Consecutive N2 loss from a uranium diphosphazide complex.

Abstract

A new 'diphosphazidosalen' ligand was synthesized and successfully transferred to uranium using salt metathesis strategies. The resultant 8-coordinate uranium(iv) diphosphazide complex [κ6-1,2-{(N3)PPh2(2-O-C6H4)}2C6H4]UCl2 (1) is unstable to consecutive N2 loss, affording the asymmetric species [κ5-1-{(N3)PPh2(2-O-C6H4)}-2-{N=PPh2(2-O-C6H4)}C6H4)]UCl2 (2), defined by a phosphazide-phosphinimine mixed-ligand framework, and ultimately, the uranium(iv) phosphasalen complex [κ4-1,2-{N=PPh2(2-O-C6H4)}2C6H4]UCl2(THF) (3).