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Cavity polarity

P-CD. We also observed a significant blue-shift in the 1,8-ANS emission spectrum upon inclusion into the modified CD, from 520 mn as the free probe in aqueous solution to 465 nm in lOmM HP- -CD solution, compared to 492 mn in P-CD. Thus, 1,8-ANS experiences a much lower cavity polarity in HP- -CD than in P-CD. The position of the 1,8-ANS spectral maximum (in v) in various solvents was found to correlate well to the dielectric constant of the solvent the spectral maximum obtained in HP-)5-CD and P-CD corresponded to local... [Pg.45]

There are differences between photons and phonons while the total number of photons in a cavity is infinite, the number of elastic modes m a finite solid is finite and equals 3N if there are N atoms in a three-dimensional solid. Furthennore, an elastic wave has tliree possible polarizations, two transverse and one longimdinal, in contrast to only... [Pg.412]

This shows that the dielectric constant e of a polar solvent is related to the cavity fimction for two ions at large separations. One could extend this concept to define a local dielectric constant z(r) for the interaction between two ions at small separations. [Pg.470]

An alternative approach to obtaining microwave spectroscopy is Fourier transfonn microwave (FTMW) spectroscopy in a molecular beam [10], This may be considered as the microwave analogue of Fourier transfonn NMR spectroscopy. The molecular beam passes into a Fabry-Perot cavity, where it is subjected to a short microwave pulse (of a few milliseconds duration). This creates a macroscopic polarization of the molecules. After the microwave pulse, the time-domain signal due to coherent emission by the polarized molecules is detected and Fourier transfonned to obtain the microwave spectmm. [Pg.2441]

Fig. 6. Free energies of hydration calculated, for a series of polar and non-polar solute molecules by extrapolating using (3) from a 1.6 ns trajectory of a softcore cavity in water plotted against values obtained using Thermodynamic Integration. The solid line indicates an ideal one-to-one correspondence. The broken line is a line of best fit through the calculated points. Fig. 6. Free energies of hydration calculated, for a series of polar and non-polar solute molecules by extrapolating using (3) from a 1.6 ns trajectory of a softcore cavity in water plotted against values obtained using Thermodynamic Integration. The solid line indicates an ideal one-to-one correspondence. The broken line is a line of best fit through the calculated points.
The PCM algorithm is as follows. First, the cavity siuface is determined from the van der Waals radii of the atoms. That fraction of each atom s van der Waals sphere which contributes to the cavity is then divided into a nmnber of small surface elements of calculable surface area. The simplest way to to this is to define a local polar coordinate frame at tlie centre of each atom s van der Waals sphere and to use fixed increments of AO and A(p to give rectangular surface elements (Figure 11.22). The surface can also be divided using tessellation methods [Paschual-Ahuir d al. 1987]. An initial value of the point charge for each surface element is then calculated from the electric field gradient due to the solute alone ... [Pg.612]

The most popular of the SCRF methods is the polarized continuum method (PCM) developed by Tomasi and coworkers. This technique uses a numerical integration over the solute charge density. There are several variations, each of which uses a nonspherical cavity. The generally good results and ability to describe the arbitrary solute make this a widely used method. Flowever, it is sensitive to the choice of a basis set. Some software implementations of this method may fail for more complex molecules. [Pg.212]

Grown Macroring Inclusion Compounds (Coronates). Prototypical crown macrorings are cycHc ohgoethers such as given by formulae (1—4) (Fig. 3). Inside the hng they make available a negatively polarized cavity capable of accommodating metal ions to form crown cation inclusion... [Pg.61]

Molecular Interactions. Various polysaccharides readily associate with other substances, including bile acids and cholesterol, proteins, small organic molecules, inorganic salts, and ions. Anionic polysaccharides form salts and chelate complexes with cations some neutral polysaccharides form complexes with inorganic salts and some interactions are stmcture specific. Starch amylose and the linear branches of amylopectin form inclusion complexes with several classes of polar molecules, including fatty acids, glycerides, alcohols, esters, ketones, and iodine/iodide. The absorbed molecule occupies the cavity of the amylose helix, which has the capacity to expand somewhat to accommodate larger molecules. The starch—Hpid complex is important in food systems. Whether similar inclusion complexes can form with any of the dietary fiber components is not known. [Pg.71]

Figures 17A and 17B (p. 183) show energy as a function of rotation for a series of 1-substituted acetaldehydes, with 6 = 0° in the syn conformation and 6 = 180° in the anti conformation. The calculations were done using the PM3 method. Figure 17A for a vacuum, whereas Fig. 17B is for a solvent cavity with a dielectric constant of 4." The table gives the calculated barriers. Discuss the following aspects (a) rationalize the order Br > Cl > F for syn conformers (b) rationalize the shift to favor the am. conformation in the more polar environment. [Pg.182]


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See also in sourсe #XX -- [ Pg.32 , Pg.33 , Pg.42 , Pg.43 , Pg.46 , Pg.47 , Pg.48 , Pg.50 ]




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Polarized solvent cavity

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