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Autoxidation Chemistry: Bridging the Gap Between Homogeneous Radical Chemistry and (Heterogeneous) Catalysis
Authors:Ive Hermans  Jozef Peeters  Pierre A. Jacobs
Affiliation:1. Department of Microbial and Molecular Systems (M2S), Centre for Surface Chemistry and Catalysis, K. U. Leuven, Kasteelpark Arenberg 23, 3001, Leuven, Belgium
2. Institute for Chemical and Bioengineering, ETH Zürich, H?nggerberg, HCI, Wolfgang-Pauli-Str. 10, 8093, Zurich, Switzerland
3. Department of Chemistry, K. U. Leuven, Celestijnenlaan 200F, 3001, Leuven, Belgium
Abstract:During the autoxidation of cyclohexane, abstraction of the αH-atom of the hydroperoxide product by chain-carrying peroxyl radicals produces both the desired alcohol and ketone products, as well as the majority of by-products. Rationalizing the impact of this reaction, one should aim for a (catalytic) destruction of this hydroperoxide without the intervention of peroxyl chain-carriers. Starting from these new insights in the molecular mechanism, attempts for rational catalyst design are initiated.
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