Wu Xiangen, Lu Wanjun, Streacker Louis M, Ashbaugh Henry S, Ben-Amotz Dor
College of Marine Science and Technology, China University of Geosciences, Wuhan, 430074, China.
State Key Laboratory of Geological Processes and Mineral Resources, China University of Geosciences, Wuhan, 430074, China.
Angew Chem Int Ed Engl. 2018 Nov 12;57(46):15133-15137. doi: 10.1002/anie.201809372. Epub 2018 Oct 18.
The influence of oily molecules on the structure of liquid water is a question of importance to biology and geology and many other fields. Previous experimental, theoretical, and simulation studies of methane in liquid water have reached widely conflicting conclusions regarding the structure of hydrophobic hydration-shells. Herein we address this question by performing Raman hydration-shell vibrational spectroscopic measurements of methane in liquid water from -10 °C to 300 °C (at 30 MPa, along a path that parallels the liquid-vapor coexistence curve). We show that, near ambient temperatures, methane's hydration-shell is slightly more tetrahedral than pure water. Moreover, the hydration-shell undergoes a crossover to a more disordered structure above ca. 85 °C. Comparisons with the crossover temperature of aqueous methanol (and other alcohols) reveal the stabilizing influence of an alcohol OH head-group on hydrophobic hydration-shell fragility.
油性分子对液态水结构的影响是一个对生物学、地质学及许多其他领域都很重要的问题。此前关于液态水中甲烷的实验、理论和模拟研究,在疏水水化层结构方面得出了广泛冲突的结论。在此,我们通过对-10°C至300°C(在30MPa下,沿一条与液-气共存曲线平行的路径)液态水中的甲烷进行拉曼水化层振动光谱测量来解决这个问题。我们表明,在接近环境温度时,甲烷的水化层比纯水略微更呈四面体结构。此外,水化层在约85°C以上转变为更无序的结构。与甲醇水溶液(及其他醇类)的转变温度进行比较,揭示了醇类OH头基对疏水水化层脆性的稳定作用。