Cyclopentadienyl anion

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Cyclopentadienyl anion
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C5H5/c1-2-4-5-3-1/h1-5H/q-1
    Key: SINKOGOPEQSHQD-UHFFFAOYSA-N
  • InChI=1/C5H5/c1-2-4-5-3-1/h1-5H/q-1
    Key: SINKOGOPEQSHQD-UHFFFAOYAD
  • [cH-]1cccc1
Properties
[C5H5] or Cp
Molar mass 65.09 g/mol
Conjugate acid Cyclopentadiene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

In chemistry, the cyclopentadienyl anion or cyclopentadienide is an aromatic species with a formula of [C5H5] and abbreviated as Cp.[1] Its name derives from the molecule cyclopentadiene.

It is a regular pentagonal, planar, cyclic ion; as well, it has 6 π-electrons (4n + 2, where n = 1), which fulfills Hückel's rule of aromaticity. It can coordinate as a ligand to metal atoms.

The structure shown is a composite of five resonance contributors in which each carbon atom carries part of the negative charge.

Salts of the cyclopentadienyl anion can be stable, e.g., sodium cyclopentadienide.

Coordination compounds of the cyclopentadienyl anion (not the cyclopentadienyl radical) are known as cyclopentadienyl complexes. Biscyclopentadienyl complexes are called metallocenes.

See also

References

  1. ^ "Cyclopentadienide". PubChem Compound Database. National Center for Biotechnology Information. Retrieved 14 April 2016.