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Room temperature reaction of the uranium(iv)-carbene [U{C(SiMe3)(PPh2)}(BIPMTMS)(μ-Cl)Li(TMEDA)(μ-TMEDA)0.5]2 (1, BIPMTMS = C(PPh2NSiMe3)2) with white phosphorus (P4) produces the organo-P5 compound [P5{C(SiMe3)(PPh2)}2][Li(TMEDA)2] (2) and the uranium(iv)-methanediide [U{BIPMTMS}{Cl}{μ-Cl}2{Li(TMEDA)}] (3). This is an unprecedented example of cooperative metal-carbene P4 activation/insertion into a metal-carbon double bond and also an actinide complex reacting with P4 to directly form an organophosphorus species. Conducting the reaction at low temperature permits the isolation of the diuranium(iv) complex [{U(BIPMTMS)([μ-η2:η2-P2]C[SiMe3][PPh2])}2] (4), which then converts to 2 and 3. Thus, surprisingly, in contrast to all other actinide P4 reactivity, although this reaction produces catenation overall it proceeds via P4 cleavage to functionalised P2 units. Hence, this work establishes a proof of concept synthetic cycle for direct fragmentation, catenation, and functionalisation of P4.

Fragmentation, catenation, and direct functionalisation of white phosphorus by a uranium(iv)–silyl–phosphino–carbene complex