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

被引:12
作者
Antico, Emanuele [1 ,2 ]
Leutzsch, Markus [3 ]
Wessel, Niklas [1 ,2 ]
Weyhermueller, Thomas [1 ]
Werle, Christophe [1 ,4 ]
Leitner, Walter [1 ,2 ]
机构
[1] Max Planck Inst Chem Energy Convers, Stiftstr 34-36, D-45470 Mulheim, Germany
[2] Rhein Westfal TH Aachen, Inst Tech & Makromol Chem ITMC, Worringer Weg 2, D-52074 Aachen, Germany
[3] Max Planck Inst Kohlenforsch, Kaiser Wilhelm Pl 1, D-45470 Mulheim, Germany
[4] Ruhr Univ Bochum, Univ Str 150, D-44801 Bochum, Germany
关键词
HYDROLYTIC OXIDATION; CATALYZED OXIDATION; HYDROGEN-PRODUCTION; BOND ACTIVATION; SILICON ANALOG; ORGANOSILANES; EFFICIENT; HYDROSILANES; COMPLEX; CARBON;
D O I
10.1039/d2sc05959b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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, H-1-, Si-29-, and C-13-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.
引用
收藏
页码:54 / 60
页数:8
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