Noor Salam

Synthesis of silver–graphene nanocomposite and its catalytic application for the one-pot three-component coupling reaction and one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles in water

A graphene based composite with silver nanoparticles has been synthesized via a simple chemical route and its catalytic activity has been tested for multi-component reactions and click reaction in a one-pot approach. This silver–graphene nanocomposite shows excellent catalytic activity at room temperature for three-component couplings between aldehydes, alkynes and amines (A3-coupling) and one-pot synthesis of 1,4-disubstituted 1,2,3-triazole via click reaction between in situ generated azides (derived from anilines or amines) and terminal acetylenes. This solid silver–graphene catalyst has been characterized by TEM, Raman, XRD and UV-Visible absorption spectra. The developed catalyst is air-stable, inexpensive, easy to prepare and can be facilely recovered and reused five times without significant decrease in activity and selectivity.

Enhanced catalytic performance by copper nanoparticle–graphene based composite

A graphene based composite with copper nanoparticles (Cu–G) has been synthesized and used as catalyst for N-arylation and O-arylation. The structure and composition of the nanocomposite have been characterized by TEM, AFM, Raman and XPS. The catalytic activity of the Cu–G has been tested for the N-arylation of N–H heterocycles using arylboronic acids and the O-arylation of phenols using aryl halides. The catalytic N-arylation produces N-aryl heterocyles and the catalytic O-arylation produces diaryl ethers, under mild reaction conditions with excellent yields and selectivities. The developed catalyst is air-stable, inexpensive, easy to prepare, easy to recover by simple filtration and can be reused without appreciable loss of activity.

Cu-grafted mesoporous organic polymer: a new recyclable nanocatalyst for multi-component, N-arylation and S-arylation reactions

A new mesoporous Cu-MPTA-1 nanocatalyst has been synthesized via a simple and facile in situ radical polymerization of triallylamine in the presence of an organic–organic self-assembly of anionic surfactant SDS, followed by grafting of Cu(II) at room temperature under an inert atmosphere. This nanomaterial has been characterized by elemental analysis, powder X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), UV–vis diffuse reflectance spectroscopy (DRS), thermogravimetric analysis (TGA), N2 adsorption–desorption studies, X-ray photoelectron spectroscopy (XPS) and EPR spectroscopy. Cu-MPTA-1 acts as an efficient heterogeneous nanocatalyst exhibiting a high catalytic activity for N-arylation and S-arylation reactions using water as a green solvent and also exhibits an excellent catalytic activity for the one-pot synthesis of propargylamines via a three component coupling of an alkyne, an amine and an aldehyde at room temperature. Moreover, the catalyst is easily recoverable and can be reused six times without an appreciable loss of catalytic activity in the three component coupling reaction. The highly dispersed Cu(II) sites in the Cu-grafted mesoporous polymer could be responsible for the observed high activities of the Cu-MPTA-1 catalyst in the coupling reactions. No evidence of leached Cu from the catalyst during the course of the reaction has been observed, suggesting true heterogeneity in the catalytic process.

Ag-grafted covalent imine network material for one-pot three-component coupling and hydration of nitriles to amides in aqueous medium

A nitrogen rich porous covalent imine network material (CIN-1) has been successfully employed for grafting silver nanoparticles (Ag NPs). The Ag NPs grafted CIN-1, Ag-CIN-1 has been characterized by elemental analysis, powder X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), UV-vis diffuse reflectance spectroscopy (DRS), thermogravimetric analysis (TGA) and EPR spectroscopic studies. Ag-CIN-1 acts as a truly heterogeneous catalyst in the hydration of nitriles to amides and the A3 coupling reactions between the alkyne, amine and aldehyde to produce propargylamines by using water as a green solvent.

Chromium(VI) grafted mesoporous polyaniline as a reusable heterogeneous catalyst for oxidation reactions in aqueous medium

A new Cr(VI)-grafted mesoporous polyaniline material (Cr-MPANI) has been prepared via simple and facile in situ radical polymerization of aniline followed by reaction with potassium dichromate. This material has been characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), UV-vis diffuse reflectance spectroscopy (DRS) and Thermogravimetric analysis (TGA). Powder XRD and TEM studies suggested the presence of mesophase and disordered wormhole-like mesopores in this sample. Cr-MPANI acts as a very efficient catalyst for the liquid phase oxidation of alkenes, alkanes and aromatic alcohols using 30% H2O2 as oxidant in water. Oxidation reactions were carried out under very mild conditions, and the desired products were obtained with very high selectivity and relatively high yields. Cr-MPANI can be recycled more than five times without an appreciable loss in activity for its respective catalytic reactions.

