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Polarization depolarization

Light of definite energy and polarization has a selective power to exclusively excite dye molecules whose electronic transition energy and orientation match these parameters. Thus, if a dye is excited by polarized fight, its emission will also be highly polarized. Depolarization occurs only when the time correlation of these selectively excited species is lost due to their rotation or participation in some... [Pg.114]

While it is usually accepted that the solvent polarization/depolarization energy is given in this way to a reasonable accuracy - within the limitations of the Born equation — the question of the mechanism whereby this peculiar state of the solvent may be reached has seldom been considered. The concensus has developed in recent years that this must rely on the random fluctuations of the positions of solvent molecules, sometimes called density fluctuations but there is no analytical formulation of the probability of such extraordinarily localized fluctuations [59]. [Pg.113]

Orientation polarization Depolarization of scattered light (All results negative)... [Pg.44]

The difference of relaxation times in different domains makes it possible to observe the spectrum of one of the domains. Figure 10.23(a), shows the Ti-selected spectrum of PVPh/PEO = 40/60 [34]. Since the Ti of crystalline PEO ( 15 s) is much longer than that of the amorphous phase (—0.1 s), it is possible to observe the spectrum of crystalline PEO selectively (indicated by arrow in Fig. 10.23(a)). On the other hand, for the miscible PVPh-rich blend (PVPh/PEO = 58/42), the crystalline-PEO peak is not appreciable. This is in agreement with the above-mentioned results (Table 10.2). The signals of mobile domains/component polymers can be observed selectively by utilizing the weaker dipolar interaction between H. To name a few examples, the dipolar dephasing [128,131,152], the cross-polarization-depolarization [152] and the pulse saturation transfer [151] techniques have been applied. [Pg.394]

Because lipophilicity is critical and SARs are not, relatively simple explanations of anesthetic activity are still appealing. Thus considering the known fact that such compounds do enter cellular membranes means that they are very likely to become intimately associated with lipoidal components of the membrane matrix that, in addition to the genuine lipids (e.g., myelin membranes in the brain are ca. 80% lipid), will include the larger alkyl and aryl portions of the amino acids of the protein components of the membranes. This may in turn result in a partial closure of the ion channels, thereby inhibiting polarization-depolarization of the membrane. [Pg.567]

Also the system polarizes and depolarizes very slowly. However, the potential is also susceptible to changes in the environment (temperature, humidity), as well as the applied current, so reading must be taken within a reasonable time period while the environment around the structure is reasonably stable. This is particularly important for tidal zones of structures in marine exposure conditions where the polarization/depolarization period should either be through a full tidal cycle or while the steel adjacent to the reference electrode is fully exposed. The full tidal cycle (about 12 h 20 min) is preferred at the steel should be in the same condition at the beginning and the end of the period while its condition will be changing (drying out) during an exposure period... [Pg.179]

Analysis of the obtained RESP charges shows that the charge set generated for the dimer should be used for simulation of longer oligomers. Moreover, the values generated in vacuum would be more adequate for implementation in AMBER, since the additional effects of polarization/depolarization should be accounted for by means of direct interactions with the explicit solvent molecules the charges of which are also based on gas phase calculations... [Pg.478]


See other pages where Polarization depolarization is mentioned: [Pg.123]    [Pg.232]    [Pg.232]    [Pg.651]    [Pg.651]    [Pg.47]    [Pg.80]    [Pg.17]    [Pg.300]    [Pg.300]    [Pg.301]    [Pg.301]    [Pg.580]    [Pg.236]    [Pg.269]    [Pg.360]    [Pg.132]    [Pg.259]    [Pg.156]    [Pg.164]    [Pg.241]   
See also in sourсe #XX -- [ Pg.222 , Pg.348 , Pg.350 ]




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