The regioselective, platinum-catalysed hydroformylation of functionalized a
nd non-functionalized olefins was chosen to demonstrate the great potential
of room temperature liquid chlorostannate ionic liquids as solvents for ho
mogeneous catalysis. The moderate Lewis-acidity of these ionic liquids allo
ws the activation of the Pt-catalyst combined with tolerance of the functio
nal groups in the substrate. Dissolved in chlorostannate ionic liquids, the
Pt-catalyst shows enhanced stability and selectivity in the hydroformylati
on of methyl-3-pentenoate (M3P) compared to the identical reaction in conve
ntional organic solvents. In the case of 1-octene hydroformylation, a bipha
sic reaction system could be realised using the chlorostannate ionic liquid
s as catalyst solvents. Besides the catalytic results, a method to determin
e the Lewis-acidity of chlorostannate ionic liquids by Sn-119 NMR is presen
ted. (C) 2000 Elsevier Science B.V. All rights reserved.