Related Experiment Video
Updated: Aug 16, 2025

Preparation of Polyoxometalate-based Photo-responsive Membranes for the Photo-activation of Manganese Oxide Catalysts
Published on: August 7, 2018
Salt-templated porous melamine-based conjugated polymers for selective oxidation of amines into imines under visible
Feng Chu1, Yezi Hu2, Kaiyue Zhang1
1Beijing Advanced Innovation Center for Materials Genome Engineering, Beijing Key Laboratory of Function Materials for Molecule & Structure Construction, School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083, PR China.
Abstract:
Conjugated polymers have a broad application foreground in the field of photocatalytic organic synthesis to produce value-added chemicals due to their functional diversity, broad light responsive ability, high thermal and chemical stability, and tunable band structure. Herein, using mixed chloride salts (i.e., NaCl/LiCl) as building template, a series of porous conjugated polymers constructed by melamine and terephthalaldehyde monomers were obtained through a Schiff-base reaction in the absence of any external solvent. Melamine-terephthalaldehyde polymer (i.e., PMTPA-x, x represents the mass ratio of salt-mixture to mixed precursors of PMTPA) materials displayed porous morphologies and possessed different energy band structures via regulating the mass ratio of mixed-salt to monomers. Specifically, PMTPA-20 has a larger specific surface area and more suitable redox potential towards the photocatalytic oxidative coupling of amines to imines. Under visible light, with molecular oxygen as oxidant, PMTPA-20 achieves 97% conversion of benzylamine in 8 h which is 3.9 times higher than that of pristine PMTPA (25% conversion in 8 h). In addition, PMTPA-20 catalyst has good structure stability and reusability performance for photocatalytic reactions.
Related Concept Videos
Aldehydes and Ketones with Amines: Imine and Enamine Formation Overview
Aldehydes and Ketones with Amines: Imine Formation Mechanism
Imines are formed under mildly acidic conditions. A pH of 4.5 is ideal for the reaction.
If the pH is low or the solution is too acidic, the reaction slows down in the...
Preparation of Amines: Reduction of Oximes and Nitro Compounds
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
Amines to Amides: Acylation of Amines
Next, the second equivalent of amine serves as a Brønsted base and deprotonates the quaternary...
Preparation of 1° Amines: Azide Synthesis
Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...
Preparation of Amines: Reductive Amination of Aldehydes and Ketones
![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)
![Solid-phase Synthesis of [4.4] Spirocyclic Oximes](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F58508.jpg&w=3840&q=50)