Abstract
Aminoferrocene has been converted into formamidoferrocene, which exists in solution as an equilibrium mixture of two rotational isomers, a monometic cis form and a dimeric (or oligomeric) trans form. Variable-temperature 2H and 13C1H NMR spectra have been used to measure AG 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.
| Original language | English |
|---|---|
| Pages (from-to) | 301-306 |
| Number of pages | 6 |
| Journal | Organometallics |
| Volume | 9 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 1 Feb 1990 |
Keywords
- aminoferrocene
- formamidoferrocene
- isocyanoferrocene
- isothiocyanatoferrocene
Fingerprint
Dive into the research topics of 'Ferrocene derivatives. 23. Isocyanoferrocene and isothiocyanatoferrocene'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver