Increasing the Ketone Selectivity of the Cobalt-Catalyzed Radical Chain Oxidation of Cyclohexane

• Published in: Chemistry : a European journal 2002-08, Vol.8 (16), p.3724-3731
• Main Authors: Nowotny, Mathias, Pedersen, Lone N., Hanefeld, Ulf, Maschmeyer, Thomas
• Format: Article
• Language: English
• Subjects: carboxylate ligands; cobalt; heterogeneous catalysis; immobilization; mesoporous materials; oxidation
• ISSN: 0947-6539; 1521-3765
• DOI: 10.1002/1521-3765(20020816)8:16<3724::AID-CHEM3724>3.0.CO;2-W

A variety of heterogeneous catalysts for the radical chain oxidation of cyclohexane has been prepared by immobilization of the well‐defined cobalt acetate oligomers [py3Co3(μ3‐O)(OH)(O2CCH3)5](PF6) (1) and [py4Co2(OH)2(O2CCH3)3](PF6) (2) on carboxy‐modified mesoporous silica supports A–D by carboxylate exchange. The catalytic oxidation of cyclohexane with tert‐butyl hydroperoxide (TBHP) in the presence of these homogeneous and immobilized cobalt acetate complexes afforded the corresponding alcohol and ketone in high yield. The immobilization of 1 and 2 results in a significant increase of catalytic activity. TBHP acts as a radical initiator and as source of molecular oxygen, which is also involved in the overall oxidation process. The rate of cyclohexane conversion is limited by the diffusion of molecular oxygen, and steady‐state concentrations of cyclohexanone (K, ketone) and cyclohexanol (A, alcohol) are established; these determine the maximum K:A ratio. Highly active and stable catalysts for the oxidation of cyclohexane have been prepared by immobilization of cobalt acetate oligomers [py3Co3(μ3‐O)(OH)(O2CCH3)5](PF6) and [py4Co2(OH)2(O2CCH3)3](PF6) on various carboxy‐modified mesoporous silica supports (see scheme). The oxidation of cyclohexane by tert‐butyl hydroperoxide (TBHP) in the presence of these catalysts affords the corresponding alcohol and ketone with high selectivity. The course of the catalytic reaction has been studied in detail.