Phosphoramidate-Supported Cp∗Ir^III Aminoborane H<inf>2</inf>B=NR<inf>2</inf> Complexes: Synthesis, Structure, and Solution Dynamics

Reaction of aminoboranes H2B=NR2 (R=iPr or Cy) with the cationic Cp∗IrIII phosphoramidate complex [IrCp∗{κ2-N,O-Xyl(N)P(O)(OEt)2}][BArF4] generates the aminoborane complexes [IrCp∗(H){κ1-N-η2-HB-Xyl(N)P(OBHNR2)(OEt)2}][BArF4] (R=iPr or Cy) in which coordination of a P=O bond with boron weakens the B=N multiple bond. For these complexes, solution- and solid-state, as well as DFT computational techniques, have been employed to substantiate B-N bond rotation of the coordinated aminoborane.