Ionic liquids in regioselective platinum-catalysed hydroformylation

Citation
P. Wasserscheid et H. Waffenschmidt, Ionic liquids in regioselective platinum-catalysed hydroformylation, J MOL CAT A, 164(1-2), 2000, pp. 61-67
Citations number
24
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
ISSN journal
13811169 → ACNP
Volume
164
Issue
1-2
Year of publication
2000
Pages
61 - 67
Database
ISI
SICI code
1381-1169(200012)164:1-2<61:ILIRPH>2.0.ZU;2-T
Abstract
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.