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Cyclopentadienyl radical

In chemistry, cyclopentadienyl is a radical with the formula C5H5.

Cyclopentadienyl radical
Names
Preferred IUPAC name
Cyclopenta-2,4-dien-1-yl[1]
Other names
Cyclopentadienyl[1]
Identifiers
  • 2143-53-5
3D model (JSmol)
  • Interactive image
2070324
ChEBI
  • CHEBI:36769
ChemSpider
  • 121110 Y
323080
  • 137443
  • DTXSID00175702
  • InChI=1S/C5H5/c1-2-4-5-3-1/h1-5H Y
    Key: HPYIUKIBUJFXII-UHFFFAOYSA-N Y
  • [CH]1C=CC=C1
Properties
C5H5
Molar mass 65.095 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

The related cyclopentadienyl anion (which can formally be converted to the cyclopentadienyl radical by one-electron reduction) is aromatic, and forms salts and coordination compounds.

See also edit

References edit

  1. ^ a b Henri A. Favre; Warren H. Powell (2014). Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013. Cambridge, England: The Royal Society of Chemistry. p. 1052. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.

cyclopentadienyl, radical, confused, with, cyclopentadienyl, anion, chemistry, cyclopentadienyl, radical, with, formula, c5h5, names, preferred, iupac, name, cyclopenta, dien, other, names, cyclopentadienyl, identifiers, number, 2143, model, jsmol, interactive. Not to be confused with Cyclopentadienyl anion In chemistry cyclopentadienyl is a radical with the formula C5H5 Cyclopentadienyl radical Names Preferred IUPAC name Cyclopenta 2 4 dien 1 yl 1 Other names Cyclopentadienyl 1 Identifiers CAS Number 2143 53 5 3D model JSmol Interactive image Beilstein Reference 2070324 ChEBI CHEBI 36769 ChemSpider 121110 Y Gmelin Reference 323080 PubChem CID 137443 CompTox Dashboard EPA DTXSID00175702 InChI InChI 1S C5H5 c1 2 4 5 3 1 h1 5H YKey HPYIUKIBUJFXII UHFFFAOYSA N Y SMILES CH 1C CC C1 Properties Chemical formula C 5H 5 Molar mass 65 095 g mol 1 Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa Infobox references The related cyclopentadienyl anion which can formally be converted to the cyclopentadienyl radical by one electron reduction is aromatic and forms salts and coordination compounds See also editCyclopentadienyl anion C5H5 Cyclopentadienyl cation C5H5 Cyclopentadiene C5H6 Methyl radical CH3 References edit a b Henri A Favre Warren H Powell 2014 Nomenclature of Organic Chemistry IUPAC Recommendations and Preferred Names 2013 Cambridge England The Royal Society of Chemistry p 1052 doi 10 1039 9781849733069 ISBN 978 0 85404 182 4 nbsp This organic chemistry article is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Cyclopentadienyl radical amp oldid 1220275756, wikipedia, wiki, book, books, library,

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