Differences in the Reactivity of Geminal Si−O−P and Al−O−P Frustrated Lewis Pairs

The new oxygen‐bridged geminal Si/P Frustrated Lewis Pair (FLP) tBu2P−O−Si(C2F5)3 (2) is able to reversibly bind carbon dioxide at ambient temperature. We compared its reactivity towards benzil, but‐3‐en‐2‐one, nitriles and phenylacetylene to that of the Al/P FLP tBu2P−O−AlBis2 (Bis=−CH(SiMe3)2) (1). When reacted with benzil, both, 1 and 2, form the 1,2‐addition product, but in the Si/P FLP 2, the second carbonyl function additionally binds to the silicon atom. With but‐3‐en‐2‐one 2 forms the 1,2‐addition product, while 1 binds in 1,4‐position. The reaction with acetonitrile yielded an unexpected etheneimine adduct for both systems, while only 1 reacted with tert‐butylnitrile. With benzonitrile and acrylonitrile, 2 showed reversible addition to the C≡N bond and 1 forms a stable adduct with benzonitrile. Solely 1 shows reactivity towards phenylacetylene affording a mixture of the CH deprotonation adduct tBu2P(H)−O−AlBis2(CCPh) and the FLP −C≡C 1,2‐addition adduct under ring formation. All compounds were characterized by multinuclear NMR spectroscopy, XRD and elemental analysis. Variations in reactivity are observed for the geminal Si−O−P and Al−O−P Frustrated Lewis Pairs tBu2P−O−Si(C2F5)3 and tBu2P−O−Al(CH(SiMe3)2)2 towards CO2, nitriles and alkynes regarding regioselectivity, structure and stability of the corresponding adducts.