Enhanced electric field orientation

Molecular Design for Enhanced Electric Field Orientation of Second-Order Nonlinear Optical... 

Interfacial water molecules play important roles in many physical, chemical and biological processes. A molecular-level understanding of the structural arrangement of water molecules at electrode/electrolyte solution interfaces is one of the most important issues in electrochemistry. The presence of oriented water molecules, induced by interactions between water dipoles and electrode and by the strong electric field within the double layer has been proposed [39-41]. It has also been proposed that water molecules are present at electrode surfaces in the form of clusters [42, 43]. Despite the numerous studies on the structure of water at metal electrode surfaces using various techniques such as surface enhanced Raman spectroscopy [44, 45], surface infrared spectroscopy [46, 47[, surface enhanced infrared spectroscopy [7, 8] and X-ray diffraction [48, 49[, the exact nature of the structure of water at an electrode/solution interface is still not fully understood. 

In the normal-incident transmission measurements of LB films deposited on transparent substrates, the electric vector of the infrared beam is parallel to the film surface (Figure 5A). Therefore, only absorption bands which have the transition moments parallel to the film surface can be detected by this method. On the other hand, in the above-mentioned RA measurements, in which the p-polarized infrared beam is incident upon the LB film prepared on Ag-evaporated substrates at a large angle of incidence, we have a strong electric field perpendicular to the film surface as shown in Figure 5B. Therefore, in this case, only absorption bands which have the transition moments perpendicular to the film surface can be detected with a large intensity enhancement. Thus, if the molecules are highly oriented in the LB films, the peak intensities of particular bands should be different between the transmission and RA spectra. 

Here, Kx and Kz are the X and Z components of the absorption coefficient, and mx and mz are those of the intensity enhancement factor in the RA measurements due to the presence of the Ag film. The second term in the denominator of the right hand side of Eq. (1) was added to take into account the slight contribution of the electric field parallel to the film surface in the RA measurements. After a simple calculation under the condition of the uniaxial orientation, we have... 

In summary, VH F demonstrates the same pattern of solvent dependence as does 2/h h. However, all the subtleties seem to be enhanced. Usually 2/H F decreases in solvents of higher dielectric strength, but an appropriate dipole orientation with respect to the H—C—F group can lead to the opposite result as is observed in vinyl fluoride. This situation is perhaps most likely to occur in mono-fluoro compounds where the fluorine is the principal contributor to the molecular dipole. In either case the electric field effect as postulated with the Pople expression for the contact term produces the correct prediction. 

With capillary electrophoresis (CE), another modern primarily analytically oriented separation methodology has recently found its way into routine and research laboratories of the pharmaceutical industries. As the most beneficial characteristics over HPLC separations the extremely high efficiency leading to enhanced peak capacities and often better detectability of minor impurities, complementary selectivity profiles to HPLC due to a different separation mechanism as well as the capability to perform separations faster than by HPLC are frequently encountered as the most prominent advantages. On the negative side, there have to be mentioned detection sensitivity limitations due to the short path length of on-capillary UV detection, less robust methods, and occasionally problems with run-to-run repeatability. Nevertheless, CE assays have now been adopted by industrial labs as well and this holds in particular for enantiomer separations of chiral pharmaceuticals. While native cyclodextrins and their derivatives, respectively, are commonly employed as chiral additives to the BGEs to create mobility differences for the distinct enantiomers in the electric field, it could be demonstrated that cinchona alkaloids [128-130] and in particular their derivatives are applicable selectors for CE enantiomer separation of chiral acids [19,66,119,131-136]. 

For very small electric fields ( <105 Vm"1), the linear term in E is positive and so the applied electric field enhances the escape of oppositely charged ions from each other. With small electric fields, where only the linear and quadratic terms need be considered, the influence of the electric field on the escape probability is small. Other analytical and numerical techniques have been discussed [327—331], There is little reason to anticipate any correlation of the orientation of an ion-pair when initially formed with the external electric field. Presuming that the distribution of ion-pair orientations is random with respect to the electric field, the escape probability of an ion-pair depends on r0 and E alone [332]. Averaged over 0 < 90 < 27t, eqn. (151) gives... 

Three synthetic approaches to donor-acceptor-substituted conjugated molecules with enhanced orientability in electric fields, potentially applicable to the preparation of electro-optic polymers via electric field poling, are summarized. The three approaches are parallel attachment of chromophores to a common framework, embedding the chromophore in a zwitterion, and head-to-tail oligomerization of chromophores. The oligomerization method as well as the use of dyes as curing agents are briefly discussed in relation to the stability of electric field-induced polar order in polymer matrices. 

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