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Different radical initiation techniques of hydrosilylation reactions of multiple bonds in water: Thermal and photochemical initiation

机译:水中多个键的氢化硅烷化反应的不同自由基引发技术:热引发和光化学引发

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摘要

The classical radical-based hydrosilylation reaction of organic compounds bearing C-C multiple bonds is usually carried out in organic solvents and is herein presented in water with both hydrophobic and hydrophilic substrates. Thermal and photochemical initiations are used to accomplish the radical-induced hydrosilylation reaction of C-C multiple bonds in water with tris(trimethylsilyl)silane ((Me_3Si)_3SiH). Photochemical radical initiation in the absence of a chemical radical precursor other than the silane is found to be a very efficient and convenient method to induce the hydrosilylation reaction of C-C multiple bonds of organic compounds with (Me_3Si)_3SiH in water. This new alternate radical-based methodology studied in water is confronted with the classical radical thermal initiation of hydrosilylation reactions triggered through the thermal decomposition of azo compounds.
机译:具有C-C多个键的有机化合物的经典的基于自由基的氢化硅烷化反应通常在有机溶剂中进行,并且本文在具有疏水性和亲水性底物的水中呈现。使用热引发和光化学引发来完成水中的C-C多键与三(三甲基甲硅烷基)硅烷((Me_3Si)_3SiH)的自由基诱导的氢化硅烷化反应。发现在不存在除了硅烷以外的化学自由基前体的情况下的光化学自由基引发是诱导水中有机化合物与(Me_3Si)_3SiH的C-C多键的硅氢加成反应的非常有效和方便的方法。在水中研究的这种新的基于自由基的替代方法学面临着由偶氮化合物的热分解引发的氢化硅烷化反应的经典自由基热引发。

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