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.