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Z. Naturforsch. 2012, 67b, 1061 – 1069
doi:10.5560/ZNB.2012-0157
Operando Infrared Spectroscopic and Quantum-chemical Studies on Iridium-catalyzed Hydroformylation
Dieter Hess1, Bernd Hannebauer2, Matthias König1, Matthias Reckers1, Stefan Buchholz1, and Robert Franke1,3
1 Evonik Industries AG, Paul-Baumann-Straße 1, 45772 Marl, Germany
2 AQura GmbH, Evonik Industries, Rodenbacher Chaussee 4, 63457 Hanau, Germany
3 Lehrstuhl für Theoretische Chemie, Ruhr-Universität Bochum, 44780 Bochum, Germany
Reprint requests to Prof. Dr. R. Franke. E-mail: robert.franke@evonik.com
Received June 8, 2012 / published online October 8, 2012
Dedicated to Professor Heribert Offermanns on the occasion of his 75th birthday
Hydroformylation of 1-butene using a triphenylphosphine-modified iridium catalyst was investigated by operando infrared spectroscopy. The spectra were interpreted by comparison with quantum-chemically calculated vibrational spectra at the density functional theory level. The processes during activation of the catalyst and hydroformylation were investigated in detail, and the results are discussed. The recently discovered phenomenon of activity enhancement in iridium-catalyzed hydroformylation by a preceding activation step, in which the reaction mixture is treated with synthesis gas containing an excess of carbon monoxide under pressure, could be correlated with the appearance of a complex HIr(PPh3)(CO)3. The similarities and differences between iridium- and rhodium-catalyzed hydroformylation are discussed.
Key words: Hydroformylation, Rhodium, Iridium, Triphenylphosphine, Operando Spectroscopy, Density Functional Theory
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