Lithium cyclopentadienide
Lithium cyclopentadienide is an organolithium compound with the formula C5H5Li. The compound is often abbreviated as LiCp, where Cp− is the cyclopentadienide anion. Lithium cyclopentadienide is a colorless solid, although samples often are pink owing to traces of oxidized impurities.
Names | |
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Other names
lithium cyclopentadienylide, cyclopentadienyllithium, LiCp | |
Identifiers | |
ECHA InfoCard | 100.156.001 |
PubChem CID |
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CompTox Dashboard (EPA) |
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Properties | |
C5H5Li | |
Molar mass | 72.04 g·mol−1 |
Appearance | colorless solid |
Density | 1.064 g/cm3 |
decomposition | |
Solubility | THF, dimethoxyethane |
Hazards | |
Main hazards | flammable |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Preparation, structure and reactions
Lithium cyclopentadienide is commercially available as a solution in THF. It is prepared by treating cyclopentadiene with butyllithium:[1]
- C5H6 + LiC4H9 → LiC5H5 + C4H10
Crystalline solvent-free LiCp, which is rarely encountered, is a "polydecker" sandwich complex, consisting of an infinite chain of alternating Li+ centers sandwiched between μ-η5:η5-C5H5 ligands.[2] In the presence of amines or ethers, LiCp gives adducts, e.g. (η5-Cp)Li(TMEDA).[1] LiCp is a common reagent for the preparation of cyclopentadienyl complexes.
See also
References
- Reent Michel, Regine Herbst-Irmer, Dietmar Stalke (2011). "Revealing Coordination Patterns in C5-Cyclic Lithium Organics". Organometallics. 30: 4379–4386. doi:10.1021/om200471e.CS1 maint: uses authors parameter (link)
- Robert E. Dinnebier; Ulrich Behrens & Falk Olbrich (1997). "Solid State Structures of Cyclopentadienyllithium, -sodium, and -potassium. Determination by High-Resolution Powder Diffraction". Organometallics. 16: 3855–3858. doi:10.1021/om9700122.