Related Experiment Video
Updated: Nov 16, 2025

Hydrogen Production and Utilization in a Membrane Reactor
Published on: March 10, 2023
CO2 Activation and Hydrogenation by Palladium Hydride Cluster Anions
Gaoxiang Liu1, Zhaoguo Zhu1, Mary Marshall1
1Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218, United States.
Abstract:
Mass spectrometric analysis of the anionic products of interaction between palladium hydride anions, PdH-, and carbon dioxide, CO2, in a reaction cell shows an efficient generation of the PdHCO2- intermediate and isolated formate product. Multiple isomers of the PdHCO2- intermediates are identified by a synergy between negative ion photoelectron spectroscopy and quantum-chemical calculations. It is shown that a direct mechanism, in which the H atom in PdH- directly activates and hydrogenates CO2, leads to the formation of the formate product. An indirect mechanism, on the other hand, leads to a stable HPdCO2- structure, where CO2 is chemisorbed onto the Pd atom.
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
06:26Achieving Moderate Pressures in Sealed Vessels Using Dry Ice As a Solid CO2 Source
Published on: August 17, 2018
Related Concept Videos
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...
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.
Catalysis
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn stereochemistry.