Herein, we report a general and straightforward synthesis method for gold supported on mesoporous and microporous metal oxides. Supported materials, in general, show higher crystallinity compare to unsupported systems as verified through powder X-ray diffraction (XRD). Also, through XRD, most of the metal is observed to be in its oxide form, whereas the gold support was found to be in its metallic state, which has been further confirmed from TEM. In terms of surface area, the catalyst was not found to follow any trend. Morphology wise, there are no changes observed after doping except in few cases. Combined results from XRD, X-ray fluorescence spectroscopy, Auger, and X-ray photoelectron spectroscopy suggest that gold is mainly in the bulk and very little (0.04% in case of gold doped calcium oxide) or non (in case of gold doped mixed manganese-cerium oxide) on the surface. The presence of Au (0) 4f peaks in XPS further confirms the metallic state of the gold. Oxides of indium, magnesium and calcium have been studied for the organic transformation reactions. An enhancement in activity and product selectivity was observed in the case of the gold supported catalysts. Indium serves as a great catalyst for C–C coupling and electrophilic aromatic substitution reactions and gives >99% conversion. Interestingly, 88% selectivity for C–C coupling and >99% selectivity for aromatic substitution have been achieved at 100 °C and room temperature respectively. Magnesium and calcium give Knoevenagel condensation products. At room temperature with very low catalyst loading, >99% conversion and selectivity were observed for the Knoevenagel reaction with as high as 35.30 TOF. A mechanism for the C–C coupling reaction has been proposed based on these results. The general and straightforward synthesis of gold promoted mesoporous and microporous metal oxides were templated using Pluronic P123 surfactant via inverse micelle formation. These catalysts were scanned for the various organic transformation reactions and enhanced activity was shown in the case of gold promoted catalysts. • A general and straightforward synthesis method for gold support mesoporous and microporous metal oxides. • An improvement in metal oxide crystallinity as a result of gold doping. • An enhancement in activity and product selectivity due to the gold supported catalysts. • Indium based C–C coupling and electrophilic aromatic substitution reactions that give >99% conversion. • High selectivity and high conversion for Knoevenagel ester condensation with very low catalyst loading.
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