Lithium iodide

Last updated
Lithium iodide
NaCl polyhedra.png
__ Li +     __ I
Lithium-iodide-3D-ionic.png
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.030.735 OOjs UI icon edit-ltr-progressive.svg
PubChem CID
UNII
  • InChI=1S/HI.Li/h1H;/q;+1/p-1 Yes check.svgY
    Key: HSZCZNFXUDYRKD-UHFFFAOYSA-M Yes check.svgY
  • InChI=1/HI.Li/h1H;/q;+1/p-1
    Key: HSZCZNFXUDYRKD-REWHXWOFAM
  • [Li+].[I-]
Properties
LiI
Molar mass 133.85 g/mol
AppearanceWhite 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
Std molar
entropy
(S298)
75.7 J/mol K
-2.02 kJ/g or −270.48 kJ/mol
-266.9 kJ/mol
Hazards
NFPA 704 (fire diamond)
NFPA 704.svgHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
0
0
Flash point Non-flammable
Safety data sheet (SDS) External MSDS
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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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]

Contents

Applications

LiI chains grown inside double-wall carbon nanotubes. LiI@DWNT.png
LiI chains grown inside double-wall carbon nanotubes.

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

Related Research Articles

<span class="mw-page-title-main">Hydride</span> Molecule with a hydrogen bound to a more electropositive element or group

In chemistry, a hydride is formally the anion of hydrogen (H), a hydrogen atom with two electrons. The term is applied loosely. At one extreme, all compounds containing covalently bound H atoms are called hydrides: water (H2O) is a hydride of oxygen, ammonia is a hydride of nitrogen, etc. For inorganic chemists, hydrides refer to compounds and ions in which hydrogen is covalently attached to a less electronegative element. In such cases, the H centre has nucleophilic character, which contrasts with the protic character of acids. The hydride anion is very rarely observed.

<span class="mw-page-title-main">Lithium aluminium hydride</span> Chemical compound

Lithium aluminium hydride, commonly abbreviated to LAH, is an inorganic compound with the chemical formula Li[AlH4] or LiAlH4. It is a white solid, discovered by Finholt, Bond and Schlesinger in 1947. This compound is used as a reducing agent in organic synthesis, especially for the reduction of esters, carboxylic acids, and amides. The solid is dangerously reactive toward water, releasing gaseous hydrogen (H2). Some related derivatives have been discussed for hydrogen storage.

In organic chemistry, an aryl halide is an aromatic compound in which one or more hydrogen atoms, directly bonded to an aromatic ring are replaced by a halide. The haloarene are different from haloalkanes because they exhibit many differences in methods of preparation and properties. The most important members are the aryl chlorides, but the class of compounds is so broad that there are many derivatives and applications.

<span class="mw-page-title-main">Thionyl chloride</span> Inorganic compound (SOCl2)

Thionyl chloride is an inorganic compound with the chemical formula SOCl2. It is a moderately volatile, colourless liquid with an unpleasant acrid odour. Thionyl chloride is primarily used as a chlorinating reagent, with approximately 45,000 tonnes per year being produced during the early 1990s, but is occasionally also used as a solvent. It is toxic, reacts with water, and is also listed under the Chemical Weapons Convention as it may be used for the production of chemical weapons.

<span class="mw-page-title-main">Ammonium iodide</span> Chemical compound

Ammonium iodide is the inorganic compound with the formula NH4I. A white solid. It is an ionic compound, although impure samples appear yellow. This salt consists of ammonium cation and an iodide anion. It can be prepared by the action of hydroiodic acid on ammonia. It is easily soluble in water, from which it crystallizes in cubes. It is also soluble in ethanol. Ammonium iodide in aqueous solutions are observed as acidic and display elevated vapor pressures at high temperatures

<span class="mw-page-title-main">Sodium iodide</span> Chemical compound

Sodium iodide (chemical formula NaI) is an ionic compound formed from the chemical reaction of sodium metal and iodine. Under standard conditions, it is a white, water-soluble solid comprising a 1:1 mix of sodium cations (Na+) and iodide anions (I) in a crystal lattice. It is used mainly as a nutritional supplement and in organic chemistry. It is produced industrially as the salt formed when acidic iodides react with sodium hydroxide. It is a chaotropic salt.

<span class="mw-page-title-main">Lithium perchlorate</span> Chemical compound

Lithium perchlorate is the inorganic compound with the formula LiClO4. This white or colourless crystalline salt is noteworthy for its high solubility in many solvents. It exists both in anhydrous form and as a trihydrate.

<span class="mw-page-title-main">Lithium fluoride</span> Chemical compound

Lithium fluoride is an inorganic compound with the chemical formula LiF. It is a colorless solid that transitions to white with decreasing crystal size. Although odorless, lithium fluoride has a bitter-saline taste. Its structure is analogous to that of sodium chloride, but it is much less soluble in water. It is mainly used as a component of molten salts. Partly because Li and F are both light elements, and partly because F2 is highly reactive, formation of LiF from the elements releases one of the highest energies per mass of reactants, second only to that of BeO.

<span class="mw-page-title-main">Copper(I) iodide</span> Chemical compound

Copper(I) iodide is the inorganic compound with the formula CuI. It is also known as cuprous iodide. It is useful in a variety of applications ranging from organic synthesis to cloud seeding.

