Synthesis and isolation of a cyclic bis-vinyl germylene a diazoolefin adduct of germylene dichloride.

Since the successful isolation of various stable diazoolefins, an array of complexes containing these promising ligands have been synthesized. We herein report the synthesis, characterization, and structures of neutral group 14 diazoolefin complexes and the subsequent transformation into a new cyclic bis-vinyl germylene.

Room-Temperature-Observable Interconversion Between Si(IV) and Si(II) via Reversible Intramolecular Insertion Into an Aromatic C-C Bond.

An easily isolable silacycloheptatriene (silepin) 1 b was synthesized from the reaction of a N-heterocyclic imino (IPrN) substituted tribromosilane IPrNSiBr with the sterically congested bis(trimethylsilyl)triisopropylsilyl silanide KSi(TMS) Si( Pr) (BTTPS). In solution, the Si(IV) silepin 1 b is in a thermodynamic equilibrium with the acyclic Si(II) silylene 1 a. The relative concentration of the Si(II) or Si(IV) isomers can be controlled by temperature variation and observed by variable temperature NMR and UV/Vis spectroscopy.