K3Mo2O5.6F3.4 and K3V2O3.3F5.7 - exploring transition metal cation valence and anion distribution in oxyfluorides.

Oxyfluorides come in many different structures and are highly adaptable in composition, not least because of their mixed-anionic nature. Slight changes, unless specifically looked for, can easily go unnoticed. In this paper, we present two oxyfluorides, K3Mo2O5.6F3.4 and K3V2O3.3F5.7, synthesized under high-pressure/high-temperature conditions, and demonstrate the importance of careful analysis of composition, oxidation state and O/F anion distribution for an accurate description of oxyfluorides. Their crystal structures were determined by single-crystal X-ray diffraction and the transition metal cation valences analyzed by X-ray photoelectron spectroscopy (XPS). The O/F anion ratio was calculated using the principle of charge neutrality and the local distribution within the crystallographic framework was studied using bond valence (BV) and charge distribution (CHARDI) calculations. Madelung Part of Lattice Energy (MAPLE) calculations and magnetic measurements provide insight into phase stability and corroborate the mixed-valent nature of the compounds.

Salt-flux growth of HoCuMg4 single crystals.

Polycrystalline samples of the magnesium-rich intermetallic compounds RECuMg4 (RE = Dy, Ho, Er, Tm) were synthesized by reaction of the elements in sealed tantalum ampoules heated in a high-frequency induction furnace. Phase purity of the RECuMg4 phases was ascertained by powder X-ray diffraction patterns. Well-shaped single crystals of HoCuMg4 could be grown in a NaCl/KCl salt flux and the crystal structure was refined from single crystal X-ray diffraction data: TbCuMg4 structure-type, space group Cmmm, a = 1361.4(2), b = 2039.3(4), c = 384.62(6) pm. The crystal structure of the RECuMg4 phases can be understood as a complex intergrowth variant of CsCl and AlB2 related slabs. The remarkable crystal chemical motif concerns the orthorhombically distorted bcc-like magnesium cubes with Mg-Mg distances ranging from 306 to 334 pm. At high temperatures DyCuMg4 and ErCuMg4 are Curie-Weiss paramagnets with paramagnetic Curie-Weiss temperatures of -15 K and -2 K for RE = Dy and Er, respectively. The effective magnetic moments, 10.66µB for RE = Dy and 9.65µB for RE = Er prove stable trivalent ground states for the rare earth cations. Magnetic susceptibility and heat capacity measurements reveal long-range antiferromagnetic ordering at low temperatures (<21 K). Whereas DyCuMg4 exhibits two subsequent antiferromagnetic transitions at TN = 21 and 7.9 K which successively remove half of the entropy of a doublet crystal field ground state of Dy, ErCuMg4 shows a single, possibly broadened, antiferromagnetic transition at 8.6 K. The successive antiferromagnetic transitions are discussed with respect to magnetic frustration in the tetrameric units present in the crystal structure.

Experimental and computational study of the exchange interaction between the V(III) centers in the vanadium-cyclal dimer.

[V2(HCyclal)2] is prepared by controlled oxidation of vanadium nanoparticles at 50 °C in toluene. The V(0) nanoparticles are synthesized in THF by reduction of VCl3 with lithium naphthalenide. They exhibit very small particle sizes of 1.2 ± 0.2 nm and a high reactivity (e.g. with air or water). By reaction of V(0) nanoparticles with the azacrown ether H4Cyclal, [V2(HCyclal)2] is obtained with deep green crystals and high yield. The title compound exhibits a V(III) dimer (V⋯V: 304.1(1) pm) with two deprotonated [HCyclal]3- ligands as anions. V(0) nanoparticles as well as the sole coordination of V(III) by a crown ether as the ligand and nitrogen as sole coordinating atom are shown for the first time. Magnetic measurements and computational results point to antiferromagnetic coupling within the V(III) couple, establishing an antiferromagnetic spin S = 1 dimer with the magnetic susceptibility determined by the thermal population of the total spin ranging from ST = 0 to ST = 2.

bcc superstructures: RE2RuIn with RE = Sc, Y, Dy-Tm and Lu.

The rare earth-rich intermetallic phases RE2RuIn with RE = Sc, Y, Dy-Tm and Lu were synthesized by reactions of the elements in sealed tantalum ampoules in an induction furnace. The samples were characterized through Guinier powder patterns and the structures of Sc2RuIn and Er2RuIn were refined from single crystal X-ray diffraction data. The indides crystallize with the Pt2ZnCd type space group P4/mmm. The RE2RuIn phases are superstructures of the bcc packing and can be explained as intergrowth variants of tetragonally distorted, CsCl derived slabs of compositions RERu and REIn. Chemical bonding is discussed for Sc2RuIn and Sc2RuMg in comparison with the binaries ScRu, ScMg and ScIn. The Ru/Mg respectively Ru/In ordering leads to an increase of Sc-Sc bonding for the slab with the shorter Sc-Sc distances, while the Sc-Ru bond strength values remain similar. The strongest bonding interactions occur within the magnesium and indium square nets. Magnetic susceptibility measurements reveal Pauli paramagnetism for Lu2RuIn while Dy2RuIn, Ho2RuIn, Er2RuIn and Tm2RuIn are Curie-Weiss paramagnets. Antiferromagnetic ordering occurs at 13.1, 5.3 and 2.9 K for Dy2RuIn, Er2RuIn and Tm2RuIn, respectively. Dy2RuIn and Er2RuIn show metamagnetic transitions at critical fields of 4.6 and 3.2 T.