Equilibrium studies of 5-substituted 4-hydroxy-2-methylpyrimidines. III. Photometric titration in n-butanol.
TAKAYASU KITAGAWA
Abstract
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TAKAYASU KITAGAWA
Abstract
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Photometric titration for 5-substituted 4-hydroxy-2-methylpyrimidine and its methyl derivatives was performed in n-BuOH. An equation for the titration was derived in consideration of ion pair formation in n-BuOH. [numerical formula] It was proved that Higuchi's Type II plot method was applicable only under a condition, KBHX=KIHX, from the analysis of the titration curves. The over-all dissociation constant of the pyrimidines (Kn-BuOHBH=KOHX/KBKBHX=[H+] [B]fH/[BH+] fBH) was estimated from the slope of the titration curve. The basicities of the compounds in n-BuOH generally increased as compared with those in water (ΔpK=pKn-BuOHBH-pKa=-0.1-2.3). The degrees of the increase differed largely among the compounds. Much larger increase of the basicity than the other compounds (ΔpK ; 2.1-2.3) was found for 5-substituted 1, 2-dimethyl-4(1H)-pyrimidones.
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Photometric titration for 5-substituted 4-hydroxy-2-methylpyrimidine and its methyl derivatives was performed in n-BuOH. An equation for the titration was derived in consideration of ion pair formation in n-BuOH. [numerical formula] It was proved that Higuchi's Type II plot method was applicable only under a condition, KBHX=KIHX, from the analysis of the titration curves. The over-all dissociation constant of the pyrimidines (Kn-BuOHBH=KOHX/KBKBHX=[H+] [B]fH/[BH+] fBH) was estimated from the slope of the titration curve. The basicities of the compounds in n-BuOH generally increased as compared with those in water (ΔpK=pKn-BuOHBH-pKa=-0.1-2.3). The degrees of the increase differed largely among the compounds. Much larger increase of the basicity than the other compounds (ΔpK ; 2.1-2.3) was found for 5-substituted 1, 2-dimethyl-4(1H)-pyrimidones.
Key concepts: Titration, Chemistry, Dissociation constant, Titration curve, Dissociation (chemistry), Butanol, Analytical Chemistry (journal), Physical chemistry