Studies of β-Diketone Complexes of Rhenium. VIII. The Reaction of β-Diketones with Chloropentacarbonylrhenium(I), and the Preparation of Complexes of the Type Re(CO)<sub>4</sub>(dik), Re<sub>2</sub>(CO)<sub>6</sub>(dik)<sub>2</sub>, Re<sub>2</sub>(CO)<sub>6</sub>Cl<sub>2</sub>(dikH)<sub>2</sub>, Re(CO)<sub>3</sub>L(dik), and Re(CO)<sub>2</sub>(dik)L<sub>2</sub>

Maurice Conrad Fredette, C. J. L. Lock

Canadian Journal of Chemistry · 1975 · 14 citations · 0 references

Concepts

Abstract

The reaction of β-diketones with Re(CO) 5 Cl gave compounds of stoichiometries Re 2 (CO) 6 dik 2 or Re 2 Cl 2 (CO) 6 (dikH) 2 . Reaction of the former compounds with carbon monoxide at high pressure gave Re(CO)4.dik, while with donor ligands such as pyridine or triphenylphosphine they gave compounds of stoichiometry Re(CO) 3 dikL. With triphenylphosphine further reaction gave Re(CO) 2 dik[P(C 6 H 5 ) 3 ] 2 . Compounds were investigated by infrared spectroscopy and mass spectroscopy, and a Cotton–Kraihânzel analysis was made of the carbonyl vibrational spectra in order to get an estimate of the π-acceptor ability of the β-ketoenolate ligands.