Abstract
AbstractTetraarylmethanes and adamantanes are important rigid covalent connectors that play a four‐way scaffolding role in molecular and materials chemistry. We report the synthesis of a new tetravalent phosphaza‐adamantane cage, (PNSiMe3)4(NMe)6 (2), that shows high thermal, air, and redox stability due to its geometry. It nevertheless participates in covalent four‐fold functionalization reactions along its periphery. The combination of a robust core and reactive corona makes 2 a convenient inorganic scaffold upon which tetrahedral molecular and macromolecular chemistry can be constructed. This potential is demonstrated by the synthesis of a tetrakis(bis(phosphine)iminium) ion (in compound 3) and the first all P/N poly(phosphazene) network (5).
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