Cyclopentadienyl anion explained

In chemistry, the cyclopentadienyl anion or cyclopentadienide is an aromatic species with a formula of and abbreviated as Cp-.[1] It is formed by the deprotonation of cyclopentadiene. The cyclopentadienyl anion is a ligand which binds to a metal in organometallic chemistry.

Resonance and aromaticity

See also: Sodium cyclopentadienide. The cyclopentadienyl anion is a planar, cyclic, regular-pentagonal ion; it has 6 π-electrons (4n + 2, where n = 1), which fulfills Hückel's rule of aromaticity. Each double bond and lone pair provides 2 π-electrons, which are delocalized into the ring.[2]

Cyclopentadiene has a pKa of about 16. It is acidic relative to many carbon acids. The enhanced acidity is attributed to stabilization of the conjugate base, cyclopentadienyl anion.

Ligand

See main article: Cyclopentadienyl complex. Cyclopentadienyl anions form a variety of cyclopentadienyl complexes.[3]

See also

Notes and References

  1. Web site: Cyclopentadienide. PubChem Compound Database. National Center for Biotechnology Information. 14 April 2016.
  2. Paul . Satadal . Goswami . Tamal . Misra . Anirban . 2015-10-01 . Noncomparative scaling of aromaticity through electron itinerancy . AIP Advances . 5 . 10 . 107211 . 10.1063/1.4933191. free .
  3. Book: Organometallics. C. Elschenbroich. VCH. 2006. 978-3-527-29390-2.