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Updated: Aug 15, 2025

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
Published on: October 18, 2019
Selective oxidation of silanes into silanols with water using [MnBr(CO)5] as a precatalyst
Emanuele Antico1,2, Markus Leutzsch3, Niklas Wessel1,2
1Max Planck Institute for Chemical Energy Conversion Stiftstr. 34-36 45470 Mülheim an der Ruhr Germany christophe.werle@cec.mpg.de walter.leitner@cec.mpg.de.
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.
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