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Nov. 2018/10/23 16:23:54 By LEAP Chem


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Basic Information of Ferrocene

Chemical Name: Ferrocene

Cas No.: 102-54-5

Molecular Formula: C10H10Fe

Chemical Structure:

 102-54-5.png

 

Ferrocene is an organometallic compound with the formula Fe(C5H5)2. It is the prototypical metallocene, a type of organometallic chemical compound consisting of two cyclopentadienyl rings bound on opposite sides of a central metal atom. Such organometallic compounds are also known as sandwich compounds. The rapid growth of organometallic chemistry is often attributed to the excitement arising from the discovery of ferrocene and its many analogues.

The first reported syntheses of ferrocene were nearly simultaneous. Pauson and Kealy synthesised ferrocene using iron(III) chloride and a Grignard reagent, cyclopentadienyl magnesium bromide. Iron(III) chloride is suspended in anhydrous diethyl ether and added to the Grignard reagent, which is prepared by reacting cyclopentadiene with magnesium and bromoethane in anhydrous benzene. An iron(III) salt was chosen as they sought to couple the cyclopentadienyl moieties to form dihydrofulvalene and then fulvalene, but ferrocene was formed instead as the oxidative formation of dihydrofulvalene also produced iron(II) by reduction, which in turn reacts with the Grignard.

Ferrocene undergoes many reactions characteristic of aromatic compounds, enabling the preparation of substituted derivatives. A common undergraduate experiment is the Friedel-Crafts reaction of ferrocene with acetic anhydride (or acetyl chloride) in the presence of phosphoric acid as a catalyst.

Ferrocene, a precursor to iron nanoparticles, can be used as a catalyst for the production of carbon nanotubes. The vinylferrocene can be made by a Wittig reaction of the aldehyde, a phosphonium salt, and sodium hydroxide. The vinyl ferrocene can be converted into a polymer (polyvinylferrocene, PVFc), a ferrocenyl version of polystyrene (the phenyl groups are replaced with ferrocenyl groups). Another polyferrocene which can be formed is poly(2-(methacryloyloxy)ethyl ferrocenecarboxylate), PFcMA. In addition to using organic polymer backbones, these pendant ferrocene units have been attached to inorganic backbones such as polysiloxanes, polyphosphazenes, and polyphosphinoboranes, (–PH(R)–BH2–)n, and the resulting materials exhibit unusual physical and electronic properties relating to the ferrocene / ferrocinium redox couple. Both PVFc and PFcMA have been tethered onto silica wafers and the wettability measured when the polymer chains are uncharged and when the ferrocene moieties are oxidised to produce positively charged groups. The contact angle with water on the PFcMA-coated wafers was 70° smaller following oxidation, while in the case of PVFc the decrease was 30°, and the switching of wettability is reversible. In the PFcMA case, the effect of lengthening the chains and hence introducing more ferrocene groups is significantly larger reductions in the contact angle upon oxidation.

 

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References:

https://en.wikipedia.org/wiki/Ferrocene

https://www.ncbi.nlm.nih.gov/pubmed/15584693

https://www.ncbi.nlm.nih.gov/pubmed/18666277

 

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