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- W2004125971 endingPage "1742" @default.
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- W2004125971 abstract "Standard potentials of I3−/I− and I2/I3− redox couples relative to that of aqueous saturated calomel reference electrode SCE (W), ESCE(w) have been determined in propylene carbonate (PC), N,N-dimethylformamide (DMF), acetonitrile (ACN), and their binary mixtures at 25 °C from potentiometric measurements. The results helped evaluate the standard potentials of the redox couple I2/I− relative to ESCE(w) as well as the related formation constant (Kf) of I3− in these solvent systems. The solvent effects on the formation equilibrium I2+I−ightleftharpoonsI3− were analyzed in the light of the transfer free energies of I2, ΔGt°(I2), as obtained from solubility measurements of I2 in the solvents, that of I−, ΔGt°(I−), as obtained earlier by use of the widely used TATB reference electrolyte assumption and that of I3−, ΔGt°(I3−), as obtained by subtracting these two contributions from the respective transfer free energies of formation equilibrium in the mixed solvents relative to a chosen reference solvent in each solvent system. The solvation behavior of these individual iodine species viz. I2, I−, I3− was interpreted in terms of involved interaction viz. Born, ion-dipole, ion-induced dipole, dispersion type soft–soft interactions, CTTS complexation and also the cavity effect as computed by the scaled particle theory (SPT)." @default.
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- W2004125971 date "1988-05-01" @default.
- W2004125971 modified "2023-09-24" @default.
- W2004125971 title "Relative Standard Electrode Potentials of I<sub>3</sub><sup>−</sup>/I<sup>−</sup>, I<sub>2</sub>/I<sub>3</sub><sup>−</sup>, and I<sub>2</sub>/I<sup>−</sup>Redox Couples and the Related Formation Constants of I<sub>3</sub><sup>−</sup>in Some Pure and Mixed Dipolar Aprotic Solvents" @default.
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- W2004125971 doi "https://doi.org/10.1246/bcsj.61.1735" @default.
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