Cyclopentadienyl anion

Cyclopentadienyl anion
Names
	IUPAC name Cyclopentadienide
Identifiers
CAS Number	12127-83-2;
3D model (JSmol)	Interactive image;
ChemSpider	2731064;
PubChem CID	3490527;
	InChI 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;
	SMILES [cH-]1cccc1;
Properties
Chemical formula	[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).
	Infobox references

Short description: Aromatic ionic species

In chemistry, the cyclopentadienyl anion or cyclopentadienide is an aromatic species with a formula of [C₅H₅]⁻ 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.^[2]

Resonance and aromaticity

Resonance structures of the cyclopentadienyl anion

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.^[3] The cyclopentadienyl anion is a conjugated system because there are alternating π and 𝜎 bonds.^[4]

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

Cyclopentadienyl anions form a variety of cyclopentadienyl complexes.^[5]

References

↑ "Cyclopentadienide". National Center for Biotechnology Information. https://pubchem.ncbi.nlm.nih.gov/compound/3490527#section=Top. Retrieved 14 April 2016.
↑ Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, p. 66, ISBN 978-0-471-72091-1, https://books.google.com/books?id=JDR-nZpojeEC&printsec=frontcover
↑ Paul, Satadal; Goswami, Tamal; Misra, Anirban (2015-10-01). "Noncomparative scaling of aromaticity through electron itinerancy". AIP Advances 5 (10): 107211. doi:10.1063/1.4933191. https://aip.scitation.org/doi/10.1063/1.4933191.
↑ "Delocalised electrons- Definition and Examples of Delocalized electrons with FAQs" (in en). https://byjus.com/chemistry/delocalized-electrons/.
↑ C. Elschenbroich (2006). Organometallics. VCH. ISBN 978-3-527-29390-2.

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[Cyclopentadienide-1] "Cyclopentadienide". National Center for Biotechnology Information. https://pubchem.ncbi.nlm.nih.gov/compound/3490527#section=Top. Retrieved 14 April 2016.

[2] Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, p. 66, ISBN 978-0-471-72091-1, https://books.google.com/books?id=JDR-nZpojeEC&printsec=frontcover

[3] Paul, Satadal; Goswami, Tamal; Misra, Anirban (2015-10-01). "Noncomparative scaling of aromaticity through electron itinerancy". AIP Advances 5 (10): 107211. doi:10.1063/1.4933191. https://aip.scitation.org/doi/10.1063/1.4933191.

[4] "Delocalised electrons- Definition and Examples of Delocalized electrons with FAQs" (in en). https://byjus.com/chemistry/delocalized-electrons/.

[5] C. Elschenbroich (2006). Organometallics. VCH. ISBN 978-3-527-29390-2.

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Cyclopentadienyl anion

Topic: Chemistry

Contents

Resonance and aromaticity

Ligand

See also

References