Related Experiment Video
Updated: Sep 27, 2025

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
Published on: July 30, 2017
Tridimensional N, P-Codoped Carbon Sponges as Highly Selective Catalysts for Aerobic Oxidative Coupling of
Lu Peng1, Herme G Baldovi1, Amarajothi Dhakshinamoorthy2
1Instituto Universitario de Tecnología Química, Consejo Superior de Tecnología Química-Universitat Politècnica de Valencia, Av. De los Naranjos s/n, 46010 Valencia, Spain.
Abstract:
Two tridimensional N-doped porous carbon sponges (3DC-X) have been prepared by using cetyltrimethylammonium chloride (CTAC) and cetyltrimethylammonium bromide (CTAB) as soft templates and alginate to replicate the liquid crystals formed by CTA+ in water. Alginate is a filmogenic polysaccharide of natural origin having the ability to form nanometric defectless films around objects. Subsequent pyrolysis at 900 °C under an Ar flow of the resulting CTA+-polysaccharide assemblies result in 3DC-1 and 3DC-2, with the N percentages of 0.48 and 0.36 wt % for the materials resulting from CTAC and CTAB, respectively. Another four 3DC materials were obtained via pyrolysis of the adduct of phytic acid and chitosan, rendering an amorphous, N and P-codoped carbon sample (3DC-3 to 3DC-6). The six 3DC samples exhibit a large area (>650 m2 × g-1) and porosity, as determined by Ar adsorption. The catalytic activity of these materials in promoting the aerobic oxidation of benzylamine increases with the specific surface area and doping, being the largest for 3DC-4, which is able to achieve 73% benzylamine conversion to N-benzylidene benzylamine in solventless conditions at 70 °C in 5 h. Quenching studies and hot filtration tests indicate that 3DC-4 acts as a heterogeneous catalyst rather than an initiator, triggering the formation of hydroperoxyl and hydroxyl radicals as the main reactive oxygen species involved in the aerobic oxidation.
More Related Videos
11:44Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions
Published on: March 20, 2014
09:12[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
Published on: May 21, 2019
Related Concept Videos
Electrophilic Aromatic Substitution: Nitration of Benzene
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...
Electrophilic Aromatic Substitution: Sulfonation of Benzene
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism
Nucleophilic Aromatic Substitution: Elimination–Addition