteroarenes with high to excellent yields (76->99 %). Superoxide radical (⋅O2 - ) and hydroxyl radical (⋅OH) were probed as the reactive oxygen species for the oxidation of N-heterocycles into N-heteroarenes. More importantly, the nitrogen-doped carbon catalyst can be reused with a high stability. The method provides an environmentally friendly and economical route to access important N-hetero-aromatic commodities.
More Related Videos
10:57Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
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
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Catalysis
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Preparation of Amines: Reduction of Oximes and Nitro Compounds
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...