Distribution, between solvents

Oxytocin [50-56-6] M 1007.2, m dec on heating, [a] -26.2"(c 0.53, N AcOH). A cyclic nonapeptide which was purified by countercurrent distribution between solvent and buffer. It is soluble in H2O, rt-BuOH and isoBuOH. [Bodanszky and du Vigneaud J Am Chem Soc 81 2504 1959 Cash et al. J Med Pharm Chem 5 413 1962 Sakakibara et al. Bull Chem Soc Jpn 38 120 1965 solid phase synthesis Bayer and... 

The most popular method for measuring the polarity of a solute entails determination of the distribution constant between water and a water-immiscible solvent, e.g., octanol. However, because there is difficulty in dissolving proteins in the solvent, a two-phase aqueous system was developed (Shanbhag and Axelson, 1975). Albertson (1986) reported the construction of various aqueous phase systems for partitioning proteins, other macromolecules, and even cells. Recently, simpler aqueous biphase systems were selected for hydrophobic partitioning of proteins (Hachem et al., 1996). However, because of restrictions similar to those for HIC, as discussed above, it may be premature to replace the method used in Basic Protocol 5. The definition of hydrophobicity is based on the polarity of chemical compounds, which is closely related to the distribution between solvents of different polarities. This theory is similar to the elution mechanism of phase distribution chromatography as well as phase partition. However, complexity in the partition system and procedure hampers the broad use of the phase partition approaches. 

Figure 13. Acid distribution between solvent and feed solvent = 30 vol % DBBP-70 vol % Isopar H, T = 21 °C organic. aqueous = 1 1...

Kishino, T. and Kobayashi, K. 1980. A study on the absorption mechanism of pentachlorophenol in goldfish relating to its distribution between solvents and water. Bull. Jap. Soc. Sci. Fish. 46 1165-1168. 

The stabiHty criteria for ternary and more complex systems may be obtained from a detailed analysis involving chemical potentials (23). The activity of each component is the same in the two Hquid phases at equiHbrium, but in general the equiHbrium mole fractions are greatiy different because of the different activity coefficients. The distribution coefficient m based on mole fractions, of a consolute component C between solvents B and A can thus be expressed... 

Liquid-liquid extraction is a process for separating components in solution by their distribution between two immiscible liquid phases. Such a process can also be simply referred to as liquid extraction or solvent extraction however, the latter term may be confusing because it also applies to the leaching of a soluble substance from a solid. 

The Self-Consistent Reaction Field (SCRF) model considers the solvent as a uniform polarizable medium with a dielectric constant of s, with the solute M placed in a suitable shaped hole in the medium. Creation of a cavity in the medium costs energy, i.e. this is a destabilization, while dispersion interactions between the solvent and solute add a stabilization (this is roughly the van der Waals energy between solvent and solute). The electric charge distribution of M will furthermore polarize the medium (induce charge moments), which in turn acts back on the molecule, thereby producing an electrostatic stabilization. The solvation (free) energy may thus be written as... 

The distribution coefficient for n-heptane (solute i) distributed between ethylene glycol (solvent 1) and benzene (solvent 2) at 25°C is given as the ratio of mass fractions... 

It was also found experimentally that two solutes were distributed between a pair of solvents as if each were present. alone. (This is analogous to Dalton s law of partial pressures.)... 

We assume that an equilibrium can subsist with a specified pair of solvents in contact and a solute distributed between them in any one ratio of concentrations ... 

If an electrolyte AB is distributed between two solvents, a and f3, there will in general be a difference of potential established across the boundary, due to the existence of a double layer ( 198). 

The isopiestic method is based upon the equality of the solvent chemical potentials and fugacities when solutions of different solutes, but the same solvent, are allowed to come to equilibrium together. A method in which a solute is allowed to establish an equilibrium distribution between two solvents has also been developed to determine activities of the solute, usually based on the Henry s law standard state. In this case, one brings together two immiscible solvents, A and B, adds a solute, and shakes the mixture to obtain two phases that are in equilibrium, a solution of the solute in A with composition. vA, and a solution of the solute in B with composition, a . 

At infinite dilution, 1-pentanol monomers distribute between AOT-reversed micelles and the continuous organic phase, whereas at finite alcohol concentration, given the ability of alcohol to self-assemble in the apolar organic solvent, a coexistence between reversed micelles (solubilizing 1-pentanol) and alcoholic aggregates (incorporating AOT molecules) is realized [25],... 

Figure 11.56. Equilibrium diagram solute distributed between two solvents...

Solvent extraction, sometimes called liquid-liquid extraction, involves the selective transfer of a substance from one liquid phase to another. Usually, an aqueous solution of the sample is extracted with an immiscible organic solvent. For example, if an aqueous solution of iodine and sodium chloride is shaken with carbon tetrachloride, and the liquids allowed to separate, most of the iodine will be transferred to the carbon tetrachloride layer, whilst the sodium chloride will remain in the aqueous layer. The extraction of a solute in this manner is governed by the Nernstpartition or distribution law which states that at equilibrium, a given solute will always be distributed between two essentially immiscible liquids in the same proportions. Thus, for solute A distributing between an aqueous and an organic solvent,... 

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