Artificial Metalloenzymes with Multiple Catalytic Sites for Tandem or Synergistic Transformations

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N-Heterocyclic carbenes (NHCs) are preferred ligands in numerous transformations involving various transition metals. Despite their broad utility, the availability of chiral NHCs for asymmetric catalysis is limited. However, a chiral version of the widely ...

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Cu-based bimetallic catalysts have attracted great attention for the reverse water gas shift (RWGS) reaction due to their high activity and selectivity. This work reports the application of Cu-In bimetallic catalysts for the RWGS reaction and demonstrates ...

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The enantiopure Schiff bases (R or S)-N-1-( phenyl)ethyl-2,4-X-1,X2(-)salicylaldimine (X-1, X-2 = Cl, Br, I) coordinate to copper(II) and provide pseudotetrahedral bis[(S or R)-N-1-(phenyl)ethyl-(2,4-X-1,X-2-salicylaldiminato.2N,O)]-./.-Cu(II) (kappa N-2,O ...

Artificial Metalloenzymes with Multiple Catalytic Sites for Tandem or Synergistic Transformations

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Efficient Direct Cytosolic Protein Delivery via Protein-Linker Co-engineering

Chiral N-Heterocyclic Carbene Ligands: Enhancing Nickel-Catalyzed Asymmetric Syntheses

Anisotropic In-Plane strain engineering Ni(OH)2 to activate alkaline hydrogen evolution reaction

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Support-Dependent Cu-In Bimetallic Catalysts for Tailoring the Activity of Reverse Water Gas Shift Reaction

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Solid-state to solution helicity inversion of pseudotetrahedral chiral copper(II) complexes with 2,4-dihalo-salicylaldiminate ligands