High Resolution Image Download MS PowerPoint Slide Selective catalytic oxidation of carbohydrate-derived 5-hydroxymethylfurfural, furfuryl alcohol, and various aromatic and aliphatic compounds to the corresponding aldehyde is a challenging task. The development of a sustainable heterogeneous catalyst is crucial in achieving high selectivity for the desired aldehyde, especially using O 2 or air. In this study, a RuO 2 -supported Mn 3 O 4 catalyst is reported for the selective oxidation reaction. Treatment of MnO 2 molecular sieves with RuCl 3 in aqueous formaldehyde solution gives a new type of RuO 2 -supported Mn 3 O 4 catalyst. Detailed catalyst characterization using powder X-ray diffraction, N 2 adsorption, scanning and transmission electron microscopes, diffuse reflectance UV–visible spectrometer, and X-ray photoelectron spectroscopy proves that the RuO 2 species are dispersed on the highly crystalline Mn 3 O 4 surface. This catalytic conversion process involves molecular oxygen or air (flow, 10 mL/min) as an oxidant. No external oxidizing reagent, additive, or cocatalyst is required to carry out this transformation. This oxidation protocol affords 2,5-diformylfuran, 2-formylfuran, and other aromatic and aliphatic aldehydes in good to excellent yield (70–99%). Moreover, the catalyst is easily recycled and reused without any loss in the catalytic activity.
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Sarmah et al. (2018) studied this question.
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