E. Monflier et al., HIGHLY EFFICIENT TELOMERIZATION OF BUTADIENE INTO OCTADIENOL IN A MICELLAR SYSTEM - A JUDICIOUS CHOICE OF THE PHOSPHINE SURFACTANT COMBINATION/, Applied catalysis. A, General, 131(1), 1995, pp. 167-178
Telomerization of butadiene into octadienols in a micellar system and
in the presence of hydrophilic or hydrophobic phosphines derived from
triphenylphosphine has been investigated. Activities and selectivities
were strongly dependent on the steric properties of the phosphine and
on the nature of the surfactant/phosphine couple. The best results ha
ve been obtained with the water-soluble phosphine/cationic surfactant
combinations (octadienols selectivities > 70% and turnover frequencies
up to 830 h(-1)). The phosphine/anionic surfactant couples gave rise
to octadienols in poor selectivities (40%) and activities (100 h(-1)).
With the phosphine/neutral surfactant combinations, the results are s
trongly dependent on the nature of the phosphine. These results are in
terpreted from electrostatic interactions at the micelle-water interfa
ces.