The p K _a ¹ values and NBO charges of 32 carboxylate ligands and 31 N -heterocyclic ligands were calculated at 298.15 K with the B3LYP/6-31+G(d,p) level of calculations, which are useful to understand the water and thermal stability of Metal–Organic Frameworks (MOFs).

The first triradical bridged binuclear penta-spin single-molecule magnet, [Dy₂(hfac)₆(BTR)], based on a nitronyl nitroxide triradical was synthesized and characterized. Theoretical calculations revealed Dy-radical antiferromagnetic coupling and radical–radical ferromagnetic coupling. The SMM behavior is found to originate from the exchange states, rather than the isolated Dy³⁺ center.

The well-controlled structural motifs of zirconium metal–organic frameworks (Zr-MOFs) and their similarity to enzyme cofactors make them ideally suited for biomimetic catalysis. However, the activation methodologies for these motifs, the structural information about active conformations and the reaction mechanism during these biomimetic reactions, are largely unknown. Herein, we have explored the precise pH-controlled activation processes, active sites, and reaction mechanisms for a series of Zr-MOFs as alkaline phosphatase mimics. Activation of the Zr-MOFs with a broad range and precise changes of pH led to the discovery of the MOF-catalyzed volcano plot with activity versus pH changes. This unique response revealed the existence of the precisely pH-controlled active form of the material, which was confirmed with computational analysis using density functional theory and diffuse reflectance infrared Fourier transform spectroscopy. These results will open a window for state-of-the-art design of efficient MOF enzyme mimics in aqueous solution.

The reduction of molecular dinitrogen (N₂) to ammonia (NH₃) under mild conditions is attractive due to the wide application of ammonia.