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Selective oxidation of silanes into silanols with water using [MnBr(CO)5] as a precatalyst.


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.

SUBMITTER: Antico E 

PROVIDER: S-EPMC9769106 | biostudies-literature | 2022 Dec

REPOSITORIES: biostudies-literature

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Selective oxidation of silanes into silanols with water using [MnBr(CO)<sub>5</sub>] as a precatalyst.

Antico Emanuele E   Leutzsch Markus M   Wessel Niklas N   Weyhermüller Thomas T   Werlé Christophe C   Leitner Walter W  

Chemical science 20221201 1


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)<sub>5</sub>] 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  ...[more]

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