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Asymmetry function

Figure 5.5 (A) Time-dependence of the asymmetry function, A(t). (B) Temperature depen-... Figure 5.5 (A) Time-dependence of the asymmetry function, A(t). (B) Temperature depen-...
Fig. 9.1. Physical meaning of the generalised STU parameters and the polarisation function Sp and asymmetry function Sa for scattering of a beam with initial polarisation P, the final polarisation being P. The contraction parameters Tx, Ty and Tz describe the change of initial polarisation along the three axes, while the U parameters describe the rotation in the scattering plane. Fig. 9.1. Physical meaning of the generalised STU parameters and the polarisation function Sp and asymmetry function Sa for scattering of a beam with initial polarisation P, the final polarisation being P. The contraction parameters Tx, Ty and Tz describe the change of initial polarisation along the three axes, while the U parameters describe the rotation in the scattering plane.
Least squares fit of the NAC reference sample synchrotron powder profiles obtained with the Ge(lll) analyzer crystal, (a) NAC (211) Bragg reflection (b) NAC (921) Bragg reflection. The flve other curves are, from left to right, the incident beam source profile, the transfer function of the monochromator, the pure sample profile, the reflection profile of the analyzer, and the axial divergence asymmetry function, respectively. (From Masson, Doryhee, Fitch, by courtesy of J. Appl. Crystallogrfi... [Pg.139]

In order to extract quantitative information from the photoelectron spectra, an asymmetry function is defined as follows... [Pg.78]

Figure 13.22 Approximate time of decay of the d.c. component and the factor of asymmetry as a function of system P.F. during a fault... Figure 13.22 Approximate time of decay of the d.c. component and the factor of asymmetry as a function of system P.F. during a fault...
The functional reaction center contains two quinone molecules. One of these, Qb (Figure 12.15), is loosely bound and can be lost during purification. The reason for the difference in the strength of binding between Qa and Qb is unknown, but as we will see later, it probably reflects a functional asymmetry in the molecule as a whole. Qa is positioned between the Fe atom and one of the pheophytin molecules (Figure 12.15). The polar-head group is outside the membrane, bound to a loop region, whereas the hydrophobic tail is... [Pg.238]

There are other ways in which the lateral organization (and asymmetry) of lipids in biological membranes can be altered. Eor example, cholesterol can intercalate between the phospholipid fatty acid chains, its polar hydroxyl group associated with the polar head groups. In this manner, patches of cholesterol and phospholipids can form in an otherwise homogeneous sea of pure phospholipid. This lateral asymmetry can in turn affect the function of membrane proteins and enzymes. The lateral distribution of lipids in a membrane can also be affected by proteins in the membrane. Certain integral membrane proteins prefer associations with specific lipids. Proteins may select unsaturated lipid chains over saturated chains or may prefer a specific head group over others. [Pg.266]

One area where the concept of atomic charges is deeply rooted is force field methods (Chapter 2). A significant part of the non-bonded interaction between polar molecules is described in terms of electrostatic interactions between fragments having an internal asymmetry in the electron distribution. The fundamental interaction is between the Electrostatic Potential (ESP) generated by one molecule (or fraction of) and the charged particles of another. The electrostatic potential at position r is given as a sum of contributions from the nuclei and the electronic wave function. [Pg.220]

Reductive alkylation with chiral substrates may afford new chiral centers. The reaction has been of interest for the preparation of optically active amino acids where the chirality of the amine function is induced in the prochiral carbonyl moiety 34,35). The degree of induced asymmetry is influenced by substrate, solvent, and temperature 26,27,28,29,48,51,65). Asymmetry also has been obtained by reduction of prochiral imines, using a chiral catalyst 44). Prediction of the major configurational isomer arising from a reductive alkylation can be made usually by the assumption that amine formation comes via an imine, not the hydroxyamino addition compound, and that the catalyst approaches the least hindered side (57). [Pg.91]

The introduction of the p factor yields asymmetry. Finally, the Gompertz function can be used [5] ... [Pg.245]

The simplest and most widely used model to explain the response of organic photovoltaic devices under illumination is a metal-insulaior-metal (MIM) tunnel diode [55] with asymmetrical work-function metal electrodes (see Fig. 15-10). In forward bias, holes from the high work-function metal and electrons from the low work-function metal are injected into the organic semiconductor thin film. Because of the asymmetry of the work-functions for the two different metals, forward bias currents are orders of magnitude larger than reverse bias currents at low voltages. The expansion of the current transport model described above to a carrier generation term was not taken into account until now. [Pg.278]

Thus, the spacing of the chains relative to the neutral, free, swollen size of the buoy blocks is, for a given chemical system and temperature, a unique function of the solvent-enhanced size asymmetry of the diblock polymer and a weak function of the effective Hamaker constant for adsorption. The degree of crowding of the nonadsorbing blocks, measured by a decrease in the left-hand side of Eq. 28, increases with increasing asymmetry of the block copolymer. [Pg.51]

Induction of asymmetry into the /J-lactam-forming process was inefficient with acyclic imines having chiral groups on the nitrogen [19] but efficient with rigid, cyclic chiral imines (Table 3). One of these was used as a chiral template to produce highly functionalized quaternary systems (Eq. 5) [34]. [Pg.163]

The PECD measurement clearly takes the form of a cosine function with an amplitude given entirely in terms of the single chiral parameter, b. It therefore provides exactly the same information content as the y asymmetry factor dehned above [Eq. (8)]. Experimental advantages of examining the PECD rather than the single angular distribution /p(0) are likely to include some cancellation of purely instrumental asymmetries (e.g., varying detection efficiency in the forward-backward directions) and consequent improvements in sensitivity. [Pg.273]

Figure 2. Photoelectron chiral asymmetry factor, y, obtained as a function of electron kinetic energy at hv = 21.2 eV for the (R)- and (S)- enantiomers of glycidol. Also included is a moderate resolution photoelectron spectrum recorded under identical conditions. Data from Refs. [37, 38]. Figure 2. Photoelectron chiral asymmetry factor, y, obtained as a function of electron kinetic energy at hv = 21.2 eV for the (R)- and (S)- enantiomers of glycidol. Also included is a moderate resolution photoelectron spectrum recorded under identical conditions. Data from Refs. [37, 38].

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See also in sourсe #XX -- [ Pg.28 , Pg.359 ]

See also in sourсe #XX -- [ Pg.7 , Pg.78 , Pg.79 , Pg.127 , Pg.128 ]




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