Lithium iodide
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Identifiers | |
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3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.030.735 |
PubChem CID
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UNII |
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CompTox Dashboard (EPA)
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Properties | |
LiI | |
Molar mass | 133.85 g/mol |
Appearance | White crystalline solid |
Density | 4.076 g/cm3 (anhydrous) 3.494 g/cm3 (trihydrate) |
Melting point | 469 °C (876 °F; 742 K) |
Boiling point | 1,171 °C (2,140 °F; 1,444 K) |
1510 g/L (0 °C) 1670 g/L (25 °C) 4330 g/L (100 °C) [1] | |
Solubility | soluble in ethanol, propanol, ethanediol, ammonia |
Solubility in methanol | 3430 g/L (20 °C) |
Solubility in acetone | 426 g/L (18 °C) |
−50.0·10−6 cm3/mol | |
Refractive index (nD)
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1.955 |
Thermochemistry | |
Heat capacity (C)
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0.381 J/g K or 54.4 J/mol K |
Std molar
entropy (S⦵298) |
75.7 J/mol K |
Std enthalpy of
formation (ΔfH⦵298) |
-2.02 kJ/g or −270.48 kJ/mol |
Gibbs free energy (ΔfG⦵)
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-266.9 kJ/mol |
Hazards | |
NFPA 704 (fire diamond) | |
Flash point | Non-flammable |
Safety data sheet (SDS) | External MSDS |
Related compounds | |
Other anions
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Lithium fluoride Lithium chloride Lithium bromide Lithium astatide |
Other cations
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Sodium iodide Potassium iodide Rubidium iodide Caesium iodide Francium iodide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Lithium iodide, or LiI, is a compound of lithium and iodine. When exposed to air, it becomes yellow in color, due to the oxidation of iodide to iodine.[2] It crystallizes in the NaCl motif.[3] It can participate in various hydrates.[4]
Applications
[edit]![](http://178.128.105.246/content-http-upload.wikimedia.org/wikipedia/commons/thumb/5/58/LiI%40DWNT.png/170px-LiI%40DWNT.png)
Lithium iodide is used as a solid-state electrolyte for high-temperature batteries. It is also the standard electrolyte in artificial pacemakers[6] due to the long cycle life it enables.[7] The solid is used as a phosphor for neutron detection.[8] It is also used, in a complex with Iodine, in the electrolyte of dye-sensitized solar cells.
In organic synthesis, LiI is useful for cleaving C-O bonds. For example, it can be used to convert methyl esters to carboxylic acids:[9]
- RCO2CH3 + LiI → RCO2Li + CH3I
Similar reactions apply to epoxides and aziridines.
Lithium iodide was used as a radiocontrast agent for CT scans. Its use was discontinued due to renal toxicity. Inorganic iodine solutions suffered from hyperosmolarity and high viscosities. Current iodinated contrast agents are organoiodine compounds.[10]
It is also useful in MALDI imaging mass spectrometry of lipids by adding lithium salts to the matrix solution
See also
[edit]References
[edit]- ^ Patnaik, Pradyot (2002) Handbook of Inorganic Chemicals. McGraw-Hill, ISBN 0-07-049439-8
- ^ "Lithium iodide" (PDF). ESPI Corp. MSDS. Archived from the original (PDF) on 2008-03-09. Retrieved 2005-09-16.
- ^ Wells, A.F. (1984) Structural Inorganic Chemistry, Oxford: Clarendon Press. ISBN 0-19-855370-6.
- ^ Wietelmann, Ulrich and Bauer, Richard J. (2005) "Lithium and Lithium Compounds" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH: Weinheim. doi:10.1002/14356007.a15_393.
- ^ Senga, Ryosuke; Suenaga, Kazu (2015). "Single-atom electron energy loss spectroscopy of light elements". Nature Communications. 6: 7943. Bibcode:2015NatCo...6.7943S. doi:10.1038/ncomms8943. PMC 4532884. PMID 26228378.
- ^ Holmes, C. (2007-09-28). "The Lithium/Iodine-Polyvinylpyridine Pacemaker Battery - 35 years of Successful Clinical Use". ECS Transactions. 6 (5): 1–7. Bibcode:2007ECSTr...6e...1H. doi:10.1149/1.2790382. ISSN 1938-5862. S2CID 138189063.
- ^ Hanif, Maryam (2008). "The Pacemaker Battery - Review Article". UIC Bioengineering Student Journal.
- ^ Nicholson, K. P.; et al. (1955). "Some lithium iodide phosphors for slow neutron detection". Br. J. Appl. Phys. 6 (3): 104–106. Bibcode:1955BJAP....6..104N. doi:10.1088/0508-3443/6/3/311.
- ^ Charette, André B.; Barbay, J. Kent and He, Wei (2005) "Lithium Iodide" in Encyclopedia of Reagents for Organic Synthesis, John Wiley & Sons. doi:10.1002/047084289X.rl121.pub2
- ^ Lusic, Hrvoje; Grinstaff, Mark W. (2013). "X-ray-Computed Tomography Contrast Agents". Chemical Reviews. 113 (3): 1641–66. doi:10.1021/cr200358s. PMC 3878741. PMID 23210836.
- ^ Petit, Cerruti; Touboul, Laprévote (2011). "MALDI imaging mass spectrometry of lipids by adding lithium salts to the matrix solution". Analytical and Bioanalytical Chemistry. 401 (1): 75–87. doi:10.1007/s00216-011-4814-9. PMC 3878741. PMID 21380605.
External links
[edit]![](http://178.128.105.246/content-http-upload.wikimedia.org/wikipedia/en/thumb/4/4a/Commons-logo.svg/30px-Commons-logo.svg.png)
- "WebElements – Lithium Iodide". Retrieved 2005-09-16.
- "Composition of Lithium Iodide – NIST". Retrieved 2006-02-03.