Cation Effects on Rotational Dynamics of Anions and Water Molecules in Alkali (Li+, Na+, K+, Cs+) Thiocyanate (SCN-) Aqueous Solutions

被引:66
|
作者
Bian, Hongtao [1 ]
Chen, Hailong [1 ]
Zhang, Qiang [2 ]
Li, Jiebo [1 ]
Wen, Xiewen [1 ]
Zhuang, Wei [2 ]
Zheng, Junrong [1 ]
机构
[1] Rice Univ, Dept Chem, Houston, TX 77005 USA
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Mol React Dynam, Dalian 116023, Liaoning, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2013年 / 117卷 / 26期
关键词
VIBRATIONAL-ENERGY TRANSFER; HYDROGEN-BOND STRUCTURE; LIQUID WATER; MOLTEN THIOCYANATES; HOFMEISTER SERIES; PHASE-TRANSITION; SALT-SOLUTIONS; RAMAN-SPECTRA; IONS; HYDRATION;
D O I
10.1021/jp4016646
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Waiting time dependent rotational anisotropies of SCN- anions and water molecules in alkali thiocyanate (XSCN, X = Li, Na, K, Cs) aqueous solutions at various concentrations were measured with ultrafast infrared spectroscopy. It was found that cations can significantly affect the reorientational motions of both water molecules and SCN- anions. The dynamics are slower in a solution with a smaller cation. The reorientational time constants follow the order of Li+ > Na+ > K+ similar or equal to Cs+. The changes of rotational time constants of SCN- at various concentrations scale almost linearly with the changes of solution viscosity, but those of water molecules do not. In addition, the concentration-dependent amplitudes of dynamical changes are much more significant in the Li+ and Na+ solutions than those in the K+ and Cs+ solutions. Further investigations on the systems with the ultrafast vibrational energy exchange method and molecular dynamics simulations provide an explanation for the observations: the observed rotational dynamics are the balanced results of ion clustering and cation/anion/water direct interactions. In all the solutions at high concentrations (>5 M), substantial amounts of ions form clusters. The structural inhomogeneity in the solutions leads to distinct rotational dynamics of water and anions. The strong interactions of Li+ and Na+ because of their relatively large charge densities with water molecules and SCN- anions, in addition to the likely geometric confinements because of ion clustering, substantially slow down the rotations of SCN- anions and water molecules inside the ion clusters. The interactions of K+ and Cs+ with water or SCN- are much weaker. The rotations of water molecules inside ion clusters of K+ and Cs+ solutions are not significantly different from those of other water species so that the experimentally observed rotational relaxation dynamics are only slightly affected by the ion concentrations.
引用
收藏
页码:7972 / 7984
页数:13
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