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Reduction of representations

Complex a(s) may be interpreted as representing two mixtures simultaneously, one corresponding to the real, one to the imaginary part. This will not cause any inconsistency with the operations we shall be performing with the ensemble operators. Alternatively, we could simply restrict ourselves to real a(s), as the real numbers suffice for the full reduction of representations of [Pg.48]

Using the reduction of representations of groups given by Eq. (4.46), one then finds that the rotational spectra of linear molecules contain the angular momenta... [Pg.109]

The same rules for the reduction of representations of groups give the following content of angular momentum in each vibrational band of bent molecules... [Pg.109]

In describing the various mechanical properties of polymers in the last chapter, we took the attitude that we could make measurements on any time scale we chose, however long or short, and that such measurements were made in isothermal experiments. Most of the experimental results presented in Chap. 3 are representations of this sort. In that chapter we remarked several times that these figures were actually the result of reductions of data collected at different temperatures. Now let us discuss this technique our perspective, however, will be from the opposite direction taking an isothermal plot apart. [Pg.256]

The reduction of the x representation, like all such reductions, gives a unique set of irreducible representations which is... [Pg.95]

Another source of departure from stoichiometry occurs when cations are reduced, as for example in tire reduction of zinc oxide to yield an oxygen-defective oxide. The zinc atoms which are formed in tlris process dissolve in the lattice, Zn+ ions entering interstitial sites and the coiTesponding number of electrons being released from these dissolved atoms in much the same manner as was found when phosphorus was dissolved in the Group IV semiconductors. The Kroger-Viirk representation of dris reduction is... [Pg.225]

The human-machine interface (usually abbreviated to interface) is a major focus of interest for the HF/E approach to the reduction of human error. A representation of the interface in a CPI context is provided in Figure 2.2. The interface is the boimdary across which information from the process is transduced by sensors and then displayed in a form that can be utilized by the... [Pg.55]

The transformation of the irreducible representations of the molecular point group to those of the site is connected with a reduction of the symme-... [Pg.45]

Figure 3.7 Schematic representation of the reduction of Au (III) ions at the outer layer of the electric double layer in aqueous media [43]. Figure 3.7 Schematic representation of the reduction of Au (III) ions at the outer layer of the electric double layer in aqueous media [43].
Figure 20.6 Schematic representation of the effects of 5-HT reuptake inhibitors on serotonergic neurons, (a) 5-HT is released at the somatodendritic level and by proximal segments of serotonergic axons within the Raphe nuclei and taken up by the 5-HT transporter. In these conditions there is little tonic activation of somatodendritic 5-HTia autoreceptors. At nerve terminals 5-HTib receptors control the 5-HT synthesis and release in a local manner, (b) The blockade of the 5-HT transporter at the level of the Raphe nuclei elevates the concentration of extraneuronal 5-HT to an extent that activates somatodendritic autoreceptors (5-HTia). This leads to neuronal hyperpolarisation, reduction of the discharge rate and reduction of 5-HT release by forebrain terminals, (c) The exposure to an enhanced extracellular 5-HT concentration produced by continuous treatment with SSRIs desensitises Raphe 5-HTia autoreceptors. The reduced 5-HTia function enables serotonergic neurons to recover cell firing and terminal release. Under these conditions, the SSRI-induced blockade of the 5-HT transporter in forebrain nerve terminals results in extracellular 5-HT increases larger than those observed after a single treatment with SSRIs. (Figure and legend taken from Hervas et al. 1999 with permission)... Figure 20.6 Schematic representation of the effects of 5-HT reuptake inhibitors on serotonergic neurons, (a) 5-HT is released at the somatodendritic level and by proximal segments of serotonergic axons within the Raphe nuclei and taken up by the 5-HT transporter. In these conditions there is little tonic activation of somatodendritic 5-HTia autoreceptors. At nerve terminals 5-HTib receptors control the 5-HT synthesis and release in a local manner, (b) The blockade of the 5-HT transporter at the level of the Raphe nuclei elevates the concentration of extraneuronal 5-HT to an extent that activates somatodendritic autoreceptors (5-HTia). This leads to neuronal hyperpolarisation, reduction of the discharge rate and reduction of 5-HT release by forebrain terminals, (c) The exposure to an enhanced extracellular 5-HT concentration produced by continuous treatment with SSRIs desensitises Raphe 5-HTia autoreceptors. The reduced 5-HTia function enables serotonergic neurons to recover cell firing and terminal release. Under these conditions, the SSRI-induced blockade of the 5-HT transporter in forebrain nerve terminals results in extracellular 5-HT increases larger than those observed after a single treatment with SSRIs. (Figure and legend taken from Hervas et al. 1999 with permission)...
Ru 2,2 -bipyridine complexes can form a large number of colored compounds upon successive reduction, with the formal Ru oxidation state from +2 to -4. In the case of highly reduced complexes, proper representation of the electrochromic reaction is actually the reduction of the hgand, not that of the metal center. [Pg.625]

