Light-driven C-H activation mediated by 2D transition metal dichalcogenides
Project Summary: The activation and functionalization of C-H bonds enables new synthetic routes for functional molecules. Since C-H bonds are thermodynamically strong, metal catalysts such as Pd, Co, Au, etc. in combination with a zeolite or metalorganic framework are typically employed. Here we report light-driven C-H activation in complex organic molecules mediated by 2D transition metal dichalcogenides (TMDs). The process involves efficient hydrogen adsorption and a lowered energy barrier of C-C coupling mediated by TMDs.
