Cobalt(II), Zinc(II), Iron(III), and Copper(II) Complexes Bearing Positively Charged Quaternary Ammonium Functionalities: Synthesis, Characterization, Electrochemical Behavior, and SOD Activity
Autor: | Sabrina Sturm, Andrej Pevec, Dušanka Radanović, Iztok Turel, Mima Jevtović, Karsten Meyer, Matthias E. Miehlich, Ivana Ivanović-Burmazović, Andreas Scheitler, Katarina Andjelkovic, Božidar Čobeljić, Marko Stojičkov, Laura Senft |
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Rok vydání: | 2020 |
Předmět: |
Bearing (mechanical)
010405 organic chemistry Iron Structure elucidation chemistry.chemical_element Cobalt SOD activity Zinc 010402 general chemistry Electrochemistry 01 natural sciences Copper 0104 chemical sciences law.invention Characterization (materials science) Inorganic Chemistry chemistry.chemical_compound chemistry law ddc:540 Ammonium Nuclear chemistry |
Zdroj: | European Journal of Inorganic Chemistry |
ISSN: | 1099-0682 1434-1948 |
Popis: | We have synthesized and characterized Co(II) (1), Zn(II) (2), Fe(III) (3) and Cu(II) (4) complexes of 2,2'‐[2,6‐pyridinediylbis(ethylidyne‐1‐hydrazinyl‐2‐ylidene)]bis[N,N,N‐trimethyl‐2‐oxoethanaminium] dichloride (H2LCl2) by NMR, IR, and X‐Band EPR spectroscopy, respectively, as well as by single‐crystal X‐ray structural analysis. H2LCl2 belongs to the class of diacetylpyridine bis(hydrazone) ligands and bears two positively charged quaternary ammonium functionalities. The complexes 1–3 possess a pentagonal‐bipyramidal geometry, whereas 4 has square‐pyramidal geometry. Redox reactivity and SOD activity of the complexes was studied by means of electrochemical measurements in aqueous‐buffer and DMF or DMSO solutions, respectively, as well as by stopped‐flow measurements. Complexes 1–3 do not have SOD activity, whereas 4 exhibits a high catalytic rate constant for the superoxide dismutation, kcat = 1.73 × 107 m–1 s–1 (in MOPS buffer solution of pH = 7.4). The results were discussed in terms of complex redox potentials, electrostatic interactions and their spatial distribution, kinetic lability of metal centers, and stability of peroxo intermediates, respectively. |
Databáze: | OpenAIRE |
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