Structure via PubChem · Public domain (PubChem)
ferrocene
Sign in to saveAlso known as Dicyclopentadienyl iron, bis(Cyclopentadienyl)iron, Iron dicyclopentadienyl
Chemical data
- Formula
- C10H10Fe-6
- Molecular weight
- 186.03 g/mol
- IUPAC name
- cyclopenta-1,3-diene;cyclopentane;iron
- SMILES
- [CH-]1[CH-][CH-][CH-][CH-]1.[CH-]1C=CC=C1.[Fe]
- InChIKey
- XISWFGALECMDCV-UHFFFAOYSA-N
- Polar surface area
- 0 Ų
- H-bond donors
- 0
- H-bond acceptors
- 6
- Formal charge
- -6
via PubChem
Wikidata facts
- Mass
- 186.013
- Image
- Ferrocene Crystals.png
Show 9 more facts
- Commons category
- Ferrocene
- chemical formula
- C₁₀H₁₀Fe
- time-weighted average exposure limit
- 15
- NIOSH Pocket Guide ID
- 0205
- time of discovery or invention
- 1951-00-00
- melting point
- 343
- boiling point
- 480
- ionization energy
- 6.88
- canonical SMILES
- [CH-]1C=CC=C1.[CH-]1C=CC=C1.[Fe+2]
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~20 min read
Article
23 sectionsContents
- History
- Discovery
- Determining the structure
- Impact
- Structure and bonding
- Synthesis
- Early methods
- Via alkali cyclopentadienide
- Reactions
- Aromatic substitution
- Metallation
- Redox chemistry
- Stereochemistry of substituted ferrocenes
- Applications of ferrocene and its derivatives
- Ligand scaffolds
- Fuel additives
- Pharmaceuticals
- Solid rocket propellant
- Derivatives and variations
- Materials chemistry
- See also
- References
- External links
Ferrocene is an organometallic compound with the formula . The molecule is a cyclopentadienyl complex consisting of two cyclopentadienyl rings sandwiching a central iron atom. It is an orange solid with a camphor-like odor that sublimes above room temperature, and is soluble in most organic solvents. It is remarkable for its stability: it is unaffected by air, water, or strong bases, and can be heated to without decomposition. In oxidizing conditions it can reversibly react with strong acids to form the ferrocenium cation .
The first reported synthesis of ferrocene was in 1951. Its unusual stability puzzled chemists, and required the development of new theory to explain its formation and bonding. The discovery of ferrocene and its many structural analogues, known as metallocenes, sparked excitement and led to a rapid growth in the discipline of organometallic chemistry. Geoffrey Wilkinson and Ernst Otto Fischer, both of whom worked on elucidating the structure of ferrocene, later shared the 1973 Nobel Prize in Chemistry for their work on organometallic sandwich compounds. Ferrocene itself has no large-scale applications, but has found more niche uses in catalysis, as a fuel additive, as an internal standard in electrochemical research, and as a tool in undergraduate education.