Two new dysprosium(III) complexes, [Dy2(HL1)4(CO3)]·4H2O (1) and [Dy2(L2)2(NO3)2(CH3OH)2]·4CH3CN (2), have been synthesized from the Schiff-base ligands N′-((2-hydroxy-1-naphthyl)methylene)benzohydrazide (H2L1) and N′-((2-hydroxy-1-naphthyl)methylene) picolinohydrazide (H2L2). Single-crystal X-ray diffraction studies reveal that four mono-deprotonated H2L1 ligands and two di-deprotonated H2L2 ligands which have undergone keto–enol tautomerism coordinate to the two dysprosium centres of complexes 1 and 2, respectively. The dc magnetic properties of complexes 1 and 2 are different. The phenoxido bridges in complex 1 mediate antiferromagnetic interaction between DyIII ions, while ferromagnetic interaction was clearly observed in alkoxido-bridged dinuclear complex 2. Furthermore, both complexes show frequency-dependent ac magnetic susceptibilities, indicating a slow relaxation of the magnetization, typical of SMM behaviour.
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