We report a series of 3d-4f complexes {Ln2 Cu3 (H3 L)2 Xn } (X=OAc(-) , Ln=Gd, Tb or X=NO3 (-) , Ln=Gd, Tb, Dy, Ho, Er) using the 2,2'-(propane-1,3-diyldiimino)bis[2-(hydroxylmethyl)propane-1,3-diol] (H6 L) pro-ligand. All complexes, except that in which Ln=Gd, show slow magnetic relaxation in zero applied dc field. A remarkable improvement of the energy barrier to reorientation of the magnetisation in the {Tb2 Cu3 (H3 L)2 Xn } complexes is seen by changing the auxiliary ligands (X=OAc(-) for NO3 (-) ). This leads to the largest reported relaxation barrier in zero applied dc field for a Tb/Cu-based single-molecule magnet. Ab initio CASSCF calculations performed on mononuclear Tb(III) models are employed to understand the increase in energy barrier and the calculations suggest that the difference stems from a change in the Tb(III) coordination environment (C4v versus Cs ).
Keywords: copper; heterometallic complexes; lanthanides; magnetic properties; single-molecule magnets.
© 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.