The background of the investigation is constituted by reactive moieties and intermediates playing relevant roles on the surfaces of vanadiumoxide-based catalysts during the oxygenation/dehydrogenation of organic substrates. With the aim of modeling such species, a series of mono- and dinuclear charged and uncharged vanadium oxo complexes containing p-tert-butylated calix[4] arene and calix[8] arene ligands (denoted H4B and H8B", respectively, in the protonated forms) has been synthesized and characterized: PPh4[O = VB] ((PPh4)1), O = VBOAc (2), PPh4[O2V2HB"] (3), and [mu-O(O=V(OMe))(2)B-Me2] (4), where superscripts OAc and Me2 indicate that one or two protons of H4B are substituted by these residues, respectively. These compounds were analyzed both in solution and by means of single-crystal X-ray crystallography; it turned out that the crystal structures are retained on dissolution (2 changed only from the paco to the cone structure). In the case of 4, it could be shown that the bulk product consists of a mixture of two isomers (4(t) and 4(c)) differing in the relative positions of the vanadium-bound methoxy groups. Subsequently, all compounds were tested as catalysts for the oxidation of alcohols with O-2. It turned out that the two dinuclear complexes efficiently catalyze the oxidation of 1-phenyl-1-propargyl alcohol and fluorenol; in addition, they even show some activity with respect to the oxidation of dihydroanthracene. This may hint to a higher activity of dinuclear sites on the surfaces of heterogeneous catalysts as well.