| Abstrakt: |
The first use of the organic chelate N-hydroxy-1,8-naphthalimide (hynadH) in DyIII chemistry has unveiled access to a synthetic 'playground' composed of four new dinuclear complexes, all of which possess the same planar {Dy2(µ-OR)2}4+ diamond-shaped core, resulting from the bridging and chelating capacity of the hynad-groups. The structural stability of the central {Dy2} core has allowed for the modulation of the peripheral coordination sites of the metal ions, and specifically the NO3 -/hynad-ratio of capping groups, thus affording the compounds [Dy2(hynad)2(NO3)4(DMF)2] (1), (Me4N)2[Dy2(hynad)2(NO3)6] (2), [Dy2(hynad)4(NO3)2(H2O)2] (3), and [Dy2(hynad)6(H2O)2] (4). Because of the chemical and structural modifications in the series 1-4, the DyIII coordination polyhedra are also dissimilar, comprising the muffin (1 and 3), tetradecahedral (2), and spherical tricapped trigonal prismatic (4) geometries. Complexes 1, 2, and 4 exhibit a ferromagnetic response at low temperatures, while 3 is antiferromagnetically coupled. All compounds exhibit out-of-phase (?''M) ac signals as a function of ac frequency and temperature, thus behaving as single-molecule magnets (SMMs), in the absence or presence of applied dc fields. Interestingly, the hynad--rich and nitrato-free complex 4, demonstrates the largest energy barrier (Ueff = 69.62(1) K) for the magnetization reversal which is attributed to the presence of the two axial triangular faces of the spherical tricapped trigonal prism by the negatively charged O-atoms of the hynad-ligands. [ABSTRACT FROM AUTHOR] |
