In this study, dispersive liquid-liquid microextraction method was used for the preconcentration and simultaneous determination of Co(II) and Fe(III) in water samples as their oxinate chelates. In dispersive liquid-liquid microextraction process, methanol and chloroform were used as disperser and extracting solvents, respectively, and the ligand 8-hydroxy quinoline was used as a chelating agent for the extraction of Co(II) and Fe(III). HPLC was applied for the quantitation of the analytes after preconcentration. An experimental design, central composite design, coupled with response surface methodology was used for the optimization of the involved experimental parameters. In addition, the effect of various experimental parameters in the extraction was investigated using one variable at a time method. The calibration graphs were linear in the range of 20-4000 microg/L with the LODs of 3 microg/L for both analytes. The RSDs for six replicate measurements of 500 microg/L of Co(2+) and Fe(3+) were 3.3 and 4.1%, respectively.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/jssc.200900460 | DOI Listing |
Chem Sci
December 2024
Jagiellonian University, Faculty of Chemistry Gronostajowa 2 30-387 Kraków Poland +48 12 686 24 89.
Chem Biodivers
November 2024
Department of Chemistry, Faculty of Science, Sohag University, Sohag, Egypt.
Int J Health Sci (Qassim)
January 2024
Department of Clinical Laboratory Sciences, College of Applied Medical Science, Jouf University, Aljouf, Saudi Arabia.
Chempluschem
September 2024
Institut de Ciència Molecular (ICMol), Universitat de València, Catedrático José Beltrán 2, 46980, Paterna, Spain.
The synthesis and characterization of a Co/Fe mixed-metal banana-shaped polyoxometalate with the formula [(CoFe(HO)PWO)(PWO)] (CoFe) is reported. This transition-metal-substituted polyoxometalate readily assembles from its components in a one-pot reaction and crystallizes in the monoclinic space group P2/c. The structure of CoFe can be considered a double sandwich composed by two B-α-{CoFePWO} Keggin units, in which one coordinatively saturated octahedral metal position is equally occupied by Co(II) and Fe(III) ions with a 50 % of site occupancy.
View Article and Find Full Text PDFPhys Chem Chem Phys
October 2024
State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Why does binding of dioxygen (O) to metal centers, the initial step of O storage, transportation, and activation, almost inevitably induce metal-to-O single-electron transfer and generate superoxo (O˙) species, instead of genuine O02 adducts? To address this question, this study describes highly correlated wavefunction-based calculations using CASSCF/NEVPT2 (CASSCF = complete active space self-consistent field, and NEVPT2 = -electron valence state second-order perturbation theory) approaches to explore the electronic-structure evolution of O association on Fe(II)(BDPP) (HBDPP = 2,6-bis((2-()-diphenylhydroxylmethyl-1-pyrrolidinyl)methyl)pyridine) and Co(II)(BDPP) to produce = 3 Fe(III)(BDPP)(O˙) (1) and Co(III)(BDPP)(O˙) (2). CASSCF/NEVPT2 calculations suggest that the processes furnishing 1 and 2 feature an avoided crossing resulting from interactions of two diabatic curves, of which one is characterized as Co(II) and Fe(II) centers interacting with a triplet O ligand and the other as Co(III) and Fe(III) centers bound to a superoxo ligand. In both cases, the avoided crossing induces a one-electron transfer from the divalent metal center to the incoming O ligand and leads to formation of trivalent metal-O˙ complexes.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!