Ferrocene derivatives. 23. Isocyanoferrocene and isothiocyanatoferrocene
Aminoferrocene has been converted into formamidoferrocene, which exists in solution as an equilibrium mixture of two rotational isomers, a monomeric cis form and a dimeric (or oligomeric) transform. Variable-temperature {sup 1}H and {sup 13}C({sup 1}H) NMR spectra have been used to measure {Delta}G{...
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Veröffentlicht in: | Organometallics 1990-02, Vol.9 (2), p.301-306 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Aminoferrocene has been converted into formamidoferrocene, which exists in solution as an equilibrium mixture of two rotational isomers, a monomeric cis form and a dimeric (or oligomeric) transform. Variable-temperature {sup 1}H and {sup 13}C({sup 1}H) NMR spectra have been used to measure {Delta}G{double dagger} for the hindered internal rotation about the C-N bond. Dehydration of formamidoferrocene yields isocyanoferrocene, which has been characterized by complex formation with iron and molybdenum carbonyls. A high-yield conversion of aminoferrocene into isothiocyanatoferrocene is described. |
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ISSN: | 0276-7333 1520-6041 |
DOI: | 10.1021/om00116a002 |