Development of silica-supported frustrated Lewis pairs: highly active transition metal-free catalysts for the Z-selective reduction of alkynesElectronic supplementary information (ESI) available: NMR spectra, IR spectra, reaction scheme, catalytic graphics depicting 3-hexyne conversion and product selectivity, and gas chromatograms. See DOI: 10.1039/c5cy01372k

Supported Lewis acid/base systems based on a triphenyl phosphine fragment and Piers' reagent (HB(C 6 F 5 ) 2 ) or BArF have been prepared and characterized. Both materials show unprecedented catalytic activity in the Z -selective hydrogenation of 3-hexyne to Z -3-hexene with a selectivity up to 87%. Other alkynes can also be hydrogenated Z -selectively, albeit with moderate yields. The activity of the supported phosphine/HB(C 6 F 5 ) 2 adduct is similar to the only homogeneous example reported thus far based on bridged B/N frustrated Lewis pairs under high hydrogen pressure. Importantly, this transition metal-free supported catalyst was recycled five times in the challenging selective hydrogenation of a non-polar unactivated alkyne. Supported Lewis acid/base systems based have been prepared and characterized.