Vinylferrocene

Vinylferrocene is the organometallic compound with the formula (C5H5)Fe(C5H4CH=CH2). It is a derivative of ferrocene, with a vinyl group attached to one cyclopentadienyl ligand. As the ferrocene analogue of styrene, it is the precursor to some polyferrocenes.[1] It is an orange, air-stable oily solid that is soluble in nonpolar organic solvents.

Vinylferrocene
Identifiers
3D model (JSmol)
ChemSpider
Properties
C12H12Fe
Molar mass 212.073 g·mol−1
Appearance orange solid
Melting point 50–52 °C (122–126 °F; 323–325 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Vinylferrocene can be prepared by the dehydration of α-hydroxylethylferrocene, which is obtained from acetylferrocene.[2]

References

  1. Cass, Anthony E. G.; Davis, Graham; Francis, Graeme D.; Hill, H. Allen O.; Aston, William J.; Higgins, I. John; Plotkin, Elliot V.; Scott, Lesley D. L.; Turner, Anthony P. F. (1984). "Ferrocene-mediated enzyme electrode for amperometric determination of glucose". Analytical Chemistry. 56: 667–671. doi:10.1021/ac00268a018. PMID 6721151.CS1 maint: uses authors parameter (link)
  2. Rausch, Marvin D.; Siegel, Armand (1968). "Organometallic π-complexes. XIV. Vinylmetallocenes". Journal of Organometallic Chemistry. 11: 317–324. doi:10.1016/0022-328X(68)80054-3.CS1 maint: uses authors parameter (link)
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