Related Experiment Video
Updated: May 13, 2025

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
Published on: October 18, 2019
Highly Active and Air-Stable Iron Phosphide Catalyst for Reductive Amination of Carbonyl Compounds Enabled by
Tomohiro Tsuda1, Hiroya Ishikawa1, Min Sheng1
1Department of Materials Engineering Science, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama, Toyonaka, Osaka 560-8531, Japan.
Abstract:
Iron has long been recognized as an ideal catalytic material for sustainable chemistry. However, conventional iron catalysts employed in liquid-phase hydrogenation reactions suffer from poor activity and air instability, severely restricting their wide applicability in practical use. Herein, we present the development of highly active and air-stable iron phosphide nanocrystal immobilized on zirconia (Fe2P NC/ZrO2) for the reductive amination of aldehydes and ketones. The Fe2P NC/ZrO2 catalyst demonstrated broad substrate applicability, high recyclability, and scalability in both gram-scale and continuous-flow processes. This catalyst leverages the synergistic metal-support effect of Fe2P NCs and ZrO2 support, leading to activity 313 times higher than that of conventional iron nanoparticle catalysts. In-depth mechanistic studies elucidated that the distinctive interplay between Fe2P and ZrO2 significantly accelerates ammonolysis of Schiff bases, a key step for boosting reaction efficiency. This study sets a new benchmark for iron-based catalysis, offering a robust alternative to precious metals, thereby contributing significantly to sustainable chemical manufacturing and green organic synthesis.
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
14:07Preparation and Use of Carbonyl-decorated Carbenes in the Activation of White Phosphorus
Published on: October 3, 2014
Related Concept Videos
Preparation of Amines: Reductive Amination of Aldehydes and Ketones
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.
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...
Amides to Amines: LiAlH4 Reduction
Amide reduction requires two equivalents of the reducing agent, acting as a source of hydride ions. As shown in the figure, the reaction is initiated with a nucleophilic attack by the hydride ion at the carbonyl carbon to form a tetrahedral intermediate.
Preparation of Amines: Reduction of Amides and Nitriles
Amides can be reduced to primary, secondary, and tertiary amines using catalytic hydrogenation, active metals like Fe,...