Alkenylborane-Derived Frustrated Lewis Pairs: Metal-Free Catalytic Hydrogenation Reactions of Electron-Deficient Alkenes

Abstract

A series of alkenylboranes were prepared by 1,1-carboboration routes and used as Lewis acid components for the generation of frustrated Lewis pairs (FLPs). The reactions of 1-alkynes with B(C6F5)3 gave the RCH═C(C6F5)B(C6F5)2 systems 4a(R = n-C3H7), 4b (R = n-C4H9), 4c (R = Ph), and 4d (R = t-C4H9), respectively. The alkenylborane/tBu3P FLPs derived from compounds 4a–d reacted rapidly with dihydrogen (2.5 bar) at ambient temperature. The bulky system 4d left the C═C double bond of the alkenylborane unsaturated and gave the dihydrogen cleavage product [tBu3PH][tBuCH═C(C6F5)BH(C6F5)2] (10d). In contrast, the less bulky systems 4a/tBu3P and 4b/tBu3P split dihydrogen under these conditions and had their C═C double bonds cleanly reduced to yield the corresponding 1-pentafluorophenylalkyl hydridoborate salts [tBu3PH][RCH2CH(C6F5)BH(C6F5)2] 9a (R = n-C3H7) and 9b (R = n-C4H9), respectively. The 4c/tBu3P FLP gave a mixture of both product types (9c/10c). 1,1-Carboboration of symmetrical internal alkynes gave the alkenylboranes R2C═C(C6F5)B(C6F5)24e (R = C2H5), 4f (R = n-C3H7), 4g (R = Ph), and 4h (R = p-MeC6H4), respectively. The 4e–h/tBu3P FLPs cleaved dihydrogen under mild conditions but retained their C═C double bonds to give the respective [tBu3PH][R2C═C(C6F5)BH(C6F5)2] products (10e–h). Selected examples of these alkenylboranes undergo FLP reactions acting as catalysts for the hydrogenation of imines. Perhaps most remarkably, some of these alkenylboranes retain the C═C double bonds under FLP/H2 reaction conditions and heterolytically split dihydrogen in the presence of the Lewis base DABCO and catalyze the hydrogenation of the electron-poor C═C double bonds of diaryl-substituted enones.