Liquid linear spectroscopic studies

Other Linear Spectroscopic Studies at the Neat Liquid/Liquid Interface... 

Another approach used in the empirical characterization of liquid polarity is the study of the outcome of a chemical reaction. Earle et al. [216] report a preliminary study of the keto-enol tautomerization of pentane-2,4-dione, and create an empirical correlation between the degree of tautomerization and the dielectric constant of molecular liquids. They then predict dielectric constants for a series of ILs based on the observed keto-enol equilibrium the values range from 40 to 50, slightly higher than those of short-chain alcohols. A more detailed study by Angelini et al. [217] considers the tautomerization of a nitroketone complex in a series of five imidazolium-based ILs. The results, parameterized as a linear free energy analysis of the behavior of the equilibrium constant, indicates an overall polarity comparable to that of acetonitrile, consistent with the partitioning and spectroscopic studies referenced above. 

Spectroscopic studies of liquid interfaces provide important information about the composition and structure of the interfacial region. Early work was mainly carried out at the solid liquid interface and involved techniques such as neutron and X-ray diffraction, and reflection FTIR spectroscopy. More recently, powerful techniques have been developed to study the liquid liquid and liquid gas interfaces. These studies are especially important because of their relevance to biological systems such as cell membranes. The techniques described here are second-harmonic generation (SHG) and vibrational sum frequency spectroscopy (VSFS). They are both second-order non-linear optical techniques which are specific to the interfacial region. Since the second-order effects involve signals of low intensity, they rely on high-power lasers. 

Bauman D, Killet C, Boiadjiev SE, Lightner DA, Schonhofer A and Kuball H-G (1996) Linear and circular dichroism spectroscopic study of P, P -dimethylmesobilirubin-XIIIa oriented in a nematic liquid crystal. Journal of Physical Chemistry 100 11546-11558. 

A key requirement for in-situ spectroscopic methods in these systems is surface specificity. At Uquid/Uquid junctions, separating interfacial signals from the overwhelmingly large bulk responses in linear spectroscopy is not a trivial issue. On the other hand, non-Unear spectroscopy is a powerful tool for investigating the properties of adsorbed species, but the success of this approach is closely linked to the choice of appropriate probe molecules (besides the remarkably sensitivity of sum frequency generation on vibrational modes of water at interfaces). This chapter presents an overview of linear and non-linear optical methods recently employed in the study of electrified liquid/liquid interfaces. Most of the discussion will be concentrated on the junctions between two bulk liquids under potentio-static control, although many of these approaches are commonly employed to study liquid/air, phospholipid bilayers, and molecular soft interfaces. 

In liquids and dense gases where collisions, intramolecular molecular motions and energy relaxation occur on the picosecond timescales, spectroscopic lineshape studies in the frequency domain were for a long time the principle source of dynamical information on the equilibrium state of manybody systems. These interpretations were based on the scattering of incident radiation as a consequence of molecular motion such as vibration, rotation and translation. Spectroscopic lineshape analyses were intepreted through arguments based on the fluctuation-dissipation theorem and linear response theory (9,10). In generating details of the dynamics of molecules, this approach relies on FT techniques, but the statistical physics depends on the fact that the radiation probe is only weakly coupled to the system. If the pertubation does not disturb the system from its equilibrium properties, then linear response theory allows one to evaluate the response in terms of the time correlation functions (TCF) of the equilibrium state. Since each spectroscopic technique probes the expectation value... 

PM3-PIF was implemented in DivCon, a semiempirical linear scaling code and then coupled with Tinker [69], a molecular dynamics code. With the DivCon/Tinker set of programs we calculated molecular dynamics trajectories for a system formed with 210 water molecules and one Br2 molecule for a total of 150 ps. Several interesting questions about bromine in liquid water solution might be addressed with this study. For example Is the hydration of a non polar but polarizable solute, hydrophobic or hydrophilic , To what extent the spectroscopic behavior of bromine in liquid water is the result of the closest neighbors interactions In this work we will address the latter since it pertains to the discussion about the performance of different methods to evaluate the transition energies to the excited states and we will leave a more detailed description of bromine hydration to a forthcoming report. 

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