Versatile Tautomerization of EH-Substituted Silylenes (E = N, P, As) in the Coordination Sphere of Nickel.

The synthesis and tautomerization of a "half-parent" aminosilylene and its heavy P- and As-analogues (LSi-EH; E = N, P, As; L = N(SiMe)(2,6- PrCH)) in the coordination sphere of nickel(0) to give the corresponding side-on η-RSi(H)═EH and RHSi-E ("silylpnictinidene") nickel complexes are reported. These complexes can be accessed through salt metathesis reactions of the lithium dihydropnictides LiEH with the acyclic chlorosilylene nickel(0) complex 1, [L(Cl)Si → Ni(NHC); NHC = :C[( Pr)NC(Me)]). In addition, we report the facile E-H bond activation reactions of EH with 1, which furnished a silyl nickel(II) complex through NH activation, but phosphido and arsenido complexes in the activation of PH and AsH, respectively. Notably, reaction of 1 with LiNH leads to the acyclic bis(amido)silylene complex [L(HN)Si → Ni(NHC)] 5, which does not undergo N-H proton migration to silicon(II) under ambient conditions. The transformation of the P- and As-analogues of 1 furnishes directly the respective side-on Si═E Ni complexes (nickelacycles), [η-{L(H)Si═E(H)}Ni(NHC)] (E = P, 6; E = As, 9). These nickelacycles show a vastly different stability in solutions. While 6 is stable for several days at ambient temperature, 9 undergoes further rearrangement processes within minutes of its formation. Given the high acidity of the As-H proton in 9, however, this moiety can be trapped as a highly charge separated metalated-η-silaarsene nickel complex 12 that is best described as an [AsSiNi] nickelacycle with Si-As multiple bond character. Taken as a whole, these results give, for the first time, insights into the relative stability of the tautomeric forms of side-on silaldimine transition metal complexes. The electronic nature and the rearrangement processes of these compounds were also investigated by quantum chemical calculations.