Half-Sandwich Ru(II)Complexes Featuring Metal-CenteredChirality: Configurational Stabilization by Ligand Design, Preparationvia Kinetic Resolution, and Application in Asymmetric Catalysis

While it is well established that half-sandwich Ru(II) complexes possess metal-centered chirality, effective strategies to leverage their metal-centered chirality toward asymmetric synthesis have been challenging due to the configurational lability of the metal stereocenters. The metal-centered chirality is typically mediated by enantiopure ligands, which occupy a relatively narrow chemical space compared to their achiral counterparts. We demonstrate that achiral ligands can be used to access chiral-at-ruthenium half-sandwich complexes with exceptionally high configurational stability. Key to success is the introduction of a rigid bidentate ligand with a minimized dihedral angle between the pyridyl and phenolic moieties, which proved effective for preventing racemization. Computational studies revealed the energetic factors contributing to the exceptional configurational stability enabled by the rigid and planar structure of the successful ligand design. These optically active chiral-at-ruthenium complexes incorporating aldehyde moieties were obtained by NHC-catalyzed kinetic resolution with excellent selectivities (<i>s</i>-factor up to >200, ee up to 99%). We further demonstrate that they are highly effective chiral aldehyde catalysts for the asymmetric 1,6-conjugate addition of glycine ester and <i>para</i>-quinone methide.