Angewandte Chemie International Edition · 2020 · 43 citations · 29 references
Natural SciencesChemistryComputational ChemistryOrganic ChemistryTheoretical ChemistryAcid-base ChemistryChemical BondingCoordination ChemistryCrystal ChemistryHeterocyclic ChemistryHeterocyclic CompoundsFrustrated Lewis PairsHeterocyclic ReactivityHydride Transfer ChemistryHydride Transfer ProcessesLewis AcidityLewis StructuresOrganic Chemistry InstructionSilane Coupling
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 t Bu 3 P 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 3 , 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.
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Reversible, Metal-Free Hydrogen Activation
Gregory C. Welch, Ronan R. San Juan, Jason D. Masuda et al. · Science · 2006 · 2.1K citations