协同溶剂化能提高水以外的极性吗?1,2-二甲氧基乙烷,2-甲氧基乙醇和乙二醇的二元水混合物的有趣案例研究。

IF 3.2 2区 化学 Q3 CHEMISTRY, PHYSICAL The Journal of Physical Chemistry B Pub Date : 2025-02-20 Epub Date: 2025-02-05 DOI:10.1021/acs.jpcb.4c07433
Puspal Mukherjee, Sanchaita Das, Deblina Mallick, Sanjay Roy, Sintu Ganai
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引用次数: 0

摘要

本研究采用香豆素461 (C461)、4-氨苯酰亚胺(4AP)和对硝基苯胺(pNA)三种溶剂致变色染料,通过稳态紫外可见光谱和荧光发射光谱研究了1,2-二甲氧基乙烷(DME)、2-甲氧基乙醇(2ME)和乙二醇(EG)二元水相混合物的增效行为。染料的吸收最大值随溶剂混合物组成的变化而发生广泛的色移。在混合物的富水区,与纯水区相比,吸收最大值显示出明显更大的色移。观察到一个明显的协同溶剂化现象,表明混合物的极性超过纯水的极性。水-二甲醚和水-二甲醚的协同作用明显,而水-乙醚的协同作用较弱。这种“超极性”是用广义博世溶剂化模型从摩尔跃迁能的变化来分析的。在水-二甲醚和水-二甲醚混合物中,协同溶剂化的平衡常数显著大于优先溶剂化的平衡常数,而在水-乙醚混合物中,这两个值是相当的。这种行为源于水和共溶剂之间的分子间氢键。协同溶剂化的摩尔分数表明混合物中溶质周围存在微观非均质性。值得注意的是,探针的发射最大值的变化没有显示出协同行为,这意味着溶剂在激发态的重定向破坏了协同效应。红外光谱还对二元混合物中的氢键结构进行了研究。建立了-OH和-CH拉伸频率的分析模型,揭示了水-二甲醚和水-二甲醚氢键聚集体的形成是观察到的协同“超极性”效应的原因。
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Can Synergistic Solvation Increase Polarity Beyond Water? An Intriguing Case Study of Aqueous Binary Mixtures of 1,2-Dimethoxyethane, 2-Methoxyethanol, and Ethylene Glycol.

In this study, the synergistic behavior of aqueous binary mixtures of 1,2-dimethoxyethane (DME), 2-methoxyethanol (2ME), and ethylene glycol (EG) was investigated using three solvatochromic dyes: coumarin 461 (C461), 4-aminophthalimide (4AP), and para-nitroaniline (pNA) through steady-state UV-visible spectroscopy and fluorescence emission spectroscopy. The absorption maxima of the dyes exhibited extensive bathochromic shifts with varying solvent mixture compositions. In the water-rich region of the mixtures, the absorption maxima displayed significantly larger bathochromic shifts compared with those in pure water. A clear case of synergistic solvation was observed, indicating that the polarity of mixtures exceeds that of pure water. The synergistic effect was pronounced in the water-DME and water-2ME mixtures, while it was weaker in the water-EG mixture. This "hyper-polarity" was analyzed from the molar transition energy variation using a generalized Bosch solvation model. In the water-DME and water-2ME mixtures, the equilibrium constant for synergistic solvation was significantly greater than that for preferential solvation, whereas in the water-EG mixture, the values were comparable. This behavior stemmed from the intermolecular hydrogen bonding between water and cosolvents. The mole fraction of synergistic solvation suggested microheterogeneity around the solute within the mixtures. Notably, the variation in emission maxima of the probes showed no synergistic behavior, implying that solvent reorientation in the excited state disrupts the synergistic effect. IR spectroscopy was also employed to investigate the hydrogen-bonded structures in the binary mixtures. Analytical modeling of -OH and -CH stretching frequency was established, and it revealed that the formation of water-DME and water-2ME hydrogen-bonded aggregates is responsible for the observed synergistic "hyper-polarity" effect.

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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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