Counterion effect in cobaltate-catalyzed alkene hydrogenation
Gawron, Martin and Gilch, Franziska and Schmidhuber, Daniel and Kelly, John A. and Horsley Downie, Thomas M. and Jacobi von Wangelin, Axel and Rehbein, Julia and Wolf, Robert (2024) Counterion effect in cobaltate-catalyzed alkene hydrogenation. Angewandte Chemie International Edition, 63 (6). e202315381. ISSN 1521-3773 (https://doi.org/10.1002/anie.202315381)
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Abstract
We show that countercations exert a remarkable influence on the ability of anionic cobaltate salts to catalyze challenging alkene hydrogenations. An evaluation of the catalytic properties of [Cat][Co(?4-cod)2] (Cat=K (1), Na (2), Li (3), (Depnacnac)Mg (4), and N(nBu)4 (5); cod=1,5-cyclooctadiene, Depnacnac={2,6-Et2C6H3NC(CH3)}2CH)]) demonstrated that the lithium salt 3 and magnesium salt 4 drastically outperform the other catalysts. Complex 4 was the most active catalyst, which readily promotes the hydrogenation of highly congested alkenes under mild conditions. A plausible catalytic mechanism is proposed based on density functional theory (DFT) investigations. Furthermore, combined molecular dynamics (MD) simulation and DFT studies were used to examine the turnover-limiting migratory insertion step. The results of these studies suggest an active co-catalytic role of the counterion in the hydrogenation reaction through the coordination to cobalt hydride intermediates.
ORCID iDs
Gawron, Martin, Gilch, Franziska, Schmidhuber, Daniel, Kelly, John A., Horsley Downie, Thomas M. ORCID: https://orcid.org/0000-0001-5027-450X, Jacobi von Wangelin, Axel, Rehbein, Julia and Wolf, Robert;-
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Item type: Article ID code: 89520 Dates: DateEvent5 February 2024Published4 January 2024Published Online7 December 2023AcceptedSubjects: Science > Chemistry Department: Faculty of Science > Pure and Applied Chemistry Depositing user: Pure Administrator Date deposited: 07 Jun 2024 16:54 Last modified: 12 Dec 2024 15:30 URI: https://strathprints.strath.ac.uk/id/eprint/89520