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N-Heterocyclic carbene ligands bearing a naphthoquinone appendage: Synthesis and coordination chemistry
Many biochemical transformations for small molecule functionalisation depend on the temporal delivery of multiple protons and electrons. For this purpose, Nature elegantly combines transition metals with redox-active cofactors. In a biomimetic spirit, we report on the synthesis and coordination chemistry of an N-heterocyclic carbene ligand bearing a naphthoquinone moiety NHC 1. Both the silver and palladium complexes [Ag(mu-Cl)(NHC 1)]2 2 and [Pd(eta3-allyl)(NHC 1)Cl] 5 were characterized by X-ray crystallography. Cyclic voltammetry of the metal complexes suggest that redox events occur both on the naphthoquinone and on the metal for the iridium and ruthenium complexes.
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Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI