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Palladium(II) complexes containing sterically bulky O, N donor ligands: Synthesis, characterization and catalytic activity in the Suzuki-Miyaura and Sonogashira coupling reactions
Journal of Organometallic Chemistry ( IF 2.3 ) Pub Date : 2019-12-18 , DOI: 10.1016/j.jorganchem.2019.121080
Raja Nandhini , Paranthaman Vijayan , Galmari Venkatachalam

A new class of palladium(II)1-(arylazo)naphtholate complexes of the type [Pd(L1-4)2] containing sterically bulky O, N donor functionalized arylazo ligands has been synthesized. These palladium(II) complexes were characterized by elemental analysis and spectral (FT-IR, UV–Vis, 1H NMR and 13C NMR) studies. The molecular structure of the Palladium(II) complexes [Pd(L1)2] and [Pd(L2)2] were established by X-ray crystallography. These complexes were found to efficiently catalyze the Suzuki-Miyaura coupling of arylboronic acids and aryl halides, and the Sonogashira reaction of aryl halides and phenylacetylene in DMF and i-PrOH media to afford the corresponding C–C coupling products in high yields.



中文翻译:

含有体积庞大的O,N供体配体的钯(II)配合物:Suzuki-Miyaura和Sonogashira偶联反应的合成,表征和催化活性

合成了新型的[Pd(L 1-42 ]型钯(II)1-(芳基偶氮)萘甲酸酯络合物,其含有空间庞大的O,N供体官能化的芳基偶氮配体。这些钯(II)配合物的特征在于元素分析和光谱(FT-IR,UV-Vis,1 H NMR和13 C NMR)研究。通过X射线晶体学确定钯(II)配合物[Pd(L 12 ]和[Pd(L 22 ]的分子结构。发现这些络合物可有效催化DMF和i中芳基硼酸和芳基卤化物的Suzuki-Miyaura偶联以及芳基卤化物和苯乙炔的Sonogashira反应。-PrOH介质可提供高收率的相应C–C偶联产物。

更新日期:2019-12-18
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