Field-induced slow magnetic relaxation in mixed valence di- and tri-nuclear Co^II-Co^III complexes

Two novel mixed valence Co^II-Co^III complexes, namely [Co^IICo^III(L1)(ab)(mb)₂(H₂O)]·dmf (1) and [CoCo^II(L2)₄(H₂O)₄]·2H₂O (2) [H₂L1 = (E)-2-((1-hydroxybutan-2-ylimino)methyl)-6-methoxyphenol, ab = 2-amino-butan-1-ol anion, mb = p-methyl benzoate, H₂L2 = 3-((2-hydroxy-3-methoxy-benzylidene)-amino)-propionic acid, and dmf = N,N-dimethyl-formamide], were synthesized and characterized by single crystal X-ray diffraction and magnetic studies at low temperature. The structure determination reveals that both complexes belong to the monoclinic system with P21/c (1) and I2/a (2) space groups. Complex 1 is a dinuclear Co^IIICo^II compound with distorted octahedral cobalt centers showing different coordination environments. In 2, a bent trinuclear CoCo^II complex, the coordination environments around the two terminal Co^III sites are alike, whereas they are different in the central Co^II ion. Alternating current/direct current (ac/dc) magnetic studies revealed that both complexes show field-induced slow magnetic relaxation. The dc magnetic susceptibility and magnetization data were analyzed with the following Hamiltonianwhere D and E are the axial and rhombic zero-field splitting (zfs) parameters, respectively, and a good agreement between experimental and simulated results was found using the parameters g_⊥ = 2.585, g_∥ = 2.437, D = +98.1 cm^-1, E/D = 0.008 and F = 8.2× 10^-5 for 1 and g_⊥ = 2.580, g_∥ = 2.580, D = +55.4 cm^-1, and E/D = 0.000 for 2.