Hydrogen is an important resource for realizing the goal of a hydrogen-based society as well as for synthetic organic chemistry. Catalytic dehydrogenation of organic hydrides such as methyl cyclohexane is attractive for hydrogen storage and transportation in terms of reversibility and selectivity of catalytic reactions and hydrogen storage density. We developed a highly active polymethylphenylsilane-aluminum immobilized platinum catalyst (Pt/MPPSi-Al2 O3 ) for dehydrogenation of organic hydrides. Organic hydrides were fully converted into the corresponding aromatic compounds under reactive distillation conditions at 200 °C or under circulation-flow conditions using the Pt/MPPSi-Al2 O3 catalyst packed in a column at 260 °C. The dehydrogenation reaction reached a maximum conversion at equilibrium (ca. 60%) under continuous-flow conditions at 260 °C. This catalytic continuous-flow dehydrogenation was applied to a formal hydrogen transfer from organic hydrides to unsaturated organic substrates under sequential and continuous-flow conditions for practical flow hydrogenation reactions by connecting two different heterogeneous catalysts packed in columns.
Keywords: Dehydrogenation of organic hydrides; Flow reactor; Heterogeneous catalysis; Metal nanoparticle; hydrogenation.
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