A mononuclear Dy^III complex with a non-Schiff base compartmental ligand has been prepared and characterised by X-ray crystallography and ac magnetic susceptibility measurements. The complex exhibits SIM behaviour induced by dilution and/or magnetic field with two thermally activated relaxation processes.

Nitrogen-containing heteroaromatic cores are ubiquitous building blocks in organic chemistry. Herein, we present a family of metal-free intermolecular formal cycloaddition reactions that enable highly selective and orthogonal access to isoquinolines and pyrimidines at will. Applications of the products are complemented by a density functional theory mechanistic analysis that pinpoints the crucial factors responsible for the selectivity observed, including stoichiometry and the nature of the heteroalkyne.

Chiral stapled o -OPEs show excellent circular polarized luminescence responses ( g _lum of 1.1 × 10 ⁻² ) which can be modulated by carbophilic interactions.