Strategy for the rational design of asymmetric triply bridged dinuclear 3d-4f single-molecule magnets |
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Authors: | Colacio Enrique Ruiz-Sanchez José White Fraser J Brechin Euan K |
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Institution: | Departamento de Qui?mica Inorga?nica, Facultad de Ciencias, Universidad de Granada, Av. Fuentenueva S/N, 18071 Granada, Spain. ecolacio@ugr.es |
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Abstract: | Three triply bridged M(II)-Dy(III) dinuclear complexes, Ni(μ-L)(μ-OAc)Dy(NO(3))(2)] 1, Zn(μ-L)(μ-OAc)Dy(NO(3))(2)] 2, and Ni(μ-L)(μ-NO(3))Dy(NO(3))(2)]·2CH(3)OH 3 were prepared with a new and flexible compartmental ligand, N,N',N″-trimethyl-N,N″-bis(2-hydroxy-3-methoxy-5-methylbenzyl)diethylene triamine (H(2)L), containing N(3)O(2)-inner and O(4)-outer coordination sites. These complexes have diphenoxo/acetate (1 and 2) or diphenoxo/nitrate (3) asymmetric bridging fragments. Compounds 1 and 3 exhibit ferromagnetic interaction between Ni(2+) and Dy(3+) ions and frequency dependence of the out-of-phase (χ″(M)) alternating current (ac) susceptibility signal characteristic of single-molecule-magnet behavior. The energy barriers Δ/k(B) for compound 3 under zero and 1000 Oe applied direct current (dc) magnetic fields were estimated from the Arrhenius plots to be 7.6 and 19.1 K, respectively. |
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