Borane cluster-based porous covalent networks, named activated borane (), were prepared by cothermolysis of decaborane(14) (-BH) and selected hydrocarbons (toluene, cyclohexane, ; and -hexane, ) under anaerobic conditions. These amorphous solid powders exhibit different textural and Lewis acid (LA) properties that vary depending on the nature of the constituent organic linker. For , its LA strength even approaches that of the commonly used molecular LA, B(CF). Most notably, s can act as heterogeneous LA catalysts in hydrosilylation/deoxygenation reactions with various carbonyl substrates as well as in the gas-phase dehydration of ethanol. These studies reveal the potential of s in catalytic applications, showing (a) the possibility for tuning catalytic reaction outcomes (selectivity) in hydrosilylation/deoxygenation reactions by changing the material's composition and (b) the very high activity toward ethanol dehydration that exceeds the commonly used γ-AlO by achieving a stable conversion of ∼93% with a selectivity for ethylene production of ∼78% during a 17 h continuous period on stream at 240 °C.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10660343PMC
http://dx.doi.org/10.1021/acscatal.3c04011DOI Listing

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Borane cluster-based porous covalent networks, named activated borane (), were prepared by cothermolysis of decaborane(14) (-BH) and selected hydrocarbons (toluene, cyclohexane, ; and -hexane, ) under anaerobic conditions. These amorphous solid powders exhibit different textural and Lewis acid (LA) properties that vary depending on the nature of the constituent organic linker. For , its LA strength even approaches that of the commonly used molecular LA, B(CF).

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