Hydrothermal synthesis of lanthanide rhenium oxides: Structures and magnetism of Ln2Re2O7(OH) (Ln = Pr, Nd) and Ln4Re2O11 (Ln = Eu, Tb)

Abstract

Abstract The reactions of Ln2O3 (Ln\u202f=\u202fLa Lu) with ReO2 were examined in high temperature hydrothermal water (650\u202f°C). In all cases the rhenium oxide was added in a three-fold excess. No external mineralizer was needed and the rhenate itself acted as a sufficient mineralizer to form high quality single crystals of several crystalline products. These form in good yield with compositions varying as a function of the size of the rare earth ion. The largest sesquioxide, La2O3, forms the well-known La4Re6O19 phase, but when Ln\u202f=\u202fNd or Pr, a new product, Ln2Re2O7(OH), is isolated. Reactions with Ln\u202f=\u202fSm Tb form Ln4Re2O11, and those with Dy Lu form Ln2ReO5. The new Ln2Re2O7(OH) series was characterized as a new structure type by single crystal X-ray diffraction. This structure features a tetrameric Re4O16 cluster embedded in a lanthanide oxide framework. Additional detailed structural data is also provided for Tb4Re2O11 and Eu4Re2O11, which were not previously reported for the Ln4Re2O11 family. In Ln2Re2O7(OH), no direct Re Re bond (Re Re\u202f=\u202f2.60\u202fA) is observed while Ln4Re2O11 appears to possess a rhenium-rhenium double bond with a Re Re distance of 2.42\u202fA. Single crystal Raman data supports both of these characterizations. Magnetic data is reported for Ln2Re2O7(OH) and Tb4Re2O11, and their behavior appears to be dominated by the f-element magnetic moments. At low temperatures Tb4Re2O11 displays possible canted antiferromagnetic coupling.