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Heterometallic [Mn5-Ln4] single-molecule magnets with high anisotropy barriers
Authors:Mereacre Valeriu  Ako Ayuk M  Clérac Rodolphe  Wernsdorfer Wolfgang  Hewitt Ian J  Anson Christopher E  Powell Annie K
Affiliation:1. Institut für Anorganische Chemie der Universit?t Karlsruhe, Engesserstr. Geb. 30.45, 76128 Karlsruhe, Germany, Fax: (+49)?721‐608‐8142;2. Université Bordeaux 1, CNRS, Centre de Recherche Paul Pascal–UPR8641, 115 av. du Dr. Albert Schweitzer, 33600 Pessac, France, Fax: (+33)?556‐84‐56‐00;3. Institut Néel CNRS, BP 166, 25 av. des Martyrs, 38042 Grenoble, France
Abstract:The reaction of [Mn6O2(Piv)(10)(4-Me-py)(2.5)(PivH)(1.5)] (1) (py: pyridine, Piv: pivilate) with N-methyldiethanolamine (mdeaH2) and Ln(NO3)3 x 6 H2O in MeCN leads to a series of nonanuclear compounds [Mn5Ln4(O)6(mdea)2(mdeaH)2(Piv)6(NO3)4(H2O)2]2 MeCN (Ln=Tb(III) (2), Dy(III) (3), Ho(III) (4), Y(III) (5)). Single-crystal X-ray diffraction shows that compounds 2-5 are isostructural, with the central core composed of two distorted {Mn(IV)Mn(III)Ln2O4} cubanes sharing a Mn(IV) vertex, representing a new heterometallic 3d-4f motif for this class of ligand. The four new compounds display single-molecule magnet (SMM) behaviour, which is modulated by the lanthanide ion used. Moreover, the values found for Delta(eff) and tau(o) for 3 of 38.6 K and 3.0 x 10(-9) s respectively reveal that the complex 3 exhibits the highest energy barrier recorded so far for 3d-4f SMMs. The slow relaxation of the magnetisation for 3 was confirmed by mu-SQUID measurements on an oriented single crystal and the observation of M versus H hysteresis loops below 1.9 K.
Keywords:cluster compounds  lanthanides  magnetic properties  manganese  single‐molecule magnets
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