The Addition of Nitriles to a Molecular Digermene: Reversible Addition and Comparison to Surface Reactivity

Abstract

The addition of acetonitrile, propionitrile, and acrylonitrile to tetramesityldigermene was investigated and compared to the addition of acetonitrile and acrylonitrile to germanium dimers on the Ge(100)‐2×1 surface. In each case, a 1,2,3‐azadigermetine was formed as the major product. As on the surface, the addition of nitriles to digermenes was found to be reversible, providing the first example of a reversible cycloaddition of a ditetrelene. No evidence for a six‐membered cyclic ketenimine was observed as noted in the surface chemistry, suggesting that the surface ketenimine might only form between two adjacent dimers rather than on a single dimer. The comparative chemistry provides important insights that are not possible by the independent study of each system.

Reversibility in Reactions of Linker-Bridged Distannenes with Terminal Alkynes at Ambient Temperature

“…Only recently, to our knowledge, has the first example of a cycloaddition reaction of a digermene with nitriles which shows reversibility at 100 °C been reported …”