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用于硅氢键活化的含氮路易斯酸的受阻路易斯酸碱对

Frustrated Lewis Pairs Comprising Nitrogen Lewis Acids for Si-H Bond Activation.

作者信息

Avigdori Idan, Pogoreltsev Alla, Kaushanski Alexander, Fridman Natalia, Gandelman Mark

机构信息

Schulich Faculty of Chemistry, Technion-Israel Institute of Technology, Technion City, Haifa, 32000, Israel.

出版信息

Angew Chem Int Ed Engl. 2020 Dec 21;59(52):23476-23479. doi: 10.1002/anie.202008798. Epub 2020 Oct 15.

Abstract

N-heterocyclic nitrogen Lewis acids are a recent addition to the field of organic chemistry. Based on nitrenium cations, these acids where previously shown to generate Lewis adducts when combined with the appropriate Lewis bases. Herein, a triazinium-based Lewis acid was combined with tBuP to generate a frustrated Lewis pair (FLP) capable of cleaving, for the first time, Si-H bonds in silanes. Whereas low yields were initially encountered owing to insufficient Lewis acidity, a new nitrenium-based Lewis acid was synthesized, and its superior Lewis acidity was experimentally and computationally confirmed. A FLP based on this acid cleaved the Si-H bond in PhSiH, generating the triazane product in a quantitative yield. This unprecedented N-H triazane was fully characterized by multinuclear NMR techniques and single-crystal X-ray crystallography. A new class of compounds, N-H triazanes display the potential capacity to participate in hydride transfer reactions.

摘要

N-杂环氮路易斯酸是有机化学领域的新成员。基于氮鎓阳离子,这些酸先前已表明与适当的路易斯碱结合时会生成路易斯加合物。在此,一种基于三嗪鎓的路易斯酸与tBuP结合,首次生成了能够裂解硅烷中Si-H键的受阻路易斯对(FLP)。由于路易斯酸性不足,最初产率较低,因此合成了一种新的基于氮鎓的路易斯酸,并通过实验和计算证实了其优越的路易斯酸性。基于这种酸的FLP裂解了PhSiH中的Si-H键,以定量产率生成了三氮烷产物。这种前所未有的N-H三氮烷通过多核NMR技术和单晶X射线晶体学进行了全面表征。作为一类新的化合物,N-H三氮烷显示出参与氢化物转移反应的潜在能力。

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