Porous Magnesium Oxide by Twin Polymerization: From Hybrid Materials to Catalysis


Porous Magnesium Oxide by Twin Polymerization: From Hybrid Materials to Catalysis

Scharf, S.; Notz, S.; Thomas, R.; Mehring, M.; Tegenkamp, C.; Formánek, P.; Hübner, R.; Lang, H.

Twin monomers [Mg(2-OCH2-cC6H4O)][L]0.8 (2, L=diglyme) and [Mg(2-OCH2-cC6H4O)][L]0.66 (3, L=tmeda) form by their thermal polymerization interpenetrating organic-inorganic hybrid materials in a straightforward manner. Carbonization (Ar) followed by calcination gave porous MgO (2: surface area 200 m2g-1, 3: 400 m2g-1), which showed in catalytic studies towards Meerwein-Ponndorf-Verley reductions excellent yields and complete conversions for cyclohexanone and benzaldehyde. However, with crotonaldehyde a mixture of C4–C8 compounds was obtained. When MgO was exposed to air then primarily crotyl alcohol was formed. The range of applications could be easily extended by twin polymerization of 3 in presence of [Cu-(O2CCH2O(CH2CH2O)2Me)2] (4) or [Ag(O2CCH2-cC4H3S)(PPh3)] (5), resulting in the formation of nanoparticle-decorated porous CuO@MgO or Ag@MgO materials, which showed high catalytic reactivity towards the reduction of methylene blue.

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