New and Selective Routes to Functionalized Biferrocenes and Terferrocenes by [3 + 2] Cycloadditions of Alkynes with Bridging C3 Ligands in Diiron Complexes
| Autor: | Mauro Salmi, Valerio Zanotti, Rita Mazzoni, Luigi Busetto, Stefano Zacchini |
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| Přispěvatelé: | M. Salmi, L. Busetto, R. Mazzoni, S. Zacchini, V. Zanotti |
| Rok vydání: | 2011 |
| Předmět: | |
| Zdroj: | Organometallics. 30:1175-1181 |
| ISSN: | 1520-6041 0276-7333 |
| DOI: | 10.1021/om101162r |
| Popis: | The diiron bridging enaminoalkylidene complex [Fe2{μ-η1:η3-C(Fc)CHCH(NMe2)}(μ-CO)(CO)- (Cp)2] (2), containing a ferrocenyl group on the bridging ligand, reacts with HC≡CR, affording the corresponding 3-R-substituted 1,100-biferrocene (R =CPh2OH, 4a; R = Tol, 4b; R = CO2Me, 4c; R = CH2OH, 4d). In a related reaction, the μ-vinylaminoalkylidene complex [Fe2{μ-η1:η3-C- (NMe2)CHCH(CO2Me)}(μ-CO)(CO)(Cp)2] (1a), upon treatment with ethynylferrocene, leads to the formation of 2-NMe2-4-CO2Me-1,100-biferrocene (4f). Conversely, the μ-enaminoalkylidene complex [Fe2{μ-η1:η3-C(Tol)CHCH(NMe2)}(μ-CO)(CO)(Cp)2] (1b) reacts with ethynylferrocene, affording a mixture of monosubstituted biferrocene 4b and disubstituted 2-NMe2-4-Tol-1,100- biferrocene (4e), in comparable yields. Reaction of 2 with ethynylferrocene (HC≡CFc) leads to the formation of a mixture of 1,3-terferrocene (5a) and the 5-NMe2-substituted 1,3-terferrocene (5b). Investigation of the reactivity of the vinyliminium complex [Fe2{μ-η1:η3-C(Fc)CHCNMe2}(μ-CO)- (CO)(Cp)2][SO3CF3] (3) with HC≡CCPh2OH is also reported: the reaction affords selectively the 3-NMe2-4-R-disubstituted 1,100-biferrocene (6). The molecular structure of 5a has been determined by X-ray diffraction studies. |
| Databáze: | OpenAIRE |
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