LAUSR

Three novel tetranuclear cobalt(II) complexes [Co4L2(μ1,1,1-N3)2(N3)2] (1), [Co4L2(μ3-OH)2(NCS)2]·4CH3CN (2) and [Co4L2(μ3-OH)2(NCSe)2]·2CH3CN (3) have been synthesized on reacting a Mannich base ligand, N,N′-dimethyl-N,N′-bis(2-hydroxy-3-methoxy-5-methylbenzyl)ethylenediamine (H2L), with cobalt(II) acetate tetrahydrate in the presence of azide, thiocyanate and selenocynate salts, respectively. Single crystal X-ray structural analyses showed that these discrete tetranuclear Co(II) complexes possess defect dicubane cores with μ1,1,1-N3 (for 1) and μ3-OH bridges (for 2 and 3). Magnetic susceptibility measurements showed prominent intramolecular ferromagnetic interactions for 1 (J1/kB = −19 K, J2/kB = 38 K) and dominant antiferromagnetic interactions for 2 and 3 (J1/kB = 4.7 K, J2/kB = −34 K for 2 and J1/kB = 4.4 K, J2/kB = −12 K for 3). All three complexes (1–3) exhibited phenoxazinone synthase-like catalytic activity towards the aerobic oxidation of o-aminophenol. The turn over numbers (Kcat) for the aerobic oxidation of o-aminophenol were calculated to be 500.4, 508.9 and 511.2 h−1 for complexes 1–3, respectively. The mechanism of phenoxazinone synthase-like catalytic activity has also been proposed for these tetranuclear Co(II) catalysts with the help of mass spectral analysis.