New copper(II) dimer with 3-(2-hydroxy-4-nitrophenylhydrazo)pentane-2,4-dione and its catalytic activity in cyclohexane and benzyl alcohol oxidations

3-(2-Hydroxy-4-nitrophenylhydrazo)pentane-2,4-dione (H2L, 1) was synthesized by azocoupling of diazonium salts of 2-hydroxy-4-nitroaniline with pentane-2,4-dione and shown to exist in the hydrazone tautomeric form in the free state and in its new dicopper(II) complex [Cu2(H2O)2(μ-L)2] (2) whose X-ray crystal structure was determined. Complex 2 acts as a catalyst, under mild conditions, for the peroxidative oxidation (with H2O2) of cyclohexane to cyclohexanol, cyclohexanone and cyclohexyl hydroperoxide, in MeCN/H2O, and for the aerobic TEMPO-mediated selective oxidation of benzylic alcohols to the corresponding aldehydes, thus showing that azoderivatives of β-diketones can be the suitable ligands for such types of reactions.

The copper(II) complex [Cu2(H2O)2(μ-L)2] (H2L = 3-(2-hydroxy-4-nitrophenylhydrazo)pentane-2,4-dione) is catalytically active in the peroxidative oxidation of cyclohexane and in the TEMPO-mediated aerobic oxidation of benzylic alcohols.Figure optionsDownload high-quality image (81 K)Download as PowerPoint slide