The novel amphipilic conjugate of a calix[4]arene with four Gd–1,4,7,10‐ tetra(carboxymethyl)‐1,4,7,10‐tetraazacyclododecane (DOTA) chelates has potential as a magnetic resonance imaging contrast agent, both in its monomeric and in its micellar form. The system, illustrated here with its nuclear magnetic relaxation profile, shows good relaxivities, thanks to its high rigidity.
Just five steps! The synthesis of a phosphonate‐linked aminoglycoside‐coenzyme A derivative (see scheme) that includes a Michael addition in water has been realized in just five steps.
Clicking in zeolites : Copper(I)‐exchanged zeolites proved to be practical and efficient catalysts for the cycloaddition of azomethine imines with alkynes, providing a convenient access to N,N‐bicyclic pyrazolidinone derivatives (see scheme). With high regioselectivity, 100 % atom economy, and convenient product isolation, this heterogeneously catalyzed version of the Dorn cycloaddition corresponds to click‐chemistry criteria.
Trifunctional green catalysis : In‐depth characterization shows that oxidant‐free selective oxidation of alcohols by silver nanoparticles on γ‐Al2O3, as a new heterogeneous catalyst, proceeds through cooperation of silver, acid, and base sites (see figure).
How deep is your orbital? Density functional theory studies on the axial ligand effect of aliphatic versus aromatic hydroxylation of ethylbenzene by iron–oxo complexes with a variable axial ligand show that strong (anionic) ligands pull the metal inside the plane of the haeme and destabilise cationic intermediates through orbital interactions (see picture).
