Sequestration of Hg2+ by Some Biologically Important Thiols
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文摘
A potentiometric and 1H NMR investigation on the interactions between Hg2+ and some biologically important sulfhydryl ligands, such as cysteine (H2CYS), penicillamine (H2PSH), and glutathione (H3GSH), is reported. Equilibria were studied at T = 298.15 K, in the ionic strength range (0.1 to 1) mol路kg鈥?, using as ionic medium NaCl in the presence of iodide (NaI) as a competitive ligand. Results show the formation of HgL2鈥?i>z, HgLH3鈥?i>z, HgLH24鈥?i>z, HgL22鈥?z, HgL2H3鈥?z, and HgL2H24鈥?z species (Lz鈥?/sup> = CYS2鈥?/sup>, PSH2鈥?/sup>, or GSH3鈥?/sup>) together with HgL2H3鈥?/sup> for GSH3鈥?/sup> only. Formation constant values are very high with, as an example, log 尾 = 34.54, 34.24, and 32.05 for Hg(CYS)0, Hg(PSH)0, and Hg(GSH)鈭?/sup> species, respectively (at I = 0.25 mol路kg鈥?, T = 298.15 K). 1H NMR measurements at I = 0.25 mol路kg鈥? (NaCl) fully confirm the potentiometric findings. The speciation diagrams show that most of the metal fraction is present as complex species in a wide pH range, and the hydrolysis of the cation is completely suppressed. The sequestering ability of ligands toward Hg2+ is very high, and it was analyzed and compared at different pH and ionic strengths.

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