The iron­(II) complexes of two structural isomers of 2-(1H-imidazol-2-yl)­diazine reveal how ligand design can be a successful strategy to control the electronic and magnetic properties of complexes by fine-tuning their ligand field. The two isomers only differ in the position of a single diazinic nitrogen atom, having either a pyrazine (Z) or a pyrimidine (M) moiety. However, [Fe­(M)3]­(ClO4)2 is a spin-crossover complex with a spin transition at 241 K, whereas [Fe­(Z)3]­(ClO4)2 has a stable magnetic behavior between 2 and 300 K. This is corroborated by temperature-dependent Mössbauer spectra showing the presence of a quintet and a singlet state in equilibrium. The temperature-dependent single-crystal X-ray diffraction results relate the spin-crossover observed in [Fe­(M)3]­(ClO4)2 to changes in the bond distances and angles of the coordination sphere of iron­(II), hinting at a stronger σ donation of ligand Z in comparison to ligand M. The UV/vis spectra of both complexes are solved by means of the multiconfigurational wave-function-based method CASPT2 and confirm their different spin multiplicities at room temperature, as observed in the Mössbauer spectra. Calculations show larger stabilization of the singlet state in [Fe­(Z)3]2+ than in [Fe­(M)3]2+, stemming from the slightly stronger ligand field of the former (506 cm–1 in the singlet). This relatively weak effect is indeed capable of changing the spin multiplicity of the complexes and causes the appearance of the spin transition in the M complex.

Carbon dots (CDs) show extensive potential in various fields such as sensing, bioimaging, catalysis, medicine, optoelectronics, and drug delivery due to their unique properties, that is, low cytotoxicity, cytocompatibility, water-solubility, multicolor wavelength tuned emission, photo-stability, easy modification, strong chemical inertness, etc. This review article especially focuses on the recent advancement (2015–2022) in the green synthesis of CDs, their application in metal ions sensing and microbial bioimaging, detection, and viability studies as well as their applications in pathogenic control and plant growth promotion.

The first example of a homoleptic RuII complex with heteroaryl-imidazoles is reported in the meridional stereochemistry, exclusively. The supra­molecular hydrogen-bonded network reveals mutual N—H⋯N bonds between adjacent complexes.

The removal of water pollutants by photocatalysis is a promising technique, mainly due to its environmentally friendly and sustainable nature. In this study, the degradation of a recalcitrant organic pollutant, malachite green (MG), was investigated in water by a microstructured silver oxide photocatalyst. The silver oxide (Ag2O) microparticles (MPs) were synthesized by a low-cost, green method, mediated by green tea leaves extract. The surface, morphological and optical properties of the synthesized Ag2O MPs were determined by scanning electron microscopy (SEM), energy dispersive X-ray (EDX) analysis, X-ray diffraction (XRD) analysis, Fourier transform infrared (FTIR) spectroscopy, and ultraviolet-visible (UV-visible) spectrophotometry. The synthesized Ag2O MPs showed good photoactivity, represented by 83% degradation of malachite green (MG) ([C]0 = 0.4 mM, Ag2O loading = 0.1 g L−1) at neutral pH, in 3 h. Persulfate ions (PS) showed a strong synergistic effect on the efficiency of solar/Ag2O photocatalysis, represented by complete MG removal in 15 min, in the presence of 1.6 mM PS. The results revealed that solar/Ag2O, particularly solar/Ag2O/PS photocatalysis is a promising method for the elimination of toxic organic pollutants, such as malachite green, from the water environment.

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