This feature article provides an overview of the application of organic azides for the intermolecular amination of sp(3) and sp(2) C-H bonds. The catalytic activity of several metal complexes was reviewed underlining both synthetic and mechanistic aspects of the C-H amination. The majority of the aminated compounds reported in literature have been collected in this paper to provide a compendium of published procedures. In addition, the discussion of involved mechanisms has been included to assist the reader to envisage the future potential of organic azides in the synthesis of aza-derivatives.

The use of secondary interactions between substrates and catalysts is ap romising strategy to discover selective transition metal catalysts for atom-economy CÀHb ond functionalization. The most powerful catalysts are found via trial-and-error screening due to the low association constants between the substrate and the catalyst in whichs mall stereoelectronic modifications within them can lead to very different reactivities.T ocircumvent these limitations and to increase the level of reactivity prediction in these important reactions,w e report herein as upramolecular catalyst harnessing Zn•••N interactions that binds to pyridine-like substrates as tight as it can be found in some enzymes.T he distance and spatial geometry between the active site and the substrate binding site is ideal to target unprecedented meta-selective iridium-catalyzed CÀHb ond borylations with enzymatic Michaelis-Menten kinetics,b esides unique substrate selectivity and dormant reactivity patterns.

Enantiomeric excess (ee) determination is crucial in many aspects of science, from synthesis to materials. Within this subject, coupling molecular sensors with chiroptical techniques is a straightforward approach to the stereochemical analysis of chiral molecules, especially in terms of process immediacy and labor. Stereodynamic probes typically consist of racemic mixtures of rapidly interconverting enantiomeric conformers able to recognize a chiral analyte and greatly amplify its chiroptical readout. A great number of sensors have been developed, but their activity is generally restricted to one or a few classes of chemicals, and the analysis outcome relies on precise knowledge of the probe and analyte concentrations. This aspect in particular limits the potential practical applications. Here we report an oxo-vanadium(V) aminotriphenolate complex that was found to act as a concentration-independent stereodynamic sensor for a wide range of compounds. The bare complex is CD-silent, but coordination of an enantioenriched substrate immediately gives rise to intense Cotton effects in the visible region. Furthermore, a geometry change during the substrate-complex interaction leads to a marked optical response, as witnessed by a strong red-shift of the probe absorption bands, thus allowing the generation of dichroic signals in an "interference-free" area of the spectrum. This peculiarity allows for a linear correlation at high wavelengths between the ee of the analyte and anisotropy g-factor. This parameter derives from the differential circularly polarized light absorption of the sample but is independent of concentration. The newly developed sensor based on a simple coordination process has an unprecedented general character in terms of substrate scope and employment.

A mechanism for the aziridination of olefins by aryl azides (ArN3), promoted by ruthenium(ii) porphyrin complexes, is proposed on the basis of kinetic and theoretical studies. All the recorded data support the involvement of a mono-imido ruthenium complex as the active intermediate in the transfer of the nitrene moiety "ArN" to the olefin. The selectivity of the aziridination vs. the uncatalysed triazoline formation can be enhanced by fine-tuning the electronic features of the porphyrin ligand and the olefin/azide catalytic ratio. The DFT study highlights the importance of an accessible triplet ground state of the intermediate ruthenium mono-imido complex to allow the evolution of the aziridination process.