Abstract
AbstractHexacoordinate (arenediolato)silicon(IV) complexes that contain two additional 2,2′‐bipyridine or 1,10‐phenanthroline ligands are surprisingly stable against aqueous hydrolysis and therefore constitute attractive and novel templates for the design of bioactive compounds. In this article, we report the synthesis of (arenediolato)bis(polypyridyl)silicon(IV) complexes, including a case of diastereoselective synthesis of a nonracemic hexacoordinate (binaphtholato)silicon(IV) complex, and methods for their post‐coordinative functionalization with halides, nitro, and carbonyl groups. Several X‐ray crystal structures are provided and demonstrate the octahedral coordination of silicon in these complexes.
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