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首页> 外文期刊>Organometallics >Formation and Role of Palladium Chalcogenide and Other Species in Suzuki?Miyaura and Heck C?C Coupling Reactions Catalyzed with Palladium(II) Complexes of Organochalcogen Ligands: Realities and Speculations
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Formation and Role of Palladium Chalcogenide and Other Species in Suzuki?Miyaura and Heck C?C Coupling Reactions Catalyzed with Palladium(II) Complexes of Organochalcogen Ligands: Realities and Speculations

机译:有机碳素配体的钯(II)配合物催化的Suzuki?Miyaura和Heck C?C偶联反应中硫属硫化物和其他物种的形成和作用:现实与推测

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Palladium(II) complexes of organochalcogen ligands have emerged as viable alternatives to complexes of phosphine/carbene ligands for Suzuki?Miyaura and Heck C?C cross coupling reactions, as thermal stability and air and moisture sensitivity are not impediments with many of them. Sometimes they outperform their phosphorus analogues. The ease in handling and synthesis of palladium(II) complexes of organochalcogen ligands has made them attractive. For such complexes in situ generation of palladium containing nanoparticles (NPs) or palladium(0) species and their role in catalysis have been reported. However, in a large number of reports such species are ill defined or speculated, particularly due to limited experimental investigations. Recently in some cases in situ generated palladium species have been studied in detail to establish their identities, which appear to be palladium chalcogenides phases or Pd(0) protected with organochalcogen fragments. In this review the current status regarding in situ generated such species is summarized and critically analyzed to demarcate realities from speculative propositions.
机译:有机硫属元素配体的钯(II)配合物已成为铃木?宫浦和Heck C?C交叉偶联反应的膦/卡宾配体的配合物的可行替代品,因为热稳定性,空气和湿气敏感性对许多都没有阻碍。有时它们的表现优于磷类似物。有机硫属元素配体的钯(II)配合物的易于处理和合成使其具有吸引力。对于这样的络合物,已经报道了含钯的纳米颗粒(NP)或钯(0)物质的原位生成及其在催化中的作用。但是,在许多报道中,这类物种的定义或推测不明确,特别是由于有限的实验研究。最近,在某些情况下,对原位生成的钯物种进行了详细研究,以建立其身份,这些身份似乎是钯硫属元素化物相或有机硫属元素片段保护的Pd(0)。在这篇综述中,总结并严格分析了有关就地产生的此类物种的当前状况,以将现实与投机命题区分开来。

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