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Selective oxidation of silanes into silanols with water using [MnBr(CO)5] as a precatalyst
Authors:Emanuele Antico,Markus Leutzsch,Niklas Wessel,Thomas Weyhermü  ller,Christophe Werlé  ,Walter Leitner
Affiliation:Max Planck Institute for Chemical Energy Conversion, Stiftstr. 34–36, 45470 Mülheim an der Ruhr Germany.; Institut für Technische und Makromolekulare Chemie (ITMC), RWTH Aachen University, Worringer Weg 2, 52074 Aachen Germany ; Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr Germany ; Ruhr University Bochum, Universitätsstr. 150, 44801 Bochum Germany
Abstract:The development of earth-abundant catalysts for the selective conversion of silanes to silanols with water as an oxidant generating valuable hydrogen as the only by-product continues to be a challenge. Here, we demonstrate that [MnBr(CO)5] is a highly active precatalyst for this reaction, operating under neutral conditions and avoiding the undesired formation of siloxanes. As a result, a broad substrate scope, including primary and secondary silanes, could be converted to the desired products. The turnover performances of the catalyst were also examined, yielding a maximum TOF of 4088 h−1. New light was shed on the debated mechanism of the interaction between [MnBr(CO)5] and Si–H bonds based on the reaction kinetics (including KIEs of PhMe2SiD and D2O) and spectroscopic techniques (FT-IR, GC-TCD, 1H-, 29Si-, and 13C-NMR). The initial activation of [MnBr(CO)5] was found to result from the formation of a manganese(i) hydride species and R3SiBr, and the experimental data are most consistent with a catalytic cycle comprising a cationic tricarbonyl Mn(i) unit as the active framework.

This study presents the use of MnBr(CO)5 for the selective conversion of silanes to silanols with water as an oxidant generating valuable hydrogen as the only by-product.
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