Field-Induced Slow Magnetic Relaxation of GdIII Complex with a Pt-Gd Heterometallic Bond.
Takefumi YoshidaGoulven CosquerDavid Chukwuma IzuoguHiroyoshi OhtsuMasaki KawanoYanhua LanWolfgang WernsdorferHiroyuki NojiriBrian K BreedloveMasahiro YamashitaPublished in: Chemistry (Weinheim an der Bergstrasse, Germany) (2017)
Heterometallic Gd-Pt complexes ([Gd2 Pt3 (H2 O)2 (SAc)12 ] (SAc=thioacetate), [Y1.4 Gd0.6 Pt3 (H2 O)2 (SAc)12 ], and [Gd2 Pt3 (H2 O)6 (SAc)12 ]⋅7 H2 O have been synthesized. The crystal structures and DFT calculations indicated a Gd-Pt heretometallic bond. Single-crystal ESR spectra determined the direction of magnetic anisotropy as direction of the Gd-Pt bond. In other words, the Gd-Pt bond dictates the direction of magnetic anisotropy. The heterometallic Gd-Pt bond lowers the symmetry of the Gd ion, splitting the Kramers doublet in a dc field. Thus, we observed clear field-induced slow magnetic relaxation of [Y1.4 Gd0.6 Pt3 (H2 O)2 (SAc)12 ] up to 36 K. The relaxation process was determined to be a direct process.