Lithium perchlorate
Lithium perchlorate | |
---|---|
IUPAC name Lithium perchlorate | |
Other names Perchloric acid, lithium salt; Lithium Cloricum | |
Identifiers | |
CAS number | 7791-03-9 |
PubChem | 23665649 |
ChemSpider | 133514 |
Jmol-3D images | {{#if:[Li+].[O-]Cl(=O)(=O)=O|Image 1 |
| |
| |
Properties | |
Molecular formula | LiClO4 |
Molar mass | 106.392 g/mol |
Appearance | white crystals |
Odor | odorless |
Density | 2.42 g/cm3, solid |
Melting point | 236 °C |
Boiling point | 430 °C (with decomp.) |
Solubility in water | 60 g/100 mL |
Solubility in organic solvents | Soluble |
Thermochemistry | |
Std enthalpy of formation ΔfH |
-3.581 kJ/g or -380.99 kJ/mol |
Hazards | |
MSDS | MSDS |
Main hazards | Oxidizer, irritant |
NFPA 704 |
0
2
0
OX
|
Related compounds | |
Other anions | Lithium chloride Lithium hypochlorite Lithium chlorate |
Other cations | Sodium perchlorate Potassium perchlorate Rubidium perchlorate |
(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 | |
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.
Uses
Lithium perchlorate is used as a source of oxygen in some chemical oxygen generators. It decomposes at about 400 °C, yielding lithium chloride and oxygen, the latter being over 60% of its mass. It has both the highest oxygen to weight and oxygen to volume ratio of all perchlorates, except beryllium diperchlorate (which is expensive and highly toxic).
LiClO4 is highly soluble in organic solvents, even diethyl ether. Such solutions are employed in Diels-Alder reactions, where it is proposed that the Lewis acidic Li+ binds to Lewis basic sites on the dienophile, thereby accelerating the reaction.[1]
Lithium perchlorate is also used as an inert electrolyte in lithium batteries.
Concentrated solutions of lithium perchlorate (4.5 mol/l) are used as a chaotropic agent to denature proteins.
Lithium perchlorate is also used as a co-catalyst in the coupling of α,β-unsaturated carbonyls with aldehydes, also known as the Baylis-Hillman reaction.[2]
Production
Lithium perchlorate can be manufactured by reaction of sodium perchlorate with lithium chloride. It can be also prepared by electrolysis of lithium chlorate at 200 mA/cm² at temperatures above 20 °C.[3]
Safety
Perchlorates often give explosive mixtures with organic compounds.[3]
External links
References
- ↑ Charette, A. B. "Lithium Perchlorate" in Encyclopedia of Reagents for Organic Synthesis (Ed: L. Paquette) 2004, J. Wiley & Sons, New York. doi:10.1002/047084289.
- ↑ Lithium Perchlorate Product Detail Page
- ↑ 3.0 3.1 Helmut Vogt, Jan Balej, John E. Bennett, Peter Wintzer, Saeed Akbar Sheikh, Patrizio Gallone "Chlorine Oxides and Chlorine Oxygen Acids" in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH. doi:10.1002/14356007.a06_483
|