<span class="mw-page-title-main">Phosphorus pentasulfide</span> Chemical compound

Phosphorus pentasulfide is the inorganic compound with the formula P2S5 (empirical) or P4S10 (molecular). This yellow solid is the one of two phosphorus sulfides of commercial value. Samples often appear greenish-gray due to impurities. It is soluble in carbon disulfide but reacts with many other solvents such as alcohols, DMSO, and DMF.

<span class="mw-page-title-main">Nickel(II) iodide</span> Chemical compound

Nickel(II) iodide is an inorganic compound with the formula NiI2. This paramagnetic black solid dissolves readily in water to give bluish-green solutions, from which crystallizes the aquo complex [Ni(H2O)6]I2 (image above). This bluish-green colour is typical of hydrated nickel(II) compounds. Nickel iodides find some applications in homogeneous catalysis.

<span class="mw-page-title-main">Hexamethyldisilane</span> Chemical compound

Hexamethyldisilane (TMS2) is the organosilicon compound with the formula Si2(CH3)6, abbreviated Si2Me6. It is a colourless liquid, soluble in organic solvents.

<span class="mw-page-title-main">Lithium tetrafluoroborate</span> Chemical compound

Lithium tetrafluoroborate is an inorganic compound with the formula LiBF4. It is a white crystalline powder. It has been extensively tested for use in commercial secondary batteries, an application that exploits its high solubility in nonpolar solvents.

Organoiodine chemistry is the study of the synthesis and properties of organoiodine compounds, or organoiodides, organic compounds that contain one or more carbon–iodine bonds. They occur widely in organic chemistry, but are relatively rare in nature. The thyroxine hormones are organoiodine compounds that are required for health and the reason for government-mandated iodization of salt.

<span class="mw-page-title-main">Titanium disulfide</span> Inorganic chemical compound

Titanium disulfide is an inorganic compound with the formula TiS2. A golden yellow solid with high electrical conductivity, it belongs to a group of compounds called transition metal dichalcogenides, which consist of the stoichiometry ME2. TiS2 has been employed as a cathode material in rechargeable batteries.

<span class="mw-page-title-main">NASICON</span>

NASICON is an acronym for sodium (Na) Super Ionic CONductor, which usually refers to a family of solids with the chemical formula Na1+xZr2SixP3−xO12, 0 < x < 3. In a broader sense, it is also used for similar compounds where Na, Zr and/or Si are replaced by isovalent elements. NASICON compounds have high ionic conductivities, on the order of 10−3 S/cm, which rival those of liquid electrolytes. They are caused by hopping of Na ions among interstitial sites of the NASICON crystal lattice.

Cerium(III) iodide (CeI3) is the compound formed by cerium(III) cations and iodide anions.

<span class="mw-page-title-main">Solid-state electrolyte</span>

A solid-state electrolyte (SSE) is a solid ionic conductor and electron-insulating material and it is the characteristic component of the solid-state battery. It is useful for applications in electrical energy storage (EES) in substitution of the liquid electrolytes found in particular in lithium-ion battery. The main advantages are the absolute safety, no issues of leakages of toxic organic solvents, low flammability, non-volatility, mechanical and thermal stability, easy processability, low self-discharge, higher achievable power density and cyclability. This makes possible, for example, the use of a lithium metal anode in a practical device, without the intrinsic limitations of a liquid electrolyte thanks to the property of lithium dendrite suppression in the presence of a solid-state electrolyte membrane. The use of a high capacity anode and low reduction potential, like lithium with a specific capacity of 3860 mAh g−1 and a reduction potential of -3.04 V vs SHE, in substitution of the traditional low capacity graphite, which exhibits a theoretical capacity of 372 mAh g−1 in its fully lithiated state of LiC6, is the first step in the realization of a lighter, thinner and cheaper rechargeable battery. Moreover, this allows the reach of gravimetric and volumetric energy densities, high enough to achieve 500 miles per single charge in an electric vehicle. Despite the promising advantages, there are still many limitations that are hindering the transition of SSEs from academia research to large-scale production, depending mainly on the poor ionic conductivity compared to that of liquid counterparts. However, many car OEMs (Toyota, BMW, Honda, Hyundai) expect to integrate these systems into viable devices and to commercialize solid-state battery-based electric vehicles by 2025.

Antimonide iodides or iodide antimonides are compounds containing anions composed of iodide (I) and antimonide (Sb3−). They can be considered as mixed anion compounds. They are in the category of pnictide halides. Related compounds include the antimonide chlorides, antimonide bromides, phosphide iodides, and arsenide iodides.

References

  1. Patnaik, Pradyot (2002) Handbook of Inorganic Chemicals. McGraw-Hill, ISBN   0-07-049439-8
  2. "Lithium iodide" (PDF). ESPI Corp. MSDS. Archived from the original (PDF) on 2008-03-09. Retrieved 2005-09-16.
  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. Bibcode:2015NatCo...6.7943S. doi:10.1038/ncomms8943. PMC   4532884 . PMID   26228378.
  6. 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.
  7. Hanif, Maryam (2008). "The Pacemaker Battery - Review Article". UIC Bioengineering Student Journal.
  8. 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.
  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. PMC   3878741 . PMID   23210836.