Antioxidant activity of Schiff base ligands using the DPPH scavenging assay: an updated review.

Schiff base ligands, formed from primary amines and carbonyl compounds, are potential antioxidants because they scavenge 2,2-diphenyl-1-picrylhydrazyl (DPPH) radicals hydrogen atom transfer (HAT) and single electron transfer (SET) routes. This review aims to help design, synthesize, and discuss the antioxidant activity of Schiff base ligands based on their structure. This study critically discussed the solvent effect and the structural changes of Schiff base ligands responsible for DPPH scavenging activity, such as proton donating, electron-donating, and electron-withdrawing substituents, conjugation and ring structure.

Water-soluble Schiff base ligands and metal complexes: an overview considering green solvent.

The water-soluble metal complexes with Schiff base (SB) ligands are of great interest to green chemistry researchers due to their stability, cost-effectiveness, eco-friendly, electron-donating ability, and various applications. They have high potential to express their biological activity including anti-inflammatory, anticancer, antibacterial, antifungal, antioxidant, and DNA binding and cleavage. In the recent era, transition metal complexes have played a significant role in different processes such as hydrogenation, carbonylation, oxidation, reduction, epoxidation, hydrolysis, decomposition, and polymerization reactions in industry.

Homogeneous photochemical water oxidation with metal salophen complexes in neutral media.

The development of water oxidation catalysts based on Earth-abundant metals that can function at neutral pH remains a basic chemical challenge. Here, we report that salophen complexes with Ni(ii), Cu(ii), and Mn(ii) can catalyse photochemical water oxidation to molecular oxygen in the presence of [Ru(bpy)] as a photosensitizer and NaSO as an oxidant in phosphate buffer of pH 7.0.

Cationic nickel metal-organic frameworks for adsorption of negatively charged dye molecules.

Industrial dye effluents with low biodegradability are highly toxic and carcinogenic on both human and aquatic lives, thus they are detrimental to the biodiversity of environment. Herein, this data set presents the potential of cationic Nickel based MOFs in the adsorption of charged and neutral dye molecules. Data set include a concise description of experimental conditions for the synthesis of imidazolium ligands, 1,3-bis(4-carboxyphenyl)imidazolium chloride (HLCl) and 1,3-bis(3,5-dicarboxyphenyl)imidazolium chloride (HLCl), and MOFs.

Selective and adsorptive removal of anionic dyes and CO with azolium-based metal-organic frameworks.

The positively charged azolium moieties make imidazolium linker an ideal linker for the construction of cationic metal-organic frameworks because the ligand induces cationic environments in the frameworks. Therefore, we employed two imidazolium ligands, 1,3-bis(4-carboxyphenyl)imidazolium chloride (HLCl¯) and 1,3-bis(3,5-dicarboxyphenyl)imidazolium chloride (HLCl¯), to synthesize two nickel azolium-based MOFs, 1 and 2. The as-synthesis MOFs were characterized by PXRD, TGA, FE-SEM, HR-TEM, FTIR and BET measurements.