School of Chemical Sciences, North Maharashtra University , Jalgaon-425001, India.
J Phys Chem B. 2013 Dec 19;117(50):16249-59. doi: 10.1021/jp410814w. Epub 2013 Nov 26.
The osmotic coefficient measurements for binary aqueous solutions of 2,2,2-cryptand (4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8] hexacosane) in the concentration range of 0.009 to ~0.24 mol·kg(-1) and in ternary aqueous solutions containing a fixed concentration of 2,2,2-cryptand of ~0.1 mol·kg(-1) with varying concentration of KBr (0.06 to ~0.16 mol·kg(-1)) have been reported at 298.15 K. The diamine gets hydrolyzed in aqueous solutions and needs proper approach to obtain meaningful thermodynamic properties. The measured osmotic coefficient values are corrected for hydrolysis and are used to determine the solvent activity and mean ionic activity coefficients of solute as a function of concentration. Strong ion-pair formation is observed, and the ion-pair dissociation constant for the species CrptH[OH(-)] is reported. The excess and mixing thermodynamic properties (Gibbs free energy, enthalpy, and entropy changes) have been obtained using the activity data from this study and the heat data reported in the literature. Further, the data are utilized to compute the partial molal entropies of solvent and solute at finite as well as infinite dilution of 2,2,2-cryptand in water. The concentration dependent non-linear enthalpy-entropy compensation effect has been observed for the studied system, and the compensation temperature along with entropic parameter are reported. Using solute activity coefficient data in ternary solutions, the transfer Gibbs free energies for transfer of the cryptand from water to aqueous KBr as well as transfer of KBr from water to aqueous cryptand were obtained and utilized to obtain the salting constant (ks) and thermodynamic equilibrium constant (log K) values for the complex (2,2,2-cryptand:K(+)) at 298.15 K. The value of log K = 5.8 ± 0.1 obtained in this work is found to be in good agreement with that reported by Lehn and Sauvage. The standard molar entropy for complexation is also estimated for the 2,2,2-cryptand-KBr complex in aqueous medium.
在 298.15 K 下,报道了 2,2,2-穴醚(4,7,13,16,21,24-六氧-1,10-二氮杂双环[8.8.8]二十六烷)在浓度范围约 0.009 至 0.24 mol·kg(-1) 的二元水溶液以及含有固定浓度约 0.1 mol·kg(-1) 2,2,2-穴醚的三元水溶液中的渗透系数测量值,其中溴化钾的浓度变化约 0.06 至 0.16 mol·kg(-1)。二胺在水溶液中会发生水解,需要采用适当的方法来获得有意义的热力学性质。测量的渗透系数值经过水解校正后,用于确定溶剂活度和溶质的平均离子活度系数随浓度的变化。观察到强离子对的形成,并报告了物种 CrptH[OH(-)]的离子对离解常数。使用该研究中的活度数据和文献中报道的热数据,获得了超额和混合热力学性质(吉布斯自由能、焓和熵变化)。此外,还利用这些数据计算了在有限和无限稀释条件下 2,2,2-穴醚在水中的溶剂和溶质的偏摩尔熵。观察到所研究体系的浓度相关非线性焓熵补偿效应,并报告了补偿温度和熵参数。使用三元溶液中的溶质活度系数数据,获得了穴醚从水到水合溴化钾以及溴化钾从水到水合穴醚的转移吉布斯自由能,并利用这些数据获得了穴醚从水到水合溴化钾以及溴化钾从水到水合穴醚的盐化常数 (ks) 和热力学平衡常数 (log K) 值,该值在 298.15 K 下。本工作得到的 log K = 5.8 ± 0.1 值与 Lehn 和 Sauvage 报道的值吻合较好。还估计了 2,2,2-穴醚-溴化钾配合物在水介质中的标准摩尔熵。