文摘
In this report, we present combined experimental and theoretical studies of the trinuclear {[L<sub>2sub>Co<sub>2sub>Tb][NO<sub>3sub>]} (LH<sub>3sub> = (S)P[N(Me)N鈺怌H鈥擟<sub>6sub>H<sub>3sub>-2-OH-3-OMe]<sub>3sub>) complex exhibiting single molecule magnet properties. Our theoretical model includes the axial crystal fields acting on the Tb<sup>IIIsup> and Co<sup>IIsup> ions, the spin鈥搊rbit interaction operating within the <sup>4sup>T<sub>1sub> ground term of the Co<sup>IIsup> ion, and the ferromagnetic exchange between Tb and Co magnetic centers. We demonstrate for the [L<sub>2sub>Co<sub>2sub>Tb]<sup>+sup> complex that the strong negative single-ion anisotropy of both Tb<sup>IIIsup> and Co<sup>IIsup> ions is the reason for the observed slow relaxation of magnetization. The elaborated model describes perfectly the experimental magnetic properties of the complex as a function of temperature and the external magnetic field.