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Gold(I) complexes with 'normal' 1,2,3-triazolylidene ligands: Synthesis and catalytic properties

机译:具有“正常” 1,2,3-三唑亚基配体的金(I)配合物:合成和催化性能

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摘要

1,2,3-Triazolylidenes as versatile, strong donor ligands have currently experienced a boost in complex synthesis as well as catalytic applications. Although many examples of "abnormal" 1,2,3-triazolylidenes have been described, their "normal" congeners have been barely examined to date (for abnormal carbenes the resonance structures of the carbenes cannot be drawn without adding additional charges, but this is possible for normal carbenes). Furthermore, no instance of utilization of this new ligand class in homogeneous catalysis can be found. Therefore, this work presents a variety of potential precatalysts descending from "normal" 1,2,3-triazolylidene Au chloride complexes. Synthesis and thorough characterization of the new compounds are presented, together with special ligand features such as buried volume and suspected anagostic interactions. The activity of the isolated precatalysts is examined in the intramolecular hydroamination of alkynes and compared with that of a popular imidazolylidene system. It is found that the activity of the best-performing "normal" 1,2,3-triazolylidene systems is quite similar to that of the imidazolylidene systems. However, mercury drop poisoning experiments suggest that improvements in ligand design are required to enhance catalyst stability.
机译:1,2,3-三唑基亚胺作为通用的强供体配体目前在复杂的合成以及催化应用中得到了发展。尽管已描述了许多“异常”的1,2,3-三唑基亚基的实例,但迄今为止,尚未对其“正常”同类物进行过检查(对于异常的卡宾,在不添加额外电荷的情况下无法得出卡宾的共振结构,但这是普通卡宾可以使用)。此外,没有发现在均相催化中利用这种新的配体类别的实例。因此,这项工作提出了从“正常的” 1,2,3-三唑基亚金氯化物络合物衍生的各种潜在的预催化剂。介绍了新化合物的合成和全面表征,以及特殊的配体特征,例如埋藏量和可疑的无声相互作用。在炔烃的分子内加氢胺化中检查了分离的前催化剂的活性,并将其与流行的咪唑基亚烷基体系的活性进行了比较。发现性能最佳的“正常” 1,2,3-三唑基亚烷基体系的活性与咪唑基亚烷基体系的活性非常相似。但是,汞滴中毒实验表明需要改进配体设计以增强催化剂的稳定性。

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