Shimizu Seishi, Matubayasi Nobuyuki
York Structural Biology Laboratory, Department of Chemistry, University of York, Heslington, York YO10 5DD, UK.
Phys Chem Chem Phys. 2017 Oct 11;19(39):26734-26742. doi: 10.1039/c7cp04990k.
Solubilization or mixing in the presence of hydrotropes is often accompanied by the increase of scattering intensity. When the scattering corresponding to mesoscale structuring grows, the mixed state is called the "pre-ouzo" aggregate, which appears often and is distinct from critical density fluctuation, yet its precise mechanism of appearance is still obscure. Combining the results from the theories of scattering and thermodynamic phase stability with differential geometry, we have constructed a theory which can account for hydrotrope mixing thermodynamics and the pre-ouzo effect in a unified manner. In addition, another well-known signature of hydrotropy, the minimum hydrotrope concentration (MHC) at which solubility of sparingly soluble hydrophobic solutes suddenly increases, has also been linked to the scattering increase. The thermodynamic signatures of the pre-ouzo effect and MHC reveal a mechanistic difference between them, which manifests in the thermodynamic order of derivatives.
在助溶试剂存在的情况下进行增溶或混合时,散射强度通常会增加。当中尺度结构对应的散射增强时,混合态被称为“前乌佐”聚集体,这种聚集体经常出现且与临界密度涨落不同,但其确切的出现机制仍不清楚。我们将散射理论、热力学相稳定性理论的结果与微分几何相结合,构建了一种能够统一解释助溶试剂混合热力学和前乌佐效应的理论。此外,助溶作用的另一个著名特征,即难溶性疏水溶质溶解度突然增加时的最低助溶试剂浓度(MHC),也与散射增加有关。前乌佐效应和MHC的热力学特征揭示了它们之间的机制差异,这体现在导数的热力学顺序上。