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7840402 
Journal Article 
Cyclohexane oxidation continues to be a challenge 
Schuchardt, U; Cardoso, D; Sercheli, R; Pereira, R; de Cruz, RS; Guerreiro, MC; Mandelli, D; Spinace, EV; Fires, EL 
2001 
1 
Applied Catalysis A: General
ISSN: 0926-860X
EISSN: 1873-3875 
211 
1 
1-17 
English 
WOS:000167626600001 
Many efforts have been made to develop new catalysts to oxidize cyclohexane under mild conditions. Herein, we review the most interesting systems for this process with different oxidants such as hydrogen peroxide, tert-butyl hydroperoxide and molecular oxygen. Using H2O2, Na-GeX has been shown to be a most stable and active catalyst. Mesoporous TS-1 and Ti-MCM-41 are also stable, but the use of other metals such as Cr, V, Fe and Mo leads to leaching of the metal. Homogeneous systems based on binuclear manganese(IV) complexes have also been shown to be interesting. When t-BuOOH is used, the active systems are those phthalocyanines based on Ru, Co and Cu and polyoxometalates of dinuclear ruthenium and palladium. Microporous metallosilicates containing different transition metals showed leaching of the metal during the reactions. Molecular oxygen can be used directly as an oxidant and decreases the leaching of active species in comparison to hydrogen peroxide and tert-butyl hydroperoxide. Metal aluminophosphates (metal: Mn, Fe, Co, Cu, Cr V) are active and relatively stable under such conditions. Mn-AlPO-36 yields directly adipic acid, but large amounts of carboxylic acids should be avoided, as they cause metal leaching from the catalysts. Rare earth exchanged zeolite Y also shows good selectivity and activity. In the last part of the review, novel alternative strategies for the production of cyclohexanol and cyclohexanone and the direct synthesis of adipic acid are discussed. 
cyclohexane oxidation; cyclohexanone; adipic acid; hydrogen peroxide; tert-butyl hydroperoxide; molecular oxygen