The review is devoted to compounds and materials demonstrating extremely high magnetic hardness. The recent advances in the synthesis of modern materials for permanent magnets are considered, and a range of exotic compounds interesting for fundamental research is described. The key details of chemical composition, crystal structure and magnetic microstructure responsible for the appearance of high magnetic anisotropy and giant coercivity are analyzed. The challenges of developing the title materials are noted and strategies for their solution are discussed.The bibliography includes 389 references.

Magnetically hard ferrites attract considerable interest due to their ability to maintain a high coercivity of nanosized particles and therefore show promising applications as nanomagnets ranging from magnetic recording to biomedicine. Herein, we report an approach to prepare nonsintered single-domain nanoparticles of chromium-substituted hexaferrite via crystallization of glass in the system SrO–Fe₂O₃–Cr₂O₃–B₂O₃. We have observed a formation of plate-like hexaferrite nanoparticles with diameters changing from 20 to 190 nm depending on the annealing temperature. We demonstrated that chromium substitution led to a significant improvement of the coercivity, which varied from 334 to 732 kA m⁻¹ for the smallest and the largest particles, respectively. The results provide a new strategy for producing high-coercivity ferrite nanomagnets.

Synthesis optimisation and a reproducibility study of the titanium-based MOF NTU-9 with a detailed ( in situ ) characterisation lead to the discovery of its flexibility upon external stimuli ( e.g. , vacuum) and the new distorted form NTU-9-d.

Solid-state studies evaluating intermolecular geometries in methylated nucleobases are not extensively explored. In the course of the present study, we have solved the crystal structures of 1-, 3- and 7-methylated adenines and guanines, including the monohydrate and sesquihydrate forms of 3-methyladenine and 3-methylguanine, respectively, by means of single-crystal X-ray diffraction and synchrotron/laboratory X-ray powder diffraction (XRPD). In situ high temperature XRPD experiments, coupled with differential thermal analysis/thermogravimetry (DTA/TG) measurements, allowed for monitoring crystallographic changes after water removal of N3-methylated compounds, and the discovery of a high temperature polymorph in the case of 3-methyladenine. Our findings indicate that H-bonding schemes describe ribbon planar motifs of molecules in the majority of cases, or linear double-bonded strands of molecules in a few cases. π-π stacking interactions were compared with existing findings of theoretical calculations and existing crystallographic data, showing how N-methylated purine bases follow the trend predicted by Hunter and Sanders, 1990. The present study provides the first systematic experimental insights into the solid state of the presented compounds.