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.
| Original language | English |
|---|---|
| Pages (from-to) | 337-344 |
| Number of pages | 8 |
| Journal | Canadian Journal of Chemistry |
| Volume | 84 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Feb 2006 |
| Externally published | Yes |
Keywords
- Acetyl and acetate complexes
- Alkynols
- Allenyl iron complexes
- CO and methanol activation
- Crystal structure
- Iron carbonyls
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