N-Heterocyclic Carbene-Stabilized Germanium and Tin Analogues of Heavier Nitriles: Synthesis, Reactivity, and Catalytic Application

Abstract

The synthesis of stable heavier analogues of nitriles as monomeric tetrylene-phosphinidenes ^MesTerEP(IDipp) (E = Ge, Sn; ^MesTer = 2,6-Mes₂C₆H₃, IDipp = C([N-(2,6-<i>i</i>Pr₂C₆H₄)CH]₂) was achieved by taking advantage of NHC (N-heterocyclic carbene, here IDipp) coordination to the low-valent phosphorus center. Multiple bonding character of the E-P bonds was examined experimentally and computationally. Both germanium and tin compounds undergo [2+2] cycloaddition with diphenylketene, whereas reaction of the tin derivative with <i>tris</i>(pentafluorophenyl)borane provided unique "push-pull" phosphastannene (^MesTer)(Ar)Sn = P(IDipp) (Ar = C₆F₄[B(F)(C₆F₅)₂]). Going further, we demonstrated the potential of tetrylene-phosphinidene complexes in catalytic hydroboration of carbonyl compounds.