Cyclopentadienyliron dicarbonyl iodide
| Cyclopentadienyliron dicarbonyl iodide | ||
|---|---|---|
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| Identifiers | ||
| CAS number | 12078-28-3  | |
| Properties | ||
| Molecular formula | C7H5FeIO2 | |
| Molar mass | 303.86 g mol−1 | |
| Appearance | Dark brown crystalline | |
| Melting point | 119 °C; 246 °F; 392 K | |
| Structure | ||
| Space group | Cs | |
| Hazards | ||
| MSDS | [http://www.sigmaaldrich.com/MSDS/MSDS/DisplayMSDSPage.do?country=US&language=en&productNumber=251119&brand=ALDRICH&PageToGoToURL=http%3A%2F%2Fwww.sigmaaldrich.com%2Fcatalog%2Fsearch%3Finterface%3DCAS%2520No.%26term%3D12078-28-3%26lang%3Den%26region%3DUS%26focus%3Dproduct%26N%3D0%2B220003048%2B219853269%2B219853286%26mode%3Dpartialmax%26F%3DPR%26ST%3DRS%26N3%3Dmode%2520matchpartialmax%26N5%3DCAS%2520No. Here] | |
(verify) (what is: / ?)Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | ||
| Infobox references | ||
Cyclopentadienyliron dicarbonyl iodide is an organoiron compound with the formula (C5H5)Fe(CO)2I. It is a dark brown solid that is soluble in common organic solvents. (C5H5)Fe(CO)2I, or FpI as it is often known, is an intermediate for the preparation of other organoironc compounds such as in ferraboranes.
Preparation
Cyclopentadienyliron dicarboxnl iodide is synthesized by the reaction of cyclopentadienyliron dicarbonyl dimer with I2:
- Cp2Fe2(CO)4 + I2 → 2 CpFe(CO)2I
It was probably first reported by Paulson and Hallam.[1]
Structure
The compound has Cs symmetry, with a mirror plane intersecting one carbon of the Cp ring as well as the iron and iodide centre. The compound adopts a piano stool structure: the cyclopentadienyl ligand is the "seat" and three other ligands are "legs". Such compounds are members of the half-sandwich family of compounds, which is a subgroup of the metallocenes. X-ray crystallography shows the following features: Fe-Cp centroid = 1.72, Fe-I = 2.61, and Fe-CO = 1.78 Å.[2]
Electron counting of this ferrous complex indicates 6 electrons from the cyclopentadienyl anion, 2 electron from each of the carbonyls, and 2 electrons from the iodide.
References
- ↑ B. F. Hallam, P. L. Paulson "Ferrocene Derivatives. Part III. Cyclopentadienyliron Carbonyls" J. Chem. Soc. 1956, pp. 3031-3037.
- ↑ Zeller, M.; Lazich, E.; Hunter, A. D. (2003). "Dicarbonyl(η5-cyclopentadienyl)iodoiron(II)". Acta Crystallogr., Sect. E 59: m914–m915. doi:10.1107/S1600536803019950.