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Current directionality

Figure 4.1 Detection by degenerate superposed absorber states, (a) Scheme of levels relevant to the pumping of the +) state and its photoionization by orthogonally polarized LO and SL fields, (b) Geometry of illumination, DC Stark mixing, and current directionality. The sample is divided by a potential barrier (dark rim) into two regions where separate currents arise for cross-correlation measurements, (c) The odd symmetry part (with respect to of the photoelectronic momentum distribution, which is responsible for Jy. and is associated widi die cross product of the fields. Figure 4.1 Detection by degenerate superposed absorber states, (a) Scheme of levels relevant to the pumping of the +) state and its photoionization by orthogonally polarized LO and SL fields, (b) Geometry of illumination, DC Stark mixing, and current directionality. The sample is divided by a potential barrier (dark rim) into two regions where separate currents arise for cross-correlation measurements, (c) The odd symmetry part (with respect to of the photoelectronic momentum distribution, which is responsible for Jy. and is associated widi die cross product of the fields.
Contrary to systems possessing an inversion center in which the interference between a one-photon and a two-photon process can only lead to phase control of differential properties, e.g., current directionality [29,54,95,96], we have shown that the CPT process of broken symmetry systems allows us to control integral properties as well, a prime example of which is the control of the excited states population of two enantiomers. [Pg.87]

Figure 16.1 Typical ventricular action potential. Corresponding ion channels and electric currents at phases 0-4 are labeled. The contributions and directionality (influx vs efflux) of each ion current at corresponding time points are indicated at the bottom. APD60 and APD90 is the action potential duration at 60% and 90% of repolarization respectively. (Reprinted from [19], with permission from Elsevier). Figure 16.1 Typical ventricular action potential. Corresponding ion channels and electric currents at phases 0-4 are labeled. The contributions and directionality (influx vs efflux) of each ion current at corresponding time points are indicated at the bottom. APD60 and APD90 is the action potential duration at 60% and 90% of repolarization respectively. (Reprinted from [19], with permission from Elsevier).
It is our current opinion that all etching anisotropy or directionality is caused by energetic particle bombardment (primarily ions but in some cases, electrons). Other factors such as the degree of fluorine deficiency in the discharge can influence the... [Pg.21]

Two points should be added to these conclusions. First, if the role of H-bonds appears so fundamental in biophysics and biochemistry that H-bonds may be declared the bonds of life , mainly thanks to the presence of H2O molecules in aU biomedia and to the fundamental role they play there, their action is not limited to these media. The HjO molecule being ubiquitous, thanks to its exceptional possibilities to establish H-bonds, H-bonds are also often encountered in chemistry, where such terms as H-bonded solvents, hydrophilic or hydrophobic groups or molecules are currently encountered and well taken into account, even if a more precise understanding of the role that these HjO molecules play is often needed. They are, also often encountered in physics where H2O molecules are also currently met. Physicists, however, are less aware of their fundamental role. We have seen that the dynamics of HjO molecules in liquid water is yet not understood at all. It is studied by recent time-resolved nonlinear IR methods that are stiU the domain of physicists and also by theoretical methods of molecular dynamics (MD) that have up to now not succeeded in incorporating the directionality of H-bonds in the huge H-bond network of liquid water and consequently the fundamental role rapid rotations (librations) of these very small H2O molecules play. In another... [Pg.309]

The synthesis of alternating copolymers from carbon monoxide (CO) and olefins using palladium catalysts is currently an area of intense research. In cases where a-olefins are used, the regiochemistry (head/tail orientations) and stereochemistry (tacticity) of olefin insertion have a strong influence on the physical and mechanical properties of the polymers. Unlike regioregular a-olefins homopolymers, these copolymers have a directionality along the polymer backbone due to the incorporation of CO. Therefore isotactic, regioregular CO/a-olefin polymers are chiral by virtue of their main-chain stereochemistry (Scheme 11). [Pg.1265]

The last paragraph of a chapter like this one asks the writer to predict if the non-covalent interaction of anions with jt-system will be as important and useful as the nowadays well-established cation-n interaction. We are cautious in answering this question affirmatively, but we have to confess that we are currently working in the construction of synthetic receptors for anions that do incorporate electron deficient ir-aromatic systems. We hope that our designs will be valuable for the experimental evaluation of the anion-JT interaction in solution and we will report shortly our findings. Once the strength of the anion-jt interaction in solution is determined, it will be easier to evaluate its possible use in the construction of selective receptors for anions making use of the directionality properties that we have discussed in the chapter. [Pg.172]

Much of our current knowledge of intermolecular interactions has been derived from the study of crystal structures. For example, it was not until an extensive survey of 1509 N—H---0=C hydrogen bonds in CSD structures that the O lone pair directionality of this key interaction was first recognized [31]. Another example is the detailed study of hydrogen bond geometries in 15 globular proteins carried out by Baker and Hubbard [32] and these hydrogen bond definitions, derived nearly 30 years... [Pg.86]

Directionalization of the azimuth pattern is realized by proper distribution of the feed currents to individual panels in the same layer. Stacking layers provides gains comparable with top-mounted antennas. [Pg.1551]


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See also in sourсe #XX -- [ Pg.87 ]




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