Osmium borides
Osmium borides are compounds of osmium and boron. Their most remarkable property is potentially high hardness. It is thought that a combination of high electron density of osmium with the strength of boron-osmium covalent bonds will make osmium borides superhard materials, however this has not been demonstrated yet. For example, OsB2 is hard (hardness comparable to that of sapphire), but not superhard.[1]
Synthesis
[edit]Osmium borides are produced in vacuum or inert atmosphere to prevent formation of osmium tetroxide, which is a hazardous compound. Synthesis occurs at high temperatures (~1000 °C) from a mixture of MgB2 and OsCl3.[1]
Structure
[edit]Three osmium borides are known: OsB, Os2B3 and OsB2. The first two have hexagonal structure,[2] similar to that of rhenium diboride. Osmium diboride was first also sought as hexagonal,[3] but one of its phases was later reassigned to orthorhombic.[1][4] In recent methods of synthesis, it has also been found that a hexagonal phase of OsB2 exists with a similar structure to ReB2.[5]
References
[edit]- ^ a b c Cumberland, Robert W.; et al. (April 27, 2005). "Osmium Diboride, An Ultra-Incompressible, Hard Material". Journal of the American Chemical Society. 127 (20): 7264–5. doi:10.1021/ja043806y. PMID 15898746.
- ^ M. Hebbache; et al. (2006). "A new superhard material: Osmium diboride OsB2". Solid State Communications. 139 (5): 227–231. Bibcode:2006SSCom.139..227H. doi:10.1016/j.ssc.2006.05.041.
- ^ Kempter, C. P.; Fries, R. J. (1961). "Crystallography of the Ru-B and Os-B Systems". The Journal of Chemical Physics. 34 (6): 1994. Bibcode:1961JChPh..34.1994K. doi:10.1063/1.1731807.
- ^ Roof, R. B.; Kempter, C. P. (1962). "New Orthorhombic Phase in the Ru-B and Os-B Systems". The Journal of Chemical Physics. 37 (7): 1473. Bibcode:1962JChPh..37.1473R. doi:10.1063/1.1733309. OSTI 4787761.
- ^ Xie, Zhilin; Blair, Richard G.; Orlovskaya, Nina; Cullen, David A.; Andrew Payzant, E. (2014-11-01). "Thermal stability of hexagonal OsB2". Journal of Solid State Chemistry. 219: 210–219. Bibcode:2014JSSCh.219..210X. doi:10.1016/j.jssc.2014.07.035.