We report two BNB-type frustrated Lewis pairs which feature an acceptor-donor-acceptor functionalized cavity, and which differ in the nature of the B-bound fluoroaryl group (C F vs. C H (CF ) -3,5, Ar ). These receptor systems are capable of capturing gaseous CO, and in the case of the -BAr system this can be shown to occur in reversible fashion at/above room temperature.
View Article and Find Full Text PDFA 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 CD Cl 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(C F ) Lewis acid component by -Bpin/-Bcat, and transfer of HB(C F ) 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(C F ) fragment generated in this exchange process.
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