Department of Chemistry, Indian Institute of Technology, Guwahati 781039, Assam, India.
J Chem Phys. 2013 Nov 21;139(19):194504. doi: 10.1063/1.4830414.
The effect of salt concentration on association properties of caffeine molecule was investigated by employing molecular dynamics simulations in isothermal-isobaric ensemble of eight caffeine molecules in pure water and three different salt (NaCl) concentrations, at 300 K temperature and 1 atm pressure. The concentration of caffeine was taken almost at the solubility limit. With increasing salt concentration, we observe enhancement of first peak height and appearance of a second peak in the caffeine-caffeine distribution function. Furthermore, our calculated solvent accessible area values and cluster structure analyses suggest formation of higher order caffeine cluster on addition of salt. The calculated hydrogen bond properties reveal that there is a modest decrease in the average number of water-caffeine hydrogen bonds on addition of NaCl salt. Also observed are: (i) decrease in probability of salt contact ion pair as well as decrease in the solvent separated ion pair formation with increasing salt concentration, (ii) a modest second shell collapse in the water structure, and (iii) dehydration of hydrophobic atomic sites of caffeine on addition of NaCl.
采用等压等温热力学系综,在 300 K 温度和 1 大气压压力下,对 8 个咖啡因分子在纯水中和 3 种不同盐(NaCl)浓度下的咖啡因分子缔合特性进行了研究。咖啡因的浓度几乎达到了溶解度极限。随着盐浓度的增加,我们观察到咖啡因-咖啡因分布函数的第一峰值高度增加,并出现第二个峰值。此外,我们计算的溶剂可及面积值和簇结构分析表明,在添加盐时形成了更高阶的咖啡因簇。计算得到的氢键性质表明,在添加 NaCl 盐时,水-咖啡因氢键的平均数量略有减少。还观察到:(i)随着盐浓度的增加,盐接触离子对的概率以及溶剂分离离子对的形成减少;(ii)在水中结构中第二壳层适度塌陷;(iii)在添加 NaCl 时,咖啡因的疏水性原子位点脱水。