Synthesis, structure and isomerization of A2SiSiB2-type tetrakis(trialkylsilyl)disilenes

Two novel A2SiSiB2-type tetrakis(trialkylsilyl)disilenes: 3(A=t-BuMe2Si, B=i-Pr2MeSi) and 4 (A=t-BuMe2Si, B=i-Pr3Si) were synthesized in good yields. X-ray structural analysis revealed that both 3 and 4 have a twisted SiSi double bond with a planar arrangement around each of the unsaturated silicon atoms. The twist angle around the SiSi double bond is remarkably dependent on the substituents and amounts to 27.95(3)° for highly congested disilene 4. Disilene 3 underwent gradually a formal dyotropic rearrangement of trialkylsilyl substituents to give an equilibrium mixture of 3 and (E)- and (Z)-isomers of the corresponding ABSiSiAB-type disilenes (2E and 2Z). The activation energy for the isomerization of 3 to 2Z and/or 2E was found to be much smaller than that for the corresponding isomerization of a tetraaryldisilene system.