Английская Википедия:Biferrocene

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Версия от 05:22, 9 февраля 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{short description|Organometallic compound}} {{Chembox | ImageFile = Biferrocene.svg | ImageSize = 122 | ImageAlt = | IUPACName = 1,1"-Biferrocene | OtherNames = |Section1={{Chembox Identifiers | CASNo = 1287-38-3 | PubChem = 11984633 | ChemSpiderID = 10157133 | SMILES = C1=C[CH-]C=C1.[Fe+2].C2=C[C-](C=C2)[C-](C=C3)C=C3.[Fe+2].C1=C[CH-]C=C1 | StdInChI=1S/C10H8.2C5H5.2Fe/c1-2-6-9(5-1...»)
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Шаблон:Short description Шаблон:Chembox Biferrocene is the organometallic compound with the formula [(C5H5)Fe(C5H4)]2. It is the product of the formal dehydrocoupling of ferrocene, analogous the relationship between biphenyl and benzene. It is an orange, air-stable solid that is soluble in nonpolar organic solvents.

Biferrocene can be prepared by the Ullmann coupling of iodoferrocene.[1] Its one-electron oxidized derivative [(C5H5)Fe(C5H4)]2+ attracted attention as a prototypical mixed-valence compound.[2]

A related compound is biferrocenylene, [Fe(C5H4)2]2 wherein all cyclopentadienyl rings are coupled. Formally, biferrocene is derived from one fulvalene ligand, and biferrocenylene is derived from two.

Reactions

Biferrocene can easily be converted into a mixed-valence complex, which is called biferrocenium. This [Fe(II)-Fe(III)] cation is a class II type (0.707 > α > 0) mixed-valence complex according to the Robin-Day classification.[2]

Derivatives

Aminophosphine ligands with biferroceno substituents have been prepared as catalysts for asymmetric allylic substitution[3] and asymmetric hydrogenation of alkenes.[4]

Related compounds

References

Шаблон:Cyclopentadienide complexes

Шаблон:Inorganic-compound-stub