Two sterically hindered tris-pyridyl methane ligands, tris(6-methyl-2-pyridyl)methane (L1) and bis(6-methyl-2-pyridyl)pyridylmethane (L2), are newly synthesized. Under aerobic conditions, Ln (n 1 or 2) reacts with CuX2 (X = Cl or Br), oxygenated at the methine position to LnOH or LnOMe. The former alcoholate ligand creates trinuclear Cu(II) complexes [Cu-3(X)(LnO)(3)](PF6)(2) {(X, n) = (Br, 1) 1, (Cl, 1) 2, (Br, 2) 3, or (Cl, 2) 4} in which the alkoxide oxygen atoms bridge copper centers. The crystal structures of 1-4 are presented along with their magnetic susceptibility data. The weak antiferromagnetic coupling between the Cu(II) centers in this trinuclear arrangement is due to weak interaction of the magnetic orbitals (dz(2)) which are oriented along three alternate sides in a hexagon of the Cu3O3 core in 1-4. Under anaerobic conditions, L1 reacts with CuBr2 to form a square pyramidal complex [CuL1Br(2)] (9) with the ligand facially capping. [Cu(Br)(2)(L1OMe)] (10) was obtained after the suspension of 9 in MeOH was stirred under air for 48 h. In the presence of cyclohexene, 9 is converted to [Cu(Br)(L1)](m) (m = 1 or 2) 5 quantitatively to give trans-1,2-dibromocyclohexane, indicating that Br-2 is generated during the reaction. The FAB MS spectrum of [O-18]-1 prepared by the reaction of L1 with CuBr2 under O-18(2) shows that the ligand of [O-18]-1 is L1(18)O(-). L1(18)OH, L1OCD(3), and bis(6-methyl-2-pyridyl) ketone were obtained from reaction of L1 with CuBr2 in CD3OD under O-18(2). These results indicate that the origins of the O atom in L1OH and L1OMe are O-2 and MeOH, respectively. On the basis of these results, a mechanism of the oxygenation of L1 in the present system will be proposed.