Reaction Mechanism of Pd-Catalyzed “CO-Free” Carbonylation Reaction Uncovered by In Situ Spectroscopy: The Formyl Mechanism
Geitner R, Gurinov A, Huang T, Kupfer S, Gräfe S, Weckhuysen BM (2021)
Publication Type: Journal article
Publication year: 2021
Journal
Book Volume: 60
Pages Range: 3422-3427
Journal Issue: 7
DOI: 10.1002/anie.202011152
Abstract
“CO-free” carbonylation reactions, where synthesis gas (CO/H2) is substituted by C1 surrogate molecules like formaldehyde or formic acid, have received widespread attention in homogeneous catalysis lately. Although a broad range of organics is available via this method, still relatively little is known about the precise reaction mechanism. In this work, we used in situ nuclear magnetic resonance (NMR) spectroscopy to unravel the mechanism of the alkoxycarbonylation of alkenes using different surrogate molecules. In contrast to previous hypotheses no carbon monoxide could be found during the reaction. Instead the reaction proceeds via the C−H activation of in situ generated methyl formate. On the basis of quantitative NMR experiments, a kinetic model involving all major intermediates is built which enables the knowledge-driven optimization of the reaction. Finally, a new reaction mechanism is proposed on the basis of in situ observed Pd-hydride, Pd-formyl and Pd-acyl species.
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How to cite
APA:
Geitner, R., Gurinov, A., Huang, T., Kupfer, S., Gräfe, S., & Weckhuysen, B.M. (2021). Reaction Mechanism of Pd-Catalyzed “CO-Free” Carbonylation Reaction Uncovered by In Situ Spectroscopy: The Formyl Mechanism. Angewandte Chemie International Edition, 60(7), 3422-3427. https://doi.org/10.1002/anie.202011152
MLA:
Geitner, Robert, et al. "Reaction Mechanism of Pd-Catalyzed “CO-Free” Carbonylation Reaction Uncovered by In Situ Spectroscopy: The Formyl Mechanism." Angewandte Chemie International Edition 60.7 (2021): 3422-3427.
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