Triosmium dodecacarbonyl
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| Triosmium dodecacarbonyl | |
|---|---|
| Image:Triosmium dodecacarbonyl.jpg | |
| General | |
| Systematic name | Triosmium dodecarbonyl |
| Other names | Osmium carbonyl |
| Molecular formula | C12O12Os3 |
| SMILES | ? |
| Molar mass | 906.81 g/mol |
| Appearance | yellow solid |
| CAS number | [15696-40-9] |
| Properties | |
| Density and phase | 3.48 g/cm3 |
| Solubility in water | insoluble |
| Other solvents | slightly in organic solvents |
| Melting point | 224 °C |
| Boiling point | sublimes in vacuum |
| Structure | |
| Molecular structure | D3h cluster |
| Crystal structure | |
| Dipole moment | 0 D (0 C·m) |
| Hazards | |
| MSDS | External MSDS |
| Main hazards | CO source |
| NFPA 704 | |
| R/S statement | R: 22-36/37/38 S: 22-26-36/37/39 |
| Supplementary data page | |
| Structure and properties |
n, εr, etc. |
| Thermodynamic data |
Phase behaviour Solid, liquid, gas |
| Spectral data | IR: 2070, 2036, 2003 cm-1 (hexane solution) |
| Related compounds | |
| Related compounds | Fe3(CO)12 Ru3(CO)12 Decacarbonyldihydridotriosmium |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
|
Triosmium dodecarbonyl is a chemical compound with the formula Os3(CO)12. This yellow colored metal carbonyl cluster is an important precursor to organo-osmium compounds. Many of the advances in cluster chemistry have arisen from studies on derivatives of Os3(CO)12 and its lighter analogue Ru3(CO)12.
[edit] Structure and synthesis
The cluster has D3h symmetry, consisting of an equilateral triangle of Os atoms, each of which bears two axial and two equatorial CO ligands. The Os–Os bond distance is 2.88 Â (288 pm).[1] Ru3(CO)12 has the same structure, whereas Fe3(CO)12 is different, with two bridging CO ligands resulting in C2v symmetry.
Os3(CO)12 is prepared by the direct reaction of OsO4 with carbon monoxide at 175 °C:[2]
- 3 OsO4 + 24 CO → Os3(CO)12 + 12 CO2
The yield is nearly quantitative.
[edit] Reactions
The chemical properties of Os3(CO)12 have been thoroughly examined. Direct reactions of ligands with the cluster often lead to complex product distributions because the inert Os–CO bonds require high temperatures to break, and at such high temperatures successive the initially formed adducts react further. More successfully, Os3(CO)12 is converted to more labile derivatives such as Os3(CO)11(MeCN) and Os3(CO)10(MeCN)2 using Me3NO as a decarbonylation agent.[3] Os3(CO)11(MeCN) reacts with a variety of even weakly basic ligands to form adducts such as Os3(CO)11(ethylene) and Os3(CO)11(pyridine). The direct reaction of Os3(CO)12 with ethylene and pyridine results in degradation of these organic ligands to give the vinyl hydride HOs3(CO)10(η1,η2-C2H3) and the pyridyl-hydride HOs3(CO)10(NC5H4). These products illustrate the stability of Os–H and Os–C bonds.
Os3(CO)12 is a platform to examine the ways that hydrocarbons can interact with ensembles of metals. For example, in Fischer-Tropsch processing, it is understood that the polymetallic catalysts assist the hydrogenation of CO to give hydrocarbons. Models for such intermediates are provided by the series CH3(H)Os3(CO)10, (CH2)(H)2Os3(CO)10, and (CH)(H)3Os3(CO)9.[4] The molecule CH3(H)Os3(CO)10 provided one of the first clear-cut examples of agostic bonding.[5]
From the perspective of bonding, the molecule H2Os3(CO)10 is noteworthy. In this compound, the two hydride ligands bridge one Os-Os edge. The molecule displays reactivity reminiscent of diborane.[6]
[edit] References
- ^ Corey, E. R.; Dahl, L. F. “The Molecular and Crystal Structure of Os3(CO)12” Inorganic Chemistry 1962, volume 1, pages 521 - 526. DOI: 10.1021/ic50003a016
- ^ Drake, S. R.; Loveday, P. A. “Dodecarbonyltriosmium” Inorganic Syntheses, 1990, volume 28, pages 230-1. ISBN 0-471-52619-3.
- ^ Nicholls, J. N.; Vargas, M. D. “Some Useful Derivatives of Dodecarbonyltriosmium” Inorganic Syntheses, 1990, volume 28, pages 232-5. ISBN 0-471-52619-3.
- ^ Calvert, R. B.; Shapley, J. R. “Activation of Hydrocarbons by Unsaturated Metal Cluster Complexes. 6. Synthesis and Characterization of Methyldecacarbonylhydridotriosmium, Methylenedecacarbonyldihydridotriosmium, and Methylidynenonacarbonyltrihydridotriosmium. Interconversion of Cluster-Bound Methyl and Methylene Ligands” Journal of the American Chemical Society 1977, volume 99, 5225-6. DOI: 10.1021/ja00457a077
- ^ Calvert, R. B.; Shapley, J. R. “Decacarbonyl(methyl)hydrotriosmium: NMR evidence for a Carbon..Hydrogen..Osmium Interaction” Journal of the American Chemical Society 1978, volume 100, pages 7726-7. DOI: 10.1021/ja00492a047
- ^ Keister, J. B.; Shapley, J. R. “Solution Structures and Dynamics of complexes of Decacarbonyldihydrotriosmium with Lewis Bases” Inorganic Chemistry 1982, volume 21, pages 3304-10.DOI: 10.1021/ic00139a011DOI: 10.1021/ic00139a011
