Influence of CTAB Reverse Micellar Confinement on the Tetrahedral Structure of Liquid Water.

IF 2.8 2区 化学 Q3 CHEMISTRY, PHYSICAL
Anupama Sharma, Mywish Anand, Sudip Chakraborty
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Abstract

The effect of confinement on the tetrahedral ordering of liquid water plays a vital role in controlling their microscopic structure and dynamics as well as their spectroscopic properties. In this article, we have performed the classical molecular dynamics simulations of four different CTAB/water/chloroform reverse micelles with varied water content to study how the tetrahedral ordering of nanoscale water inside reverse micellar confinement influences the microscopic dynamics and the structural relaxation of water···water hydrogen bonds and its impact on the low-frequency intermolecular vibrational bands. We have noticed from the results obtained from simulated trajectories the lowering trends of tetrahedral ordering of water pools in reverse micellar confinements as we move from bulk to confined and strictly confined environments. We have observed that the order of confinements significantly altered the relaxation pattern of water···water hydrogen bonds present in the nanoscale water pool of reverse micelles. The recrossing related to hydrogen bond dynamics can effectively explain the relaxation pattern of CHBWW(t) under confinement. The Br-1···water hydrogen bond depicts a much slower relaxation compared to the water···water hydrogen bonds inside reverse micelles. We have also explored the correlation between the tetrahedral ordering of nanoscale water pools and the relaxation of water···water hydrogen bonds with the 50 cm-1 band for water inside reverse micelles. The computations reported that compared to bulk water, the band appearing at 50 cm-1 for O···O···O triplet bending is nonuniformly blue-shifted by 18-45 cm-1 for the nanoscale water pool inside reverse micelles, and the intensity of the band drops from bulk to confined and strictly confined environments, which indicates the reduced tendency of such triplet formation. It is observed that a significant intensity variation at the 200 cm-1 band correlates with the effect of confinement on the tetrahedral ordering of the water pool inside reverse micelles. So, our observations support the influence of strictly confined environments on the tetrahedral water structure to adopt the quasi-two-dimensional water network and experience restricted longitudinal translations. It is further noticed that the 500 cm-1 librational band is also found to be blue-shifted by 71-112 cm-1 for the water pool in reverse micelles, and the extent of the shift being more noticeable for strictly confined environments correlates excellently with the sluggish relaxation of water···water hydrogen bonds in such environments.

CTAB反胶束约束对液态水四面体结构的影响。
约束对液态水四面体有序的影响,对控制液态水的微观结构、动力学和光谱性质起着至关重要的作用。本文对四种不同含水量的CTAB/水/氯仿反胶束进行了经典分子动力学模拟,研究了纳米尺度水在反胶束约束下的四面体排列顺序对水···水氢键微观动力学和结构弛弛性的影响及其对分子间低频振动带的影响。从模拟轨迹得到的结果中,我们注意到,当我们从散装环境移动到密闭和严格密闭环境时,反胶束约束中水池的四面体有序度呈下降趋势。我们观察到束缚的顺序显著改变了反胶束纳米水池中水···水氢键的弛豫模式。与氢键动力学相关的重交可以有效地解释约束下CHBWW(t)的弛缓模式。Br-1···水氢键的弛豫速度比逆胶束中的水···水氢键慢得多。我们还探索了纳米尺度水池的四面体有序与水···水氢键在反胶束内50 cm-1带弛豫的关系。计算结果表明,与体积水相比,反胶束内的纳米级水池在50 cm-1处出现的O··O·O三重态弯曲带不均匀蓝移了18-45 cm-1,并且从体积环境到密闭环境和严格密闭环境的波段强度下降,表明这种三重态形成的趋势减少。观察到,在200 cm-1波段上的显著强度变化与约束对反胶束内水池四面体有序度的影响有关。因此,我们的观测结果支持严格限制环境对四面体水结构的影响,采用准二维水网络,并经历有限的纵向平移。在反胶束中,水体的500 cm-1振动带也发生了71 ~ 112 cm-1的蓝移,在严格限制的环境中,这种蓝移的程度更为明显,这与这种环境中水···水氢键的缓慢松弛有很好的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.80
自引率
9.10%
发文量
965
审稿时长
1.6 months
期刊介绍: An essential criterion for acceptance of research articles in the journal is that they provide new physical insight. Please refer to the New Physical Insights virtual issue on what constitutes new physical insight. Manuscripts that are essentially reporting data or applications of data are, in general, not suitable for publication in JPC B.
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