Jump to content

Potassium osmate

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Citation bot (talk | contribs) at 02:03, 23 September 2023 (Alter: template type. Add: chapter, series, publisher. Removed parameters. Some additions/deletions were parameter name changes. | Use this bot. Report bugs. | Suggested by Whoop whoop pull up | Category:Osmium compounds | #UCB_Category 17/23). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Potassium osmate
Names
Other names
Potassium osmate(VI) dihydrate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.157.189 Edit this at Wikidata
EC Number
  • 243-247-1
UNII
  • InChI=1S/2K.4H2O.2O.Os/h;;4*1H2;;;/q2*+1;;;;;2*-1;+4/p-4
    Key: DDTIHYGDUUGVNU-UHFFFAOYSA-J
  • [K+].[K+].[O-][Os](O)(O)(O)(O)[O-]
Properties
H4K2O6Os
Molar mass 368.42
Appearance purple solid
Hazards
GHS labelling:
GHS06: Toxic
Danger
H301, H311, H330, H331
P260, P261, P264, P270, P271, P280, P284, P301+P310, P302+P352, P304+P340, P310, P311, P312, P320, P321, P322, P330, P361, P363, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Potassium osmate is the inorganic compound with the formula K2[OsO2(OH)4]. This diamagnetic purple salt contains osmium in the VI (6+) oxidation state.[1] When dissolved in water a pink solution is formed but when dissolved in methanol, the salt gives a blue solution.[1] The salt gained attention as a catalyst for the asymmetric dihydroxylation of olefins.[2]

Structure

The complex anion is octahedral. Like related d2 dioxo complexes, the oxo ligands are trans.[3] The Os=O and Os-OH distances are 1.75(2) and 1.99(2) Å, respectively. It is a relatively rare example of a metal oxo complex that obeys the 18e rule.

Preparation

The compound was first reported by Edmond Frémy in 1844.[4] Potassium osmate is prepared by reducing osmium tetroxide with ethanol:[5]

2 OsO4 + C2H5OH + 5 KOH → CH3CO2K + 2 K2[OsO2(OH)4]

Alkaline oxidative fusion of osmium metal also affords this salt.[1]

See also

References

  1. ^ a b c F. Albert Cotton; Geoffrey Wilkinson (1966). Advanced Inorganic Chemistry: A Comprehensive Treatise. New York, Interscience Publishers. p. 1007.
  2. ^ Li, Guigen; Chang, Han-Ting; Sharpless, K. Barry (1996). "Catalytic Asymmetric Aminohydroxylation (AA) of Olefins". Angew. Chem. Int. Ed. Engl. 35 (4): 451–4. doi:10.1002/anie.199604511.
  3. ^ R. K. Murmann, C. L. Barnes "Redetermination of the crystal structure of potassium trans-(dioxo)-tetra(hydroxo)osmate(VI), K2[Os(OH)4(O)2]" Z. Kristallogr. NCS 217, 2002, pp. 303–304. doi:10.1524/ncrs.2002.217.jg.303
  4. ^ Frémy, E. "Ueber das Osmium" Journal für Praktische Chemie 1844 vol.33, 406-416. doi:10.1002/prac.18440330160
  5. ^ John M. Malin (1980). "Potassium Tetrahydroxodioxoosmate(VI) and trans ‐Bis(Ethylenediamine)Dioxoosmium(VI) Chloride". Potassium Tetrahydroxodioxoosmate(VI) and trans-Bis(Ethylenediamine)Dioxoosmium(VI) Chloride. Inorganic Syntheses. Vol. 20. pp. 61–63. doi:10.1002/9780470132517.ch18. ISBN 9780470132517.