Reversible C−H Activation, Facile C−B/B−H Metathesis and Apparent Hydroboration Catalysis by a Dimethylxanthene‐Based Frustrated Lewis Pair

Abstract

A dimethylxanthene-based phosphine/borane frustrated Lewis pair (FLP) is shown to effect reversible C-H activation, cleaving phenylacetylene, PhCCH, to give an equilibrium mixture of the free FLP and phosphonium acetylide in CD₂ Cl₂ solution at room temperature. This system also reacts with B-H bonds although in a different fashion: reactions with HBpin and HBcat proceed via C-B/B-H metathesis, leading to replacement of the -B(C₆ F₅ )₂ Lewis acid component by -Bpin/-Bcat, and transfer of HB(C₆ F₅ )₂ to the phosphine Lewis base. This transformation underpins the ability of the FLP to catalyze the hydroboration of alkynes by HBpin: the active species is derived from the HB(C₆ F₅ )₂ fragment generated in this exchange process.