Abstract
Abstract The reaction of [MnII(S-mandelato)2] complexes with 5-Methyl-salicylaldoxim (5-Me-saloxH2) leads to the chiral hexanuclear manganese(III) complex [Mn6(μ3-O)2(5-Me-salox)6(S-mandelato)2(EtOH)6]. The structure can be viewed as two neutral stacked {Mn3(μ3-O)(5-Me-salox)3(S-mandelato)(EtOH)3} triangular subunits linked together in a head-to-tail manner by two phenoxo and two oximato μ3-oxygen atoms of the deprotonated oxime groups of the ligands. The magnetic study of this chiral hexanuclear manganese(III) complex reveals a SMM behaviour with an energy barrier of the slow relaxation of the magnetisation equal to 35 K. Considering the structural features, the fitting of the temperature dependence of the magnetic susceptibility gives a good agreement with the experimental data considering two sets of interactions: J1 = +0.37 cm−1 and J2 = −0.70 cm−1 within (ferromagnetic) and between (antiferromagnetic), respectively, the {Mn3(μ3-O)(5-Me-salox)3(S-mandelato)(EtOH)3} triangular subunits.
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