Related Experiment Video
Updated: Sep 15, 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
Catalytic Reduction of Dinitrogen via Hydroboration
Shun Suginome1, Atsushi Okochi1, Taiji Nakamura2
1Department of Applied Chemistry, School of Engineering, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo113-8656, Japan.
Researchers developed a new catalytic method for nitrogen fixation under mild conditions. This process uses molybdenum-nitride catalysts to convert dinitrogen (N₂) into borylamines, offering a promising alternative to the energy-intensive Haber-Bosch process.
Area of Science:
- Inorganic Chemistry
- Catalysis
- Sustainable Chemistry
Background:
- The Haber-Bosch process, essential for ammonia production, requires extreme temperatures and pressures.
- Developing alternative, milder nitrogen fixation methods is crucial for sustainability.
- Catalytic conversion of dinitrogen (N₂) using milder reductants remains a significant challenge.
Purpose of the Study:
- To report a novel catalytic system for the reduction of dinitrogen (N₂) under mild conditions.
- To investigate the hydroboration pathway for N₂ conversion.
- To advance the development of efficient nitrogen fixation technologies.
Main Methods:
- Catalytic reduction of N₂ using catecholborane as a reductant.
- Employing molybdenum-nitride complexes with PCP-type pincer ligands as catalysts.
- Conducting the reaction at 60 °C and 1 atm N₂ pressure.
Main Results:
- Achieved catalytic conversion of N₂ to borylamines with up to 32 equivalents yield.
- The reaction proceeds via successive hydroboration, hydride disproportionation, and N-N bond cleavage.
- Demonstrated the regeneration of the active molybdenum-nitride catalyst.
Conclusions:
- Mild-condition catalytic reduction of N₂ via hydroboration is feasible.
- This method offers a significant advancement over the Haber-Bosch process.
- The developed system represents a step towards ideal nitrogen fixation systems.
Related Concept Videos
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...
Hydroboration-Oxidation of Alkenes
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.
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 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...
Nitriles to Amines: LiAlH4 Reduction
As shown below, the mechanism involves three steps. Firstly, the hydride ion acting as a nucleophile attacks the nitrile carbon to form an anion. In the second step, a second equivalent of the hydride ion attacks the anion to...

