An environmentally friendly protocol is described for an economic, practical laboratory-scale oxidation
of primary and secondary alcohols to aldehydes and ketones, using a bis-chloro-bridged binuclear Cu(II)
complex [(HL)Cu(μ2-Cl)2Cu(HL)]*1.5 CH3OH as catalyst. The catalyst was prepared in situ from commercially
available reagents and is characterized by single crystal X-ray analysis, FT-IR, UV-visible spectra, mass
spectrometry, and powder x-ray diffraction (PXRD). The geometry of the complex has been optimized using
the B3LYP level of theory confirming the experimental data. Our results demonstrated well the efficiency,
selectivity and stability of this new catalyst in the oxidation of alcohols in ethanol and tert-butyl hydroperoxide
(tBuOOH) as a green solvent and oxidant, respectively. Turnover number and reusability have proven the high
efficiency and relative stability of the catalyst.