Hydrosilylation of C−C Multiple Bonds Using (Me3Si)3SiH in Water. Comparative Study of the Radical Initiation Step
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 organic solvent-soluble and water-soluble substrates. Different initiation methods to accomplish the radical-indu...
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Autores principales: | , , , , |
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Formato: | Artículo |
Lenguaje: | Inglés |
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Universidad de Belgrano - Facultad de Ciencias Exactas y Naturales - Proyectos de Investigación
2014
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Materias: | |
Acceso en línea: | http://repositorio.ub.edu.ar/handle/123456789/2726 |
Aporte de: |
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I36-R142-123456789-2726 |
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record_format |
dspace |
institution |
Universidad de Belgrano |
institution_str |
I-36 |
repository_str |
R-142 |
collection |
Repositorio Institucional - Universidad de Belgrano (UB) |
language |
Inglés |
topic |
Hydrosilylation Multiple Bonds Radical Initiation Step hidrosililación Iniciación por radicales Paso Enlaces múltiples |
spellingShingle |
Hydrosilylation Multiple Bonds Radical Initiation Step hidrosililación Iniciación por radicales Paso Enlaces múltiples Postigo, Al Kopsov, Sergey Zlotsky, Simon S. Ferreri, Carla Chatgilialoglu, Chryssostomos Hydrosilylation of C−C Multiple Bonds Using (Me3Si)3SiH in Water. Comparative Study of the Radical Initiation Step |
topic_facet |
Hydrosilylation Multiple Bonds Radical Initiation Step hidrosililación Iniciación por radicales Paso Enlaces múltiples |
description |
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 organic solvent-soluble and water-soluble substrates. Different initiation methods to accomplish the radical-induced hydrosilylation reaction of C−C multiple bonds in water with (Me3Si)3SiH are presented. In the thermal decomposition of azo compounds, the system comprising substrate, silane, and azo-initiator (ACCN) mixed in aqueous medium at 100 °C worked well for both hydrophilic and hydrophobic substrates, with the only variation that the amphiphilic thiol HOCH2CH2SH was also needed in the case of the water-soluble compounds. |
format |
Article |
author |
Postigo, Al Kopsov, Sergey Zlotsky, Simon S. Ferreri, Carla Chatgilialoglu, Chryssostomos |
author_facet |
Postigo, Al Kopsov, Sergey Zlotsky, Simon S. Ferreri, Carla Chatgilialoglu, Chryssostomos |
author_sort |
Postigo, Al |
title |
Hydrosilylation of C−C Multiple Bonds Using (Me3Si)3SiH in Water. Comparative Study of the Radical Initiation Step |
title_short |
Hydrosilylation of C−C Multiple Bonds Using (Me3Si)3SiH in Water. Comparative Study of the Radical Initiation Step |
title_full |
Hydrosilylation of C−C Multiple Bonds Using (Me3Si)3SiH in Water. Comparative Study of the Radical Initiation Step |
title_fullStr |
Hydrosilylation of C−C Multiple Bonds Using (Me3Si)3SiH in Water. Comparative Study of the Radical Initiation Step |
title_full_unstemmed |
Hydrosilylation of C−C Multiple Bonds Using (Me3Si)3SiH in Water. Comparative Study of the Radical Initiation Step |
title_sort |
hydrosilylation of c−c multiple bonds using (me3si)3sih in water. comparative study of the radical initiation step |
publisher |
Universidad de Belgrano - Facultad de Ciencias Exactas y Naturales - Proyectos de Investigación |
publishDate |
2014 |
url |
http://repositorio.ub.edu.ar/handle/123456789/2726 |
work_keys_str_mv |
AT postigoal hydrosilylationofccmultiplebondsusingme3si3sihinwatercomparativestudyoftheradicalinitiationstep AT kopsovsergey hydrosilylationofccmultiplebondsusingme3si3sihinwatercomparativestudyoftheradicalinitiationstep AT zlotskysimons hydrosilylationofccmultiplebondsusingme3si3sihinwatercomparativestudyoftheradicalinitiationstep AT ferrericarla hydrosilylationofccmultiplebondsusingme3si3sihinwatercomparativestudyoftheradicalinitiationstep AT chatgilialogluchryssostomos hydrosilylationofccmultiplebondsusingme3si3sihinwatercomparativestudyoftheradicalinitiationstep |
bdutipo_str |
Repositorios |
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1764820529249779713 |