Ti2Rh6B – a new boride with a double perovskite-like structure containing octahedral Rh6 clusters
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Boniface P. T. Fokwa
, Bernhard Eck and Richard Dronskowski
Abstract
Single crystals of Ti2Rh6B were synthesized by arc-melting the elements in a water-cooled copper crucible under an argon atmosphere. The new silver-like compound with metallic luster crystallizes in space group Fm-3m (no. 225) with a = 7.8191(5) Å, V = 478.05(5) Å3, and Z = 4. The refinement converged to R1 = 0.0169 and wR2 = 0.0486 for all 96 unique reflections and 7 parameters. The structure can be described as a defect double perovskite, A2BB'O6, where the A site is occupied by titanium, the B site by boron, the O site by rhodium but the B' site is vacant leading to the formation of perfectly octahedral Rh6 clusters and BRh6 units. Rh—B, Rh—Ti, and Rh—Rh interactions are observed. According to density-functional (LMTO) electronic structure calculations, the strongest bonding occurs for the Rh—B contacts, and the Rh—Rh bonding within the clusters is more than two times stronger than in the BRh6 units.
© by Oldenbourg Wissenschaftsverlag, München
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Articles in the same Issue
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- Fritz H. Laves – 100 years young
- Fritz H. Laves – an ideal for generations
- Gustav E. R. Schulze's pioneering work on Laves phases
- Preparation, phase stability and structure of the C36 Laves phase Nb1–xCo2+x
- Atom order and thermodynamic properties of the ternary Laves phase Ti(TiyNixAl1–x–y)2
- Atomic ordering in the Laves phases L1 V(Co1–xSix)2 (x = 0.43 and 0.56)
- Microscopic structures of Laves phases and structurally related compounds: a transmission electron microscopy study
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- High-pressure crystal chemistry of binary intermetallic compounds
- Re3B type intermetallics — crystal chemistry, bonding and properties
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- On the formation and crystal structure of the Pd6B phase
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