Sodium cyclopentadienide


Sodium cyclopentadienide is an organosodium compound with the formula C5H5Na. The compound is often abbreviated as NaCp, where Cp− is the cyclopentadienide anion. Sodium cyclopentadienide is a colorless solid, although samples often are pink owing to traces of oxidized impurities.

Preparation

Sodium cyclopentadienide is commercially available as a solution in THF. It is prepared by treating cyclopentadiene with sodium:
Commonly, the conversion is conducted by heating a suspension of molten sodium in dicyclopentadiene. In former times, the sodium was commonly provided in the form of "sodium wire" or "sodium sand", a fine dispersion of sodium prepared by melting sodium in refluxing xylene and rapidly stirring. Sodium hydride is a convenient base:
In early work, Grignard reagents were used as bases. With a pKa of 15, cyclopentadiene can be deprotonated by many reagents.

Applications

Sodium cyclopentadienide is a common reagent for the preparation of substituted cyclopentadienyl salts such as the ester and formyl compounds NaC5H4X :
Sodium cyclopentadienide is a common reagent for the preparation of metallocenes. For example, the preparation of ferrocene and zirconocene dichloride:

Structure

The nature of NaCp depends strongly on its medium and for the purposes of planning syntheses, the reagent is often represented as a salt. Crystalline solvent-free NaCp, which is rarely encountered, is a "polydecker" sandwich complex, consisting of an infinite chain of alternating Na+ centers sandwiched between μ-η5:η5-C5H5 ligands. As a solution in donor solvents, NaCp is highly solvated, especially at the alkali metal as suggested by the isolability of the adduct NaCp.
In contrast to alkali metal cyclopentadienides, tetrabutylammonium cyclopentadienide was found to be supported entirely by ionic bonding and its structure is representative of the structure of the cyclopentadienide anion in the solid state. However, the anion deviates somewhat from a planar, regular pentagon, with C–C bond lengths ranging from 138.0 -140.1 pm and C–C–C bond angles ranging from 107.5-108.8°.