Park Sungnam, Fayer M D
Department of Chemistry, Stanford University, Stanford, CA 94305, USA.
Proc Natl Acad Sci U S A. 2007 Oct 23;104(43):16731-8. doi: 10.1073/pnas.0707824104. Epub 2007 Oct 11.
Hydrogen bond dynamics of water in NaBr solutions are studied by using ultrafast 2D IR vibrational echo spectroscopy and polarization-selective IR pump-probe experiments. The hydrogen bond structural dynamics are observed by measuring spectral diffusion of the OD stretching mode of dilute HOD in H(2)O in a series of high concentration aqueous NaBr solutions with 2D IR vibrational echo spectroscopy. The time evolution of the 2D IR spectra yields frequency-frequency correlation functions, which permit quantitative comparisons of the influence of NaBr concentration on the hydrogen bond dynamics. The results show that the global rearrangement of the hydrogen bond structure, which is represented by the slowest component of the spectral diffusion, slows, and its time constant increases from 1.7 to 4.8 ps as the NaBr concentration increases from pure water to approximately 6 M NaBr. Orientational relaxation is analyzed with a wobbling-in-a-cone model describing restricted orientational diffusion that is followed by complete orientational randomization described as jump reorientation. The slowest component of the orientational relaxation increases from 2.6 ps (pure water) to 6.7 ps (approximately equal to 6 M NaBr). Vibrational population relaxation of the OD stretch also slows significantly as the NaBr concentration increases.
通过使用超快二维红外振动回波光谱和偏振选择性红外泵浦 - 探测实验,研究了溴化钠溶液中水的氢键动力学。在一系列高浓度溴化钠水溶液中,利用二维红外振动回波光谱测量稀重水(HOD)中OD伸缩模式的光谱扩散,观察氢键结构动力学。二维红外光谱的时间演化产生频率 - 频率相关函数,这允许对溴化钠浓度对氢键动力学的影响进行定量比较。结果表明,以光谱扩散最慢的分量表示的氢键结构的全局重排变慢,并且随着溴化钠浓度从纯水增加到约6M溴化钠,其时间常数从1.7皮秒增加到4.8皮秒。用圆锥内摆动模型分析取向弛豫,该模型描述了受限的取向扩散,随后是描述为跳跃重取向的完全取向随机化。取向弛豫最慢的分量从2.6皮秒(纯水)增加到6.7皮秒(约等于6M溴化钠)。随着溴化钠浓度的增加,OD伸缩振动的振动布居弛豫也显著减慢。