Iridium α-Carboxyimine Complexes Hyperpolarized with para-Hydrogen Exist in Nuclear Singlet States before Conversion into Iridium Carbonates.

The formation and hyperpolarization of an [Ir(H) (amine)(IMes)(η -imine)]Cl complex that can be created in a hyperpolarized nuclear singlet state is reported. These complexes are formed when an equilibrium mixture of pyruvate, amine (benzylamine or phenylethylamine), and the corresponding imine condensation product, react with preformed [Ir(H) (amine) (IMes)]Cl. These iridium α-carboxyimine complexes exist as two regioisomers differentiated by the position of amine. When examined with para-hydrogen the hydride resonances of the isomer with amine trans to hydride become strongly hyperpolarized. The initial hydride singlet states readily transfer to the corresponding C state in the labelled imine and exhibit magnetic state lifetimes of up to 11 seconds. Their C signals have been detected with up to 420 fold signal gains at 9.4 T. On a longer timescale, and in the absence of H , further reaction leads to the formation of neutral carbonate containing [Ir(amine)(η -CO )(IMes)(η -imine)]. Complexes are characterized by, IR, MS, NMR and X-ray diffraction.