C–H activation has surfaced as an increasingly powerful tool for molecular sciences, with
notable applications to material sciences, crop protection, drug discovery, and …

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

Though often perceived as the simple metaphorical hybrid of synthetic inorganic and
organic chemistry, synthetic organometallic chemistry continues to vigorously differentiate …

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 …

The chemistry of actinide (An) and rare-earth metal (Ln and group 3) complexes featuring
multiple bonding interactions with main-group fragments has witnessed an enormous …

In the present review advances in the metal-catalyzed 1, 3-dipolar cycloaddition reactions of
nitrile oxides, mainly in the last decade, will be presented and discussed. An overview on …

Cyclometalative C–H bond activation is a process that is commonly encountered in the field
of organometallic chemistry. In rare earth and actinide complexes, ligand cyclometalation is …

Terminal rare-earth-metal imide complexes TptBu, MeLn (NC6H3iPr2-2, 6)(dmap) of the mid-
late rare-earth elements dysprosium and holmium were synthesized via double methane …

Group 3-and 4f-element organometallic chemistry and reactivity are decisively driven by the
rare-earth-metal/lanthanide (Ln) ion size and associated electronegativity/ionicity/Lewis …

The first rare earth metal terminal imido complex has been isolated and structurally
characterized. The complex has an extremely short M–N bond length and a nearly linear M …