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首页> 外文期刊>Journal of Inclusion Phenomena and Macrocyclic Chemistry >Palladium complexes of o-xylylene-linked alkoxybenzimidazolin-2-ylidenes containing aryl N-substituents: examples of C-H activation and the formation of a tri-nuclear palladium complex
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Palladium complexes of o-xylylene-linked alkoxybenzimidazolin-2-ylidenes containing aryl N-substituents: examples of C-H activation and the formation of a tri-nuclear palladium complex

机译:含芳基N取代基的邻二甲苯基连接的烷氧基苯并咪唑啉-2-亚烷基的钯配合物:C-H活化和三核钯配合物形成的实例

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摘要

Palladium complexes of new bidentate N-heterocyclic carbene (NHC) incorporating benzimidazolin-2-ylidene units have been synthesized and structurally and spectroscopically characterised. The NHC ligands are furnished with aryl substituents on the nitrogen atoms and electron-donating butoxy groups on the benzo-fused ring. The incorporation of these aryl substituents on the bis(NHC) ligands leads to interesting and unexpected conformations around the palladium atoms, and interesting reactivity, including cyclometallation and the formation of a tri-nuclear species. One of the complexes has been studied in an initial series of Mizoroki-Heck and Suzuki-Miyaura cross-coupling reactions but shows moderate to poor activity.
机译:结合苯并咪唑啉-2-亚烷基单元的新的双齿N-杂环卡宾(NHC)的钯配合物已经合成,结构和光谱表征。 NHC配体在氮原子上具有芳基取代基,并在苯并稠合环上具有供电子性丁氧基。这些芳基取代基在双(NHC)配体上的掺入会导致钯原子周围有趣的和意想不到的构象,以及有趣的反应性,包括环金属化和三核物种的形成。已在Mizoroki-Heck和Suzuki-Miyaura交叉偶联反应的初始系列中研究了一种配合物,但显示出中等至较差的活性。

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