Abstract

A theoretical model is developed for the explanation of the magnetic properties of the [MnCl] 4[Re(triphos)(CN) 3] 4 single molecule magnet, which represents a 3d–5d molecular cube compressed along one of the C 3 axes. In the model, the strong local trigonal crystal field on each Re(II) ion is assumed to split the ground cubic 2 T 2( t 2 5 ) term into the states 2 A 1 and 2 E in such a way that 2 E term proves to be the ground one. The ground Kramers doublet that appears under the spin–orbit splitting of the 2 E term is shown to be fully anisotropic ( g ⊥ = 0) and the magnetic superexchange (mediated by cyanide bridge) between Re and Mn ions is approximated by the Ising-like Hamiltonian. In this case, the magnetic anisotropy of the trigonally distorted cube represents a first order effect that is totally incorporated in the effective Ising-like Hamiltonian, including the pseudo-spin-1/2 operator for the Re(II) ion and the operator of the true spin-5/2 for the Mn(II) ion. The developed pseudo-spin-1/2 formalism is applied to the explanation of the DC magnetic susceptibility and magnetization data, and the set of the best fit parameters is found. The temperature dependence of the DC magnetic susceptibility and the field dependence of the magnetization calculated with this set of parameters are in accord with the experimental data being at the same time compatible with the existence of the barrier for magnetization reversal. Finally, the applicability of the quantum–classical spin approach for the calculation of the magnetic properties of large 3d–5d clusters is discussed.

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