Multi-site reduction of hexachlorophosphazene to low-valent PN heterocycles and extension to the reduction of poly-chlorophosphazene.

Facile one and two site reduction of hexachlorophosphazene using cyclic (alkyl)(amino)carbene substituents are shown to yield P-CAACMe-cyclo-(PNP(Cl)2NP(Cl)2N) 1 and P,P'-bis-CAACMe-cyclo-(PNPNP(Cl)2N) 2 (CAACMe = 1-[2,6-bis(isopropyl)phenyl]-3,3,5,5-tetramethyl-2-pyrrolidinylidene), respectively. Compound 1 is characterized by its predominantly phosphorus-centered HOMO, which results in typical phosphine-type nucleophilic and reductive reactivity; however, the resultant compounds of such reactions feature properties distinct from their classical phosphine analogues due to the CAAC-centered LUMO, which acts as an acceptor for both intramolecular interactions and photophysical excitations. In contrast, compound 2 exhibits π-conjugation spanning the endocyclic PNP moiety and the two CAACMe substituents, despite its non-planar structure. Treatment of 2 with [Cp*RuCl]4 results in the electrophilic displacement of one of the CAACMe moieties by two Cp*RuCl fragments to yield the spirocyclic compound 3. Preliminary results show that the methodology used to reduce hexachlorophosphazene to 1 can be directly transposed to the regiospecific reduction of poly-chlorophosphazene, to yield poly-1, a fundamentally new class of inorganic polymer that possesses a phosphorus center with chemically active lone pairs in the main chain.