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Chemistry. 2016 Aug 22;22(35):12307-11. doi: 10.1002/chem.201602964. Epub 2016 Jul 27.

Cooperative Catalysis for Selective Alcohol Oxidation with Molecular Oxygen.

Chemistry (Weinheim an der Bergstrasse, Germany)

Thierry K Slot, David Eisenberg, Dylan van Noordenne, Peter Jungbacker, Gadi Rothenberg

Affiliations

  1. Van 't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, 1098 XH, Amsterdam, The Netherlands.
  2. Van 't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, 1098 XH, Amsterdam, The Netherlands. [email protected].
  3. Van 't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, 1098 XH, Amsterdam, The Netherlands. [email protected].

PMID: 27355443 DOI: 10.1002/chem.201602964

Abstract

The activation of dioxygen for selective oxidation of organic molecules is a major catalytic challenge. Inspired by the activity of nitrogen-doped carbons in electrocatalytic oxygen reduction, we combined such a carbon with metal-oxide catalysts to yield cooperative catalysts. These simple materials boost the catalytic oxidation of several alcohols, using molecular oxygen at atmospheric pressure and low temperature (80 °C). Cobalt and copper oxide demonstrate the highest activities. The high activity and selectivity of these catalysts arises from the cooperative action of their components, as proven by various control experiments and spectroscopic techniques. We propose that the reaction should not be viewed as occurring at an 'active site', but rather at an 'active doughnut'-the volume surrounding the base of a carbon-supported metal-oxide particle.

© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Keywords: active sites; cooperative effects; heterogeneous catalysts; oxygen; supported catalysts

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