Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Oxidation of Thiols. IV. The Effect of Substituents on Ionization and Hexacyanoferrate (III) Oxidation of Monothiodiacylmethane
FAROUK H. AL-HAJJARAHMAD Y. KASSIM
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1979 年 27 巻 3 号 p. 620-624

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Ionization constants, pKa, for a set of six monothiodiacylmethanes have been determined in 50 vol% ethanol-water mixture at 25°±0.1. Excellent linear correlations are obtained when pKa values are plotted against the substituent constant, σx, and the polar substituent constant, σ*xC6H4, for substituted phenyl groups. The regression lines are : pKa=8.00-1.47 σx and pKa=8.92-1.195 σ*xC6H4, respectively. The pKa values are also correlated with the extended Hammett equation. The correlation follows the equation : pKa=7.717-1.330σI, x-1.248σR, x The rate of the oxidation of (Ie) with hexacyanoferrate (III) was discussed at different pH values.
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© The Pharmaceutical Society of Japan
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