Verma Pramod Kumar, Kundu Achintya, Puretz Matthew S, Dhoonmoon Charvanaa, Chegwidden Oriana S, Londergan Casey H, Cho Minhaeng
Center for Molecular Spectroscopy and Dynamics, Institute for Basic Science (IBS), Department of Chemistry , Korea University , Seoul 02841 , Republic of Korea.
Department of Chemistry , Haverford College , 370 Lancaster Avenue , Haverford , Pennsylvania 19041 , United States.
J Phys Chem B. 2018 Mar 8;122(9):2587-2599. doi: 10.1021/acs.jpcb.7b09641. Epub 2017 Nov 27.
Water is an extensively self-associated liquid due to its extensive hydrogen bond (H-bond) forming ability. The resulting H-bonded network fluid exhibits nearly continuous absorption of light from the terahertz to the near-IR region. The relatively weak bend+libration water combination band (centered at 2130 cm) has been largely overlooked as a reporter of liquid water's structure and dynamics despite its location in a convenient region of the IR for spectroscopic study. The intermolecular nature of the combination band leads to a unique absorption signal that reports collectively on the rigidity of the H-bonding network in the presence of many different solutes. This study reports comprehensively how the combination band acts as an intrinsic and collective probe in various chemically and biologically relevant solutions, including salts of varying character, denaturants, osmolytes, crowders, and surfactants that form reverse micelles and micelles. While we remark on changes in the line width and intensity of this combination band, we mainly focus on the frequency and how the frequency reports on the collective H-bonding network of liquid water. We also comment on the "association band" moniker often applied to this band and how to evaluate discrete features in this spectral region that sometimes appear in the IR spectra of specific kinds of aqueous samples of organic solutes, especially those with very high solute concentrations, with the conclusion that most of these discrete spectral features come exclusively from the solutes and do not report on the water. Contrasts are drawn throughout this work between the collective and delocalized reporting ability of the combination band and the response of more site-specific vibrations like the much-investigated OD stretch of HDO in HO: the combination band is a unique reporter of H-bonding structure and dynamics and fundamentally different than any local mode probe. Since this band appears as the spectroscopic "background" for many local-mode reporter groups, we note the possibility of observing both local and collective solvent dynamics at the same time in this spectral region.
由于水具有广泛形成氢键(H键)的能力,它是一种广泛自缔合的液体。由此产生的氢键网络流体在太赫兹到近红外区域表现出几乎连续的光吸收。尽管位于红外光谱研究的便利区域,但相对较弱的弯曲+摆动水组合带(中心位于2130 cm)在很大程度上被忽视,未能作为液态水结构和动力学的报告者。该组合带的分子间性质导致了一个独特的吸收信号,该信号在存在许多不同溶质的情况下,共同报告氢键网络的刚性。本研究全面报道了该组合带在各种化学和生物学相关溶液中如何作为一种内在的集体探针,这些溶液包括不同性质的盐、变性剂、渗透剂、拥挤剂以及形成反胶束和胶束的表面活性剂。虽然我们提到了该组合带的线宽和强度变化,但我们主要关注频率以及频率如何报告液态水的集体氢键网络。我们还评论了经常应用于该谱带的“缔合带”名称,以及如何评估该光谱区域中有时出现在特定种类有机溶质水溶液红外光谱中的离散特征,特别是那些溶质浓度非常高的样品,得出的结论是,这些离散光谱特征大多仅来自溶质,而非关于水的特征。在整个工作中,我们对该组合带的集体和离域报告能力与更多位点特异性振动(如在H₂O中被广泛研究的HDO的OD伸缩振动)的响应进行了对比:该组合带是氢键结构和动力学的独特报告者,与任何局部模式探针有着根本的不同。由于该谱带出现在许多局部模式报告基团的光谱“背景”中,我们注意到在这个光谱区域同时观察局部和集体溶剂动力学的可能性。