Magnesium iodide
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Names | |||
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IUPAC name
Magnesium iodide
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Identifiers | |||
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3D model (JSmol)
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ChemSpider | |||
ECHA InfoCard | 100.030.738 | ||
EC Number |
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PubChem CID
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UNII |
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CompTox Dashboard (EPA)
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Properties | |||
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Molar mass |
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Appearance | white crystalline solid | ||
Odor | odorless | ||
Density |
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Melting point | 637 °C (1,179 °F; 910 K) (anhydrous, decomposes) 41 °C (octahydrate, decomposes) | ||
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Solubility | soluble in ether, alcohol and ammonia | ||
−111.0·10−6 cm3/mol | |||
Structure | |||
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Thermochemistry | |||
Heat capacity (C)
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74 J/(mol·K) | ||
Std molar
entropy (S⦵298) |
134 J/(mol·K) | ||
Std enthalpy of
formation (ΔfH⦵298) |
−364 kJ/mol | ||
Hazards | |||
GHS labelling: | |||
Warning | |||
H315, H319 | |||
NFPA 704 (fire diamond) | |||
Related compounds | |||
Other anions
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Other cations
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Magnesium iodide is an inorganic compound with the chemical formula MgI2. It forms various hydrates MgI2·xH2O. Magnesium iodide is a salt of magnesium and hydrogen iodide. These salts are typical ionic halides, being highly soluble in water.
Uses
[edit]Magnesium iodide has few commercial uses, but can be used to prepare compounds for organic synthesis.
Preparation
[edit]Magnesium iodide can be prepared from magnesium oxide, magnesium hydroxide, and magnesium carbonate by treatment with hydroiodic acid:[3]
Reactions
[edit]Magnesium iodide is stable at high heat under a hydrogen atmosphere, but decomposes in air at normal temperatures, turning brown from the release of elemental iodine. When heated in air, it decomposes completely to magnesium oxide.[4]
Another method to prepare MgI2 is mixing powdered elemental iodine and magnesium metal. In order to obtain anhydrous MgI2, the reaction should be conducted in a strictly anhydrous atmosphere; dry-diethyl ether can be used as a solvent.
Usage of magnesium iodide in the Baylis-Hillman reaction tends to give (Z)-vinyl compounds.[5]
Demethylation of certain aromatic methyl ethers can be afforded using magnesium iodide in diethyl ether.[6]
Hydrates
[edit]Two hydrates are known, the octahydrate and the nonahydrate, both verified by X-ray crystallography These hydrates feature [Mg(H2O)6]2+ ions.[7]
References
[edit]- ^ Perry, Dale L.; Phillips, Sidney L. (1995), Handbook of Inorganic Compounds, CRC Press, p. 240, ISBN 0-8493-8671-3, retrieved 2007-12-09
- ^ Magnesium Iodide MSDS at AlfaAesar[permanent dead link ]
- ^ Patnaik, Pradyot (2003), Handbook of Inorganic Chemicals, McGraw-Hill Professional, pp. 527–528, ISBN 0-07-049439-8, retrieved 2007-12-09
- ^ Wilsmore, N. T. M. (1891). "Note on Magnesium Iodide". In James Hector (ed.). Report of the Third Meeting of the Australasian Association for the Advancement of Science. Sydney: The Association. p. 116. Retrieved 2007-12-09.
- ^ Tietze, Lutz-Friedjan; Brasche, Gordon; Gericke, Kersten (2006), "Domino Reactions in Organic Synthesis", Chemical Reviews, 96 (1), Wiley-VCH: 115–136, doi:10.1021/cr950027e, ISBN 3-527-29060-5, PMID 11848746, retrieved 2007-12-09
- ^ Yamaguchi, Seiji; Nedachi, Masahiro; Yokoyama, Hajime; Hirai, Yoshiro (October 1999). "Regioselective demethylation of 2,6-dimethoxybenzaldehydes with magnesium iodide etherate". Tetrahedron Letters. 40 (41): 7363–7365. doi:10.1016/S0040-4039(99)01411-2.
- ^ Hennings, Erik; Schmidt, Horst; Voigt, Wolfgang (2013). "Crystal Structures of Hydrates of Simple Inorganic Salts. I. Water-Rich Magnesium Halide Hydrates MgCl2·8H2O, MgCl2·12H2O, MgBr2·6H2O, MgBr2·9H2O, MgI2·8H2O and MgI2·9H2O". Acta Crystallographica Section C Crystal Structure Communications. 69 (11): 1292–1300. doi:10.1107/S0108270113028138. PMID 24192174.