A highly active recyclable gold–graphene nanocomposite material for oxidative esterification and Suzuki cross-coupling reactions in green pathway

A graphene based composite with gold nanoparticles has been synthesized via a simple chemical route and the structure and compositions of nanocomposite has been characterized. The catalyst was found to be remarkably stable and active for the oxidative esterification of alcohols under present reaction conditions using molecular oxygen as green oxidant and Suzuki cross-coupling reactions between aryl halides and phenylboronic acids using environmentally friendly water as solvent. The versatility of both the protocols was demonstrated by taking a number of substrates. This protocol offers several advantages like high yields, clean reactions, recyclability of the catalyst, reaction in water and use of green oxidant. This study suggests graphene, as an economical substitute for carbon nanotubes, could act as a prominent support in heterogeneous catalysis.

Highly efficient base catalysis and sulfide oxidation reactions over new functionalized mesoporous polymers

Base catalyzed aldol condensation reactions and selective partial oxidation of sulfides are very important classes of reactions in synthetic organic chemistry. We have prepared a new alkali exchanged form of mesoporous polytriallylamine, OH-MPTA-1 and a Cr-grafted material Cr-MPTA-1 via the simple and facile in situ radical polymerization of a triallylamine template by organic–organic self-assembly of anionic surfactant systems. The materials have been characterized by elemental analysis, powder X-ray diffraction (XRD), transmission electron microscope (TEM), Fourier transform infrared spectroscopy (FT-IR), UV-vis diffuse reflectance spectroscopy (DRS), thermogravimetric analysis (TGA) and scanning electron microscopy (SEM). Powder XRD and TEM image analyses suggests the presence of mesophase and disordered wormhole-like mesopores in these samples. Our experimental results reveal that the alkali exchanged material OH-MPTA-1 acts as a very efficient base catalyst for the direct aldol reaction of different aromatic aldehydes with acetone. On the other hand, the Cr-grafted material Cr-MPTA-1, obtained through the reaction of potassium chromate with MPTA-1, acts as a very efficient catalyst for the liquid phase partial oxidation of sulfides to sulfoxides. Both OH-MPTA-1 and Cr-MPTA-1 can be recycled more than five times without an appreciable loss in activity for their respective catalytic reactions.

Cu(II) anchored nitrogen-rich covalent imine network (CuII-CIN-1): an efficient and recyclable heterogeneous catalyst for the synthesis of organoselenides from aryl boronic acids in a green solvent

A new heterogeneous copper catalyst has been synthesized by immobilizing Cu(II) onto the surface of a nitrogen rich porous covalent imine network material CIN-1 and it was characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), EDAX, X-ray photoelectron spectroscopy (XPS), N2 adsorption–desorption, UV-vis spectroscopy, Fourier transform infrared spectroscopy (FT-IR), thermogravimetric (TGA), and EPR spectroscopic analyses. The material has been successfully used to catalyze the cross-coupling reaction between aryl boronic acids and diphenyldiselenide to synthesize unsymmetrical organoselenides. Due to its high surface area and highly accessible catalytic sites, it shows good to excellent catalytic activity for the C–Se bond forming reaction, which was evident from the high TOF of the catalyst in this reaction. The catalyst was recycled for six repetitive runs without any appreciable loss of catalytic activity suggesting its potential usefulness in C–Se bond forming reaction.

Efficient Allylic Oxidation of Olefins Catalyzed by Polymer Supported Metal Schiff Base Complexes with Peroxides

Three homogeneous Cu(II), Co(II) and Ni(II) complexes of a Schiff base ligand and their heterogeneous complexes supported on poly(4-aminostyrene) were prepared and characterized by using elemental analysis, fourier transform infrared spectroscopy, UV–Vis diffuse reflectance spectroscopy, thermogravimetric analysis and scanning electron microscopy. The catalytic performance of both homogeneous and heterogeneous complexes was evaluated in the liquid phase oxidation of cyclohexene, styrene and trans-stilbene in acetonitrile with tert-butylhydroperoxide or hydrogen peroxide as the oxidant. All types of catalyst were active in oxidation; and, the complexes produce allylic oxidation products in all cases. Immobilized complexes are slightly more active than their homogeneous complexes. The polymer-supported Cu(II) complex shows a higher catalytic activity than the other metal species. The activities of the immobilized catalysts remained nearly the same after five cycles, suggesting the true heterogeneous nature of the catalyst.

Polymer-Anchored Cu(II) Complex as an Efficient Catalyst for Selective and Mild Oxidation of Sulfides and Oxidative Bromination Reaction

A new polymer-anchored Cu(II) complex has been tested for the oxidation of sulfides and in oxidative bromination reaction with hydrogen peroxide as oxidant. Sulfides have been selectively oxidized to corresponding sulfoxides in excellent yields and in presence of KBr as bromine source, organic substrates have been selectively converted to mono bromo substituted compounds. The polymer-anchored Cu(II) catalyst could be easily recovered by simple filtration and reused more than six times without appreciable loss of its initial activity.Graphical Abstract