Removal, mechanistic and kinetic studies of Cr(VI), Cd(II), and Pb(II) cations using FeO functionalized Schiff base chelating ligands.

The Schiff base chelating ligands; (E)-2-(3,3-dimethoxy-2-oxa-7,10-diaza-3-silaundec-10-en-11-yl)phenol (L1), (E)-N-(2-((pyridine-2ylmethylene)amino)ethyl)-3-(trimethoxysilyl)propan-1-amine (L2) and (E)-N-(2-((thiophen-2-ylmethylene)amino)ethyl)-3-(trimethoxysilyl)propan-1-amine (L3) were immobilized on FeO magnetic nanoparticles (MNPs) and utilized in the extraction of Cr(VI), Cd(II) and Pb(II) metal cations from aqueous solutions. The compounds synthesized, denoted as L1@ FeO, L2@FeO, and L3@FeO, were characterized using FT-IR spectroscopy, TEM-SEM, VSM, and BET/BHJ techniques for analysis of functional groups, surface morphology, magnetic properties, and degree of porosity of the adsorbents, respectively. BET/BHJ technique confirmed the mesoporous nature of the compounds as their pore diameters ranged between 15 and 17 nm.

Perspectives and prospects of chelation extraction of heavy metals from wastewater: A review.

Heavy metals' contamination of water resources is a global environmental issue due to their detrimental effects on human health. To safeguard humans and the environment, toxic heavy metals must be removed from contaminated water because they cannot be broken down. Diverse technologies are employed to reduce the levels of heavy metals in wastewater.

Liquid-liquid extraction of copper(II), zinc(II), cadmium(II), and lead(II) from aqueous solution and sewage effluent using phenoxy-amino ligands.

The phenoxy-amino ligands 2-(((2-(diethylamino)ethyl)amino)methyl)phenol (L1) and 2-(((2-mercaptoethyl)amino)methyl)-phenol (L2) were studied as model chelating agents for liquid-liquid extraction of copper(II), zinc(II), cadmium(II), and lead(II) cations from water using dichloromethane-water biphasic system. The relative affinities of these chelating ligands for copper(II), zinc(II), cadmium(II), and lead(II) by liquid-liquid extraction were found to be in the order copper(II)> zinc(II) > cadmium(II) > lead(II). The ligands L1 and L2 showed binding efficiencies ranging from 78%-97% for copper(II), 75%-91% for zinc(II), 76%-92% for cadmium(II), and 59%-67% for lead(II).

Ethylene oligomerization studies by nickel(ii) complexes chelated by (amino)pyridine ligands: experimental and density functional theory studies.

Reductions of imine compounds 2-methoxy-N-(1-(pyridin-2-yl)ethylidene)ethanamine (L1), 2-methoxy-N-((pyridin-2-yl)methylene)ethanamine (L2), N,N-diethyl-N-((pyridin-2-yl)methylene)ethane-1,2-diamine (L3) and 2-((pyridin-2-yl)methyleneamino)ethanol (L4) using NABH4 produced their corresponding amine analogues N-(2-methoxyethyl)-1-(pyridin-2-yl)ethanamine (L1a), 2-methoxy-N-((pyridin-2-yl)methyl)-ethanamine (L2a), N,N-diethyl-N-((pyridin-2-yl)methyl)ethane-1,2-diamine (L3a) and 2-((pyridin-2-yl)methylamino)ethanol (L4a) in good yields. Reactions of the (amino)pyridine ligands L1a–L4a with [NiBr2(DME)] afforded nickel(II) complexes, [NiBr2(L1a)2] (1), [NiBr2(L2a)2] (2), [NiBr2(L3a)2] (3) and [NiBr2(L4a)2] (4), respectively in quantitative yields. Molecular structures of complexes 2 and 4 confirmed the formation of the bis(chelated)nickel(II) complexes.

Packing forces in dichloridobis(3,5-diphenyl-1H-pyrazole-κN(2))cobalt(II) dichloromethane hemisolvate.

The title compound, [CoCl2(C15H12N2)2]·0.5CH2Cl2, was crystallized from a binary mixture of dichloromethane and hexane and a dimeric supramolecular structure was isolated. The Co(II) centre exhibits a distorted tetrahedral geometry, with two independent pyrazole-based ligands occupying two coordination sites and two chloride ligands occupying the third and fourth coordination sites.