Quinoline-Tethered N-Heterocyclic Carbene Complexes of Rhodium and Iridium: Synthesis, Catalysis, and Electrochemical Properties

A series of rhodium and iridium complexes of quinoline-tethered hemilabile N-heterocyclic carbenes (NHC ∧ N) have been synthesized via either deprotonation of imidazolium salts or silver transmetalation. Deprotonation of imidazolium ions by t BuOK in the presence of [Rh(COD)Cl] 2 (COD = 1,5-cyclooctadiene) afforded both chelating [Rh(COD)(NHC ∧ N)] + and monodentate [Rh(COD)(NHC) 2 ] + complexes, while only the chelating carbene complexes were obtained for the iridium analogues. Silver transmetalation of this type of carbene to [M(COD)Cl] 2 (M = Rh, Ir) consistently afforded M(NHC)(COD)Cl, maintaining the metal chloride and pendant quinoline entity. Carbene transmetalation to (Cp ∗ IrCl 2 ) 2 gave an equilibrium mixture of neutral Cp*Ir(NHC)Cl 2 and ionic [Cp*Ir(NHC ∧ N)Cl]Cl. All these rhodium and iridium cyclooctadiene complexes can undergo one-electron oxidation in cyclic voltammetry. The variable-scan-rate cyclic voltammetry experiments indicate that these compounds undergo slow heterogeneous electron transfer and that the oxidized forms are relatively short-lived. A neutral Rh(COD)(NHC)Cl complex proved to be active in catalyzing the [3 + 2] cycloaddition reactions of diphenylcyclopropenone and internal alkynes. Crystal structures of metal complexes in each category have been reported.