PROTONATION EQUILIBRIA OF L-DOPA AND 1,10 PHENONTHROLINE IN PROPYLENE GLYCOL-WATER MIXTURES
Protonation equilibria of L-Dopa and 1,10 phenonthroline have been studied in varying concentrations (0-60% v/v) of propylene glycol-water mixtures maintaining an ionic strength of 0.16 mol dm-3 at 303 K using pH metric method. The protonation constants have been calculated with the computer program MINIQUAD75 and the best fit models are arrived at based on statistical grounds employing crystallographic R factor, χ2 , skewness and kurtosis. Dopa has three dissociable protons and one amino group which associate with proton. It exists as LH4+ at low pH and gets deprotonated with the formation of LH3, LH2- and LH2- successively with increase in pH. Phen forms LH2(2+) at low pH and gets deprotonated with the formation of LH+ and L with increase in pH. Secondary formation functions confirm the existence of 3 and 2 protonation equilibria for dopa and phen, respectively. The linear increase of log values of protonation constants of Dopa with decreasing dielectric constant of PG-water mixtures indicates the dominance of electrostatic forces in the protonation-deprotonation equilibria. Phen exhibits non-linear trend indicating the dominance of non-electrostatic forces.
| Main Authors: | , , , |
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| Format: | Digital revista |
| Language: | English |
| Published: |
Sociedad Chilena de Química
2011
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| Online Access: | http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072011000400004 |
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| Summary: | Protonation equilibria of L-Dopa and 1,10 phenonthroline have been studied in varying concentrations (0-60% v/v) of propylene glycol-water mixtures maintaining an ionic strength of 0.16 mol dm-3 at 303 K using pH metric method. The protonation constants have been calculated with the computer program MINIQUAD75 and the best fit models are arrived at based on statistical grounds employing crystallographic R factor, χ2 , skewness and kurtosis. Dopa has three dissociable protons and one amino group which associate with proton. It exists as LH4+ at low pH and gets deprotonated with the formation of LH3, LH2- and LH2- successively with increase in pH. Phen forms LH2(2+) at low pH and gets deprotonated with the formation of LH+ and L with increase in pH. Secondary formation functions confirm the existence of 3 and 2 protonation equilibria for dopa and phen, respectively. The linear increase of log values of protonation constants of Dopa with decreasing dielectric constant of PG-water mixtures indicates the dominance of electrostatic forces in the protonation-deprotonation equilibria. Phen exhibits non-linear trend indicating the dominance of non-electrostatic forces. |
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