Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1328508 | Journal of Organometallic Chemistry | 2006 | 7 Pages |
A photochemical study of allyl iron complexes of the type, (η3-2-R-C3H4)Fe(CO)(NO)(X) (R = H or Cl; X = CO or PPh3) is presented. These compounds were studied in solid matrixes at 20 K, and at room temperature, by a combination of laser flash at 355 nm and steady-state photolysis. The predominant photochemical process for these compounds is loss of a CO ligand. In addition, exhaustive irradiation of (η3-2-R-C3H4)Fe(CO)(NO)(PPh3) with λexc > 300 nm provided evidence for a haptotropic shift of the allyl group from η3 to η1 coordination.
Graphical abstractA study of allyl iron complexes of the type, (η3-2-R-C3H4)Fe(CO)(NO)(X) (R = H or Cl; X = CO or PPh3) revels that the predominant photochemical process is loss of a CO ligand. UV irradiation of (η3-2-R-C3H4)Fe(CO)(NO)(PPh3) induced a haptotropic shift of the allyl group from η3 to η1 coordination.Figure optionsDownload full-size imageDownload as PowerPoint slide