Preparation and characterization of nickel aluminosilicate nanocomposites for transfer hydrogenation of carbonyl compounds

Three different samples of nickel aluminosilicate (NAS) nanocomposite for application as catalyst in transfer hydrogenation reactions were prepared by the incorporation of nickel nanoparticles into the mesoporous aluminosilicate framework obtained by a simple sol–gel method followed by calcinations at various temperatures without using any templates. The above prepared nanocomposites were characterized using thermal studies, Fourier transform infrared (FT-IR) spectroscopy, powder X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDAX), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and nitrogen adsorption–desorption (BET) analysis. Effect of calcination temperature of alumnosilicate support on the surface area and pore size of the nanocomposites was studied from BET analysis. Crystalline nature and particle size of nickel oxide present in the aluminosilicate framework was determined from powder XRD pattern. Surface morphology of the catalysts and their elemental compositions were obtained from SEM and EDAX techniques, respectively. Catalytic activity of the above prepared catalysts towards transfer hydrogenation (TH) of carbonyl compounds using isopropyl alcohol as hydrogen donor in presence of KOH was tested with wide range of carbonyl compounds. The yield of the products formed in TH reaction was monitored by gas chromatography (GC).

Graphical abstractNickel aluminosilicate nanocomposite prepared by sol–gel technique was used for the transfer hydrogenation of carbonyl compounds.Figure optionsDownload full-size imageDownload high-quality image (112 K)Download as PowerPoint slideHighlights► Nickel aluminosilicate nanocomposites were prepared by sol–gel technique and characterized by various physiochemical techniques. ► Transfer hydrogenation of carbonyl compounds were carried out using the prepared catalyst. ► 2-Chloro-3-formyl quinoline and its derivatives were reduced to their corresponding alcohols in excellent yield.