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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >The copper-free Sonogashira cross-coupling reaction promoted by palladium complexes of nitrogen-containing chelating ligands in neat water at room temperature
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The copper-free Sonogashira cross-coupling reaction promoted by palladium complexes of nitrogen-containing chelating ligands in neat water at room temperature

机译:室温下净水中含氮螯合配体的钯配合物促进无铜Sonogashira交叉偶联反应

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摘要

The commercially available 2,2'-dipyridylamine was used as a supporting ligand in the palladium-catalyzed Sonogashira cross-coupling reaction. The reactions between aryl iodides and terminal alkynes with different steric hindrance can be efficiently performed in the absence of copper in neat water at room temperature. The superior catalytic performance of the catalytic system was attributed to water solubility of the palladium 2,2'-dipyridylamine complex. Palladium nanoparticles with small size and narrow size distribution were formed after the cross-coupling reaction.
机译:在钯催化的Sonogashira交叉偶联反应中,使用市售的2,2'-联吡啶胺作为支撑配体。在室温下在纯净水中不存在铜的情况下,可以有效地进行芳基碘化物和具有不同空间位阻的末端炔烃之间的反应。催化体系的优异催化性能归因于钯2,2'-二吡啶胺配合物的水溶性。在交叉偶联反应后,形成了具有小尺寸和窄尺寸分布的钯纳米颗粒。

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