Affiliation:
1. Max Planck Institute for Chemical Energy Conversion Stiftstr. 34–36 45470 Mülheim Germany
2. Institut für Technische und Makromolekulare Chemie RWTH Aachen University Worringerweg 2 52074 Aachen Germany
3. Ruhr University Bochum Universitätsstr. 150 44801 Bochum Germany
Abstract
AbstractColloidal and supported manganese nanoparticles were synthesized following an organometallic approach and applied in the catalytic transfer hydrogenation (CTH) of aldehydes and ketones. Reaction parameters for the preparation of colloidal nanoparticles (NPs) were optimized to yield small (2–2.5 nm) and well‐dispersed NPs. Manganese NPs were further immobilized on an imidazolium‐based supported ionic phase (SILP) and characterized to evaluate NP size, metal loading, and oxidation states. Oxidation of the Mn NPs by the support was observed resulting in an average formal oxidation state of +2.5. The MnOx@SILP material showed promising performance in the CTH of aldehydes and ketones using 2‐propanol as a hydrogen donor, outperforming previously reported Mn NPs‐based CTH catalysts in terms of metal loading‐normalized turnover numbers. Interestingly, MnOx@SILP were found to lose activity upon air exposure, which correlates with an additional increase in the average oxidation state of Mn as revealed by X‐ray absorption spectroscopic studies.
Funder
Max-Planck-Gesellschaft
Deutsche Forschungsgemeinschaft
Alexander von Humboldt-Stiftung
Cited by
1 articles.
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