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首页> 外文期刊>Turkish journal of chemistry >Palladium-catalysed Suzuki-Miyaura cross-coupling with imidazolylidene ligands substituted by crowded resorcinarenyl and calixarenyl units
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Palladium-catalysed Suzuki-Miyaura cross-coupling with imidazolylidene ligands substituted by crowded resorcinarenyl and calixarenyl units

机译:钯催化的Suzuki-Miyaura交叉偶联与被拥挤的间苯二甲烯基和杯芳烃基单元取代的咪唑基亚基配体

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摘要

Two N-heterocyclic carbene (NHC) palladium complexes of formula [PdBr2 (NHC)(pyridine)] in which the carbenic ring is flanked by sterically crowded cavitand substituents were prepared from appropriate imidazolium salts bearing either two resorcinarene or a combination of resorcinarene and calixarene fragments. Both complexes displayed high stability and good activities in the cross-coupling of aryl bromides with phenyl boronic acid. One of the imidazolium salts was characterised by an X-ray diffraction study.
机译:由式[PdBr 2(NHC)(吡啶)]构成的两个N-杂环卡宾(NHC)钯配合物,其中碳环被空间拥挤的cavitand取代基侧接,是由合适的咪唑鎓盐制备的,所述咪唑鎓盐带有两个间苯二芳烃或间苯二芳烃和杯芳烃的组合碎片。两种配合物在芳基溴化物与苯基硼酸的交叉偶联中均显示出高稳定性和良好的活性。咪唑鎓盐之一通过X射线衍射研究表征。

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