Abstract
Two μ-phenoxo-μ1,1-azide dinuclear CoIIICoII complexes [CoIII(N3)2L1(μ1,1-N3)CoII(N3)]·MeOH (1) and [CoIII(N3)2L2(μ1,1-N3)CoII(N3)]·MeOH (2) (HL1 and HL2 are two Schiff base ligands having N2O-N2O compartments) both possess one hexacoordinate Co(iii) and one pentacoordinate Co(ii) center. DC magnetic susceptibility and magnetization measurements show an appreciable amount of positive magnetic anisotropy (D/hc∼ 40 cm-1) that is also confirmed by ab initio CASSCF calculations. AC susceptibility measurements of 1 reveal that it exhibits a slow magnetic relaxation with two relaxation channels. The external magnetic field supports the low-frequency (LF) channel that escapes on heating more progressively than the high-frequency (HF) branch. The relaxation time is as slow as τ = 255 ms at T = 1.9 K and BDC = 0.6 T, where the LF mole fraction is 69%. The complex 2 also displays similar field-supported slow magnetic relaxation with two relaxation channels.
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