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Solubility, pseudoracemates

Figure 26 shows the ternary phase diagrams (solubility isotherms) for three types of solid solution. The solubilities of the pure enantiomers are equal to SA, and the solid-liquid equilibria are represented by the curves ArA. The point r represents the equilibrium for the pseudoracemate, R, whose solubility is equal to 2Sd. In Fig. 26a the pseudoracemate has the same solubility as the enantiomers, that is, 2Sd = SA, and the solubility curve AA is a straight line parallel to the base of the triangle. In Figs. 26b and c, the solid solutions including the pseudoracemate are, respectively, more and less soluble than the enantiomers. [Pg.377]

Fig. 26 Isothermal solubility diagrams of the three types of pseudoracemates (see text). The appearance of the tie lines is shown in the right half of the triangles. (Reproduced with permission of the copyright owner, John Wiley and Sons, Inc., New York, from Ref. 141, p. 197.)... Fig. 26 Isothermal solubility diagrams of the three types of pseudoracemates (see text). The appearance of the tie lines is shown in the right half of the triangles. (Reproduced with permission of the copyright owner, John Wiley and Sons, Inc., New York, from Ref. 141, p. 197.)...
The conglomerate shows a lower melting point (and hence, a higher solubility) than the individual enantiomers. From a melt or a solution with an enantiomeric ratio +1 1, the excess enantiomer crystallizes in pure form. The racemic compound may have a lower (curve 1) or a higher (curve 2) melting point (or solubility) than the corresponding enantiomers the eutectic mixture (E), however, always lies at a minimum. Finally, crystallization of pseudoracemates always yields enantiomerically impure samples. [Pg.77]

Less than 1% of racemic species are pseudoracemates, which show typical phase diagrams of continuous solid solutions. Figure 2c shows the three types of melting phase diagrams of pseudoracemates, which comprise ideal solid solutions, solid solutions with positive deviations from ideality, and solid solutions with negative deviations from ideality, respectively [13]. In real systems, the enantiomers and the racemic compound may display a small mutual solubility, even if they show eutectic behavior, which corresponds to terminal solid solutions for which the phase diagrams are shown in Figs. 2d and 2e. [Pg.21]

Figure 6 Ternary phase diagram showing the solubility of the racemic species (a) conglomerate, C, (b) racemic compound, R, (c) pseudoracemate, P i, ideal ii, positive deviations iii, negative deviations. D and L represent the enantiomers, S represents the solvent, at constant temperature. (From Ref. 10. Reproduced by permission of John Wiley and Sons.)... Figure 6 Ternary phase diagram showing the solubility of the racemic species (a) conglomerate, C, (b) racemic compound, R, (c) pseudoracemate, P i, ideal ii, positive deviations iii, negative deviations. D and L represent the enantiomers, S represents the solvent, at constant temperature. (From Ref. 10. Reproduced by permission of John Wiley and Sons.)...
Pseudoracemates may exhibit three types of ternary phase diagram, as mentioned previously (Fig. 6c). The change of solubility with composition is relatively small. Therefore we may expect similar solubilities and intrinsic dissolution rates for the enantiomer and the pseudoracemate. For the same reason, resolution of a pseudoracemate by crystallization is practically impossible [10]. [Pg.32]


See other pages where Solubility, pseudoracemates is mentioned: [Pg.379]    [Pg.379]    [Pg.435]    [Pg.332]    [Pg.1673]    [Pg.1675]    [Pg.1675]   
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