Tuning spin dynamics of binuclear Dy complexes using different nitroxide biradical derivatives.

By employing nitronyl/imino nitroxide biradicals, three Ln-Zn complexes, namely, [Ln 2 Zn 2 (hfac) 10 (ImPhPyobis) 2 ] (Ln III = Gd 1, Dy 2; hfac = hexafluoroacetylacetonate; ImPhPyobis = 5-(4-oxypyridinium-1-yl)-1,3-bis(1'-oxyl-4',4',5',5'-tetramethyl-4,5-hydro-1 H -imidazol-2-yl)benzene) and [Dy 2 Zn 2 (hfac) 10 (NITPhPyobis) 2 ] 3 (NITPhPyobis = 5-(4-oxypyridinium-1-yl)-1,3-bis(1'-oxyl-3'-oxido-4',4',5',5'-tetramethyl-4,5-hydro-1 H -imidazol-2-yl)benzene), have been successfully prepared. The three complexes possess {Ln 2 O 2 } cores bridged by the oxygen atoms of the 4-oxypyridinium rings of the biradical ligands and one of the imino/nitronyl nitroxide groups of the biradical is coordinated to a Zn II ion, then producing a centrosymmetric tetranuclear six-spin structure. The studies of spin dynamics indicate that complexes 2 and 3 exhibit distinct magnetic relaxation behaviors at zero dc field: complex 2 presents single relaxation with an effective energy barrier ( U eff ) of 69.8 K, while complex 3 exhibits double relaxation processes with U eff values for the fast and slow relaxation being 15.8 K and 50.9 K, respectively. The observed different magnetic relaxation behaviors for the two Dy complexes could be mainly ascribed to the influence of the distinct nitroxide biradical derivatives.