Chemistry:Lithium iodide

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Lithium iodide
Lithium iodide
__ Li+     __ I
Lithium-iodide-3D-ionic.png
Identifiers
3D model (JSmol)
ChemSpider
UNII
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
1.955
Thermochemistry
0.381 J/g K or 54.4 J/mol K
75.7 J/mol K
-2.02 kJ/g or −270.48 kJ/mol
-266.9 kJ/mol
Hazards
Safety data sheet External MSDS
NFPA 704 (fire diamond)
Flammability code 0: Will not burn. E.g. waterHealth code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no codeNFPA 704 four-colored diamond
0
2
0
Flash point Non-flammable
Related compounds
Other anions
Lithium fluoride
Lithium chloride
Lithium bromide
Lithium astatide
Other cations
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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Infobox references

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

LiI chains grown inside double-wall carbon nanotubes.[5]

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]

See also

References

  1. Patnaik, Pradyot (2002) Handbook of Inorganic Chemicals. McGraw-Hill, ISBN:0-07-049439-8
  2. "Lithium iodide". ESPI Corp. MSDS. http://www.espimetals.com/msds's/lithiumiodide.pdf. 
  3. Wells, A.F. (1984) Structural Inorganic Chemistry, Oxford: Clarendon Press. ISBN:0-19-855370-6.
  4. 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.
  5. Senga, Ryosuke; Suenaga, Kazu (2015). "Single-atom electron energy loss spectroscopy of light elements". Nature Communications 6: 7943. doi:10.1038/ncomms8943. PMID 26228378. Bibcode2015NatCo...6.7943S. 
  6. Holmes, C. (2007-09-28). "The Lithium/Iodine-Polyvinylpyridine Pacemaker Battery - 35 years of Successful Clinical Use" (in en). ECS Transactions 6 (5): 1–7. doi:10.1149/1.2790382. ISSN 1938-5862. Bibcode2007ECSTr...6e...1H. https://iopscience.iop.org/article/10.1149/1.2790382/meta. 
  7. Hanif, Maryam (2008). "The Pacemaker Battery - Review Article". UIC Bioengineering Student Journal. 
  8. Nicholson, K. P. (1955). "Some lithium iodide phosphors for slow neutron detection". Br. J. Appl. Phys. 6 (3): 104–106. doi:10.1088/0508-3443/6/3/311. Bibcode1955BJAP....6..104N. 
  9. 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
  10. Lusic, Hrvoje; Grinstaff, Mark W. (2013). "X-ray-Computed Tomography Contrast Agents". Chemical Reviews 113 (3): 1641–66. doi:10.1021/cr200358s. PMID 23210836. 

External links

HI He
LiI BeI2 BI3 CI4 NI3 I2O4,
I2O5,
I4O9
IF,
IF3,
IF5,
IF7
Ne
NaI MgI2 AlI3 SiI4 PI3,
P2I4
S ICl,
ICl3
Ar
KI CaI2 Sc TiI4 VI3 CrI3 MnI2 FeI2 CoI2 NiI2 CuI ZnI2 Ga2I6 GeI2,
GeI4
AsI3 Se IBr Kr
RbI SrI2 YI3 ZrI4 NbI5 Mo Tc Ru Rh Pd AgI CdI2 InI3 SnI4,
SnI2
SbI3 TeI4 I Xe
CsI BaI2   HfI4 TaI5 W Re Os Ir Pt AuI Hg2I2,
HgI2
TlI PbI2 BiI3 Po AtI Rn
Fr RaI2   Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
La Ce Pr Nd Pm SmI2 Eu Gd TbI3 Dy Ho Er Tm Yb Lu
Ac ThI4 Pa UI3,
UI4
Np Pu Am Cm Bk Cf EsI3 Fm Md No Lr