Abstract
The reaction of ((2,2-dimethyl-1-(trimethylsiloxy)propylidene)-trimethylsilylphosphine], 1, with pentaborane(9) under mild conditions produced the bridged phosphinopentaborane cluster ((tBu) (Me3SiO)HCP(SiMe3))B5H8, 2, in high yield. This phosphaborane reacts readily with water to quantitatively produce the corresponding P—H substituted cage compound ((tBu)(Me3SiO)HCP(H))B5H8, 3, via an electrophilic exopolyhedral substitution reaction at the phosphorus atom. All new compounds have been characterized by a variety of spectroscopic methods including 1H, 13C, 11B, 31P NMR, FT-IR and mass spectroscopic analysis.