Dilithium acetylide
| LiC≡CLi | |
| Names | |
|---|---|
| Preferred IUPAC name Lithium acetylide | |
| Systematic IUPAC name Lithium ethynediide | |
| Other names 
 | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.012.710 | 
| EC Number | 
 | 
| PubChem CID | |
| UNII | |
| 
 | |
| 
 | |
| Properties | |
| Li2C2 | |
| Molar mass | 37.9034 g/mol | 
| Appearance | Powder | 
| Density | 1.3 g/cm3 | 
| Melting point | 452°C | 
| Reacts | |
| Solubility | insoluble in organic solvents | 
| Related compounds | |
| Related compounds | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Dilithium acetylide is an organometallic compound with the formula Li2C2. It is typically derived by double deprotonation of acetylene. X-ray crystallography confirms the presence of C≡C subunits attached to lithium, resulting in a polymeric structure. Li2C2 is one of an extensive range of lithium-carbon compounds, which include the lithium-rich Li4C, Li6C2, Li8C3, Li6C3, Li4C3, Li4C5, and the graphite intercalation compounds LiC6, LiC12, and LiC18. It is an intermediate compound produced during radiocarbon dating procedures.
Li2C2 is the most thermodynamically-stable lithium-rich carbide and the only one that can be obtained directly from the elements. It was first produced by Moissan, in 1896 who reacted coal with lithium carbonate.
- Li2CO3 + 4 C → Li2C2 + 3 CO
The other lithium-rich compounds are produced by reacting lithium vapor with chlorinated hydrocarbons, e.g. CCl4. Lithium carbide is sometimes confused with the drug lithium carbonate, Li2CO3, because of the similarity of its name.