A collective overview of iron(ii)-Schiff base complexes, showing abrupt and hysteretic SCO suitable for device applications, and the structure–property relationships governing the SCO of the complexes in the solid-state is presented.

The breakthrough in Ln(III)-based SMMs with Schiff base ligands have been occurred for the last decade on account of their magnetic behavior, anisotropy and relaxation pathways. Herein, we review the synthetic strategy, from a structural point of view and magnetic properties of mono, di, tri and polynuclear Ln(III)-based single-molecule magnets mainly with Schiff bases of Salicylaldehyde origin. Special attention has been given to some important breakthroughs that are changing the perspective of this field with a special emphasis on slow magnetic relaxation. An overview of 50 Ln(III)-Schiff base complexes with SMM behavior, covering the period 2008–2020, which have been critical in understanding the magnetic interactions between the Ln(III)-centers, are presented and discussed in detail.

Magnetically recyclable C-doped TiO2/Fe3O4 (C-TiO2/Fe3O4) nanocomposite was successfully synthesized via a sol–gel method. The synthesized samples were characterized using SEM, energy-dispersive X-ray spectroscopy (EDS), FTIR, and UV-VIS diffuse reflectance spectroscopy (DRS) techniques. The results clearly showed that a C-TiO2/Fe3O4 nanocomposite was produced. The photocatalytic activities of the prepared pristine (TiO2), C-doped TiO2 (C-TiO2) and C-TiO2/Fe3O4 were evaluated by the photodegradation of methyl orange (MO) under natural sunlight. The effect of catalyst loading and MO concentration were studied and optimized. The C-TiO2/Fe3O4 nanocomposite exhibited an excellent photocatalytic activity (99.68%) that was higher than the TiO2 (55.41%) and C-TiO2 (70%) photocatalysts within 150 min. The magnetic nanocomposite could be easily recovered from the treated solution by applying external magnetic field. The C-TiO2/Fe3O4 composite showed excellent photocatalytic performance for four consecutive photocatalytic reactions. Thus, this work could provide a simple method for the mass production of highly photoactive and stable C-TiO2/Fe3O4 photocatalyst for environmental remediation.

A tetranuclear dysprosium Schiff base complex was isolated by reacting dysprosium chloride with 2-hydroxy-3-methoxybenzaldehyde and 2-(aminomethyl)pyridine in-situ under basic conditions. The isolated Dy(III) complex was characterized by elemental analyses, single crystal X-ray diffraction and molecular spectroscopy. The complex crystallizes in the triclinic space group P-1 with unit cell parameters of a = 10.2003 (4), b = 13.8602 (5), c = 14.9542 (6), α = 94.523 (3), β = 109.362 (4), and γ = 99.861 (3). The magnetic properties of 1 have been investigated by DC and AC susceptibility measurements. The DC measurements reveal weak exchange coupling of antiferromagnetic nature. In the AC measurement, the complex shows a slow relaxation of magnetization in the absence of an external magnetic field.