Abstract
The complex Fe2(CO)7(H2CCCH2) (1) is obtained starting from a variety of functionalized alkynes that can release C3 fragments during the reactions with Fe3(CO) 12 or Fe(CO)5 in CH3OH-KOH solutions. Owing to the oily nature of 1, it was reacted with triphenylphosphine, and the structure of the resulting title compound (1a) has been determined by X-ray analysis. Complex 1a shows a new coordination mode of a H2C=C=CH2 ligand to a diiron centre and is, to our knowledge, unprecedented. We have also found that 1 (and 1a) are by-products, and not intermediates in the formation of complex 3. A discussion of the possible reaction pathways is given.
Lingua originale | Inglese |
---|---|
pagine (da-a) | 337-344 |
Numero di pagine | 8 |
Rivista | Canadian Journal of Chemistry |
Volume | 84 |
Numero di pubblicazione | 2 |
DOI | |
Stato di pubblicazione | Pubblicato - feb 2006 |
Pubblicato esternamente | Sì |