Related Experiment Video
Updated: Aug 22, 2026

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
Bootstrap Synthesis Revisited: A Solid, Cobalt-Derived Catalyst Enables the Hydrogenation of NN Bonds to Afford
Fabian Schmiedbauer1, Jiri Duchoslav2, Laura Zellner3
1Institute of Inorganic Chemistry, Johannes Kepler University (JKU), Linz 4040, Austria.
Abstract:
We communicate a solvent-free and low-waste method for the fabrication of a heterogeneous, Co-based hydrogenation catalyst. Careful pyrolysis of a solid [Co-(acac)2]/phthalocyanine/Vulcan mixture (acac = acetylacetonate) under an argon atmosphere furnishes a ready-to-use, catalytically active material that can be handled without any protection from air. The composite so obtained was then used in the pressure hydrogenation of azo dyes (60 °C, 50 bar H2) to yield the corresponding aniline derivatives, without any additive. The potential of the catalyst to design a bootstrap synthesis approach of aromatic amines, i.e., their generation from within themselves, by way of reduction of symmetric azo compounds is explored herein, too. To further demonstrate the practicality of the introduced catalyst, we also applied it to the hydrogenation of nitroarenes as another means for the production of arylamines. In all investigated cases, the NO2 motif was neatly and selectively converted into the desired NH2 group under very mild reaction conditions (room temperature, 20 bar H2) and, again, without the need for any auxiliary reagents.
More Related Videos
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
12:27Synthesis of Hypervalent Iodonium Alkynyl Triflates for the Application of Generating Cyanocarbenes
Published on: September 8, 2013
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...
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.
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
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 surface of...
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
Catalysis