Full Paper
Hydrocarboxylation of Terminal Alkenes in Supercritical Carbon Dioxide
Article first published online: 4 JUL 2008
DOI: 10.1002/ejic.200800282
Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Tortosa Estorach, C., Orejón, A., Ruiz, N., Masdeu-Bultó, A. M. and Laurenczy, G. (2008), Hydrocarboxylation of Terminal Alkenes in Supercritical Carbon Dioxide. European Journal of Inorganic Chemistry, 2008: 3524–3531. doi: 10.1002/ejic.200800282
Publication History
- Issue published online: 17 JUL 2008
- Article first published online: 4 JUL 2008
- Manuscript Received: 18 MAR 2008
Funded by
- Generalitat de Catalunya. Grant Number: 2005SGR00777
- Ministerio de Educacion y Ciencia (MEC). Grant Numbers: CTQ2004-03831/PPQ, CSD2006-0003
- Swiss State Secretariat for Education and Research. Grant Numbers: SER C03.0020, COST D30 Action
- European Science Foundation
Keywords:
- Hydrocarboxylation;
- Hydroxycarbonylation;
- Palladium;
- Supercritical fluids
Graphical Abstract

The catalytic hydrocarboxylation of linear alkenes to carboxylic acids using supercritical carbon dioxide as a solvent was studied. High selectivities in acids have been obtained when adding a perfluorinated surfactant to the reaction mixture. Multinuclear high-pressure NMR spectroscopic studies in [D8]THF and in supercritical CO2 show the formation of Pd0 species.
Abstract
The catalytic hydrocarboxylation of linear alkenes to carboxylic acids using supercritical carbon dioxide as a solvent was studied. High selectivities in acids have been obtained. The best results were achieved when adding a perfluorinated surfactant to the reaction mixture (93 % conversions and ca. 80 % selectivity). Comparative multinuclear high-pressure NMR spectroscopic studies in [D8]THF and in supercritical CO2 show the formation of Pd0 species. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)

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