Prior to the year 2000, non‐aqueous uranium chemistry mainly involved metallocene and
classical alkyl, amide, or alkoxide compounds as well as established carbene, imido, and …

In the last few years, considerable progress has been made in the synthesis and
characterization of complexes containing actinide–ligand multiple bonds, especially in …

The terminal uranium nitride linkage is a fundamental target in the study of f-orbital
participation in metal-ligand multiple bonding but has previously eluded characterization in …

Most homogeneous catalysis relies on the design of metal complexes to trap and convert
substrates or small molecules to value‐added products. Organometallic lanthanide …

The nature and extent of covalency in uranium bonding is still unclear compared with that of
transition metals, and there is great interest in studying uranium–ligand multiple bonds …

Metallonitrenes (M–N) are complexes with a subvalent atomic nitrogen ligand that have
been proposed as key reactive intermediates in nitrogen atom transfer reactions. However …

Uranium nitrides play important roles in dinitrogen activation and functionalization and in
chemistry for nuclear fuels, but the synthesis and isolation of the highly reactive uranium (VI) …

C–H functionalization is a fundamentally important organic transformation to access C–C
and C–heteroatom bonds in a common and/or complex molecular set-up during the …

Actinide coordination chemistry is currently experiencing a renaissance, with the emergence
of exciting and less studied oxidation states, and previously unpredicted magnetic properties …

Coupling reactions of nitrogen atoms represent elementary steps to many important
heterogeneously catalysed reactions, such as the Haber–Bosch process or the selective …