Highly active palladium catalysts containing a 1,10-phenanthroline analogue N-heterocyclic carbene for room temperature Suzuki-Miyaura coupling reactions of aryl chlorides with arylboronic acids in aqueous media

Highly active palladium catalysts containing a 1,10-phenanthroline analogue N-heterocyclic carbene for room temperature Suzuki-Miyaura coupling reactions of aryl chlorides with arylboronic acids in aqueous media
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含有 1,10-菲咯啉类似物 N-杂环卡宾的高活性钯催化剂,用于水介质中芳基氯与芳基硼酸的室温 Suzuki-Miyaura 偶联反应

DOI:
10.1016/j.tetlet.2016.12.071
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发表时间:
2017-02
影响因子:
1.8
通讯作者:
Wang Jianhui
Wang Jianhui
中科院分区:
化学4区
文献类型:
--
作者:
Liu Guiyan;Liu Chengxin;Han Fangwai;Wang Zhongliang;Wang Jianhui

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合成了两个新的含1,10-邻菲罗啉类似物n -杂环卡宾(NHC)的钯(II)配合物。通过1H、13C NMR和元素分析对配合物进行了表征,并通过单晶x射线衍射对其结构进行了表征。以nhc -钯配合物为催化剂,在室温条件下进行了芳氯与芳硼酸的Suzuki-Miyaura偶联反应。在低催化剂负载下,交叉偶联反应效率高
Two new palladium (II) complexes containing a 1,10-phenanthroline analogue N-heterocyclic carbene (NHC) have been synthesized. The complexes were characterized by 1H and 13C NMR spectroscopy and elemental analysis and their structures were determined by single-crystal X-ray diffraction. The NHC-palladium complexes were employed as catalysts for Suzuki-Miyaura coupling reactions of aryl chlorides with arylboronic acids in aqueous media at room temperature. The cross-coupling reactions were highly efficient with low catalysts loadings
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