Figure 3.10. Schematic representation of the elementary steps used in microkinetic simulations of the reduction of NO on supported metal particles [23]. The mechanism represented here incorporates adsorption and desorption steps, surface reactions such as NO dimerization and dissociation and N2, N20 and C02 formation, surface oxidation, and mobility of adsorbates. (Figure provided by Professor Libuda and reproduced with permission from Elsevier, Copyright 2005). Figure 3.10. Schematic representation of the elementary steps used in microkinetic simulations of the reduction of NO on supported metal particles [23]. The mechanism represented here incorporates adsorption and desorption steps, surface reactions such as NO dimerization and dissociation and N2, N20 and C02 formation, surface oxidation, and mobility of adsorbates. (Figure provided by Professor Libuda and reproduced with permission from Elsevier, Copyright 2005).
Table 9 The symmetry group and the reduction of the representations of the Cartesian displacements for... Table 9 The symmetry group and the reduction of the representations of the Cartesian displacements for...
The internal coordinates for the water molecule are chosen as changes in the structural parameters defined in Fig. 3. The effect of each symmetry operation of the symmetry group ( 2 on these internal coordinates is specified in Table 2. Clearly, the internal coordinate Ace is totally symmetric, as the characters xy(Aa) correspond to those given for the irreducible representation (IR) Ai. On die other hand, the characters x/(Ar), as shown, can not be identified with a specific IR. By inspection of Table 2, however, it is apparent that the direct sum Ai B2 corresponds to the correct symmetry of these coordinates. In more complicated cases the magic formula can always be employed to achieve the correct reduction of the representation in question. [Pg.331]

Consider the trans isomer of butadiene. Both the symmetry operations that define the group < 2h and the characters of the representation r are given in Table 3. The reduction of this representation leads to Tn =2Bg 2Aa. Thus, two linear combinations of the atomic orbitals can be constructed of symmetry Bg and two others of symmetry A. Their use will factor the secular determinant into two 2x2 blocks, as described in the following paragraph. [Pg.375]

In the enterocyte as it enters the absorptive zone near to the villus tips, dietary iron is absorbed either directly as Fe(II) after reduction in the gastrointestinal tract by reductants like ascorbate, or after reduction of Fe(III) by the apical membrane ferrireductase Dcytb, via the divalent transporter Nramp2 (DCT1). Alternatively, haem is taken up at the apical surface, perhaps via a receptor, and is degraded by haem oxygenase to release Fe(II) into the same intracellular pool. The setting of IRPs (which are assumed to act as iron biosensors) determines the amount of iron that is retained within the enterocyte as ferritin, and that which is transferred to the circulation. This latter process is presumed to involve IREG 1 (ferroportin) and the GPI-linked hephaestin at the basolateral membrane with incorporation of iron into apotransferrin. (b) A representation of iron absorption in HFE-related haemochromatosis. [Pg.250]

Figure 2.86 Schematic representation of variation in the diffusion layer thickness, 6, as a function of time for the reduction of an oxidant O at a fixed planar electrode. [O ] is the concentration of O in the bulk of the solution, [O]0, is the concentration at the electrode surface, x is the distance into the solution from the electrode surface, and du etc, are the diffusion layer thickness at various times etc. Figure 2.86 Schematic representation of variation in the diffusion layer thickness, 6, as a function of time for the reduction of an oxidant O at a fixed planar electrode. [O ] is the concentration of O in the bulk of the solution, [O]0, is the concentration at the electrode surface, x is the distance into the solution from the electrode surface, and du etc, are the diffusion layer thickness at various times etc.

See other pages where Reduction of representations is mentioned: [Pg.110]    [Pg.95]    [Pg.102]    [Pg.81]    [Pg.242]    [Pg.242]    [Pg.243]    [Pg.1826]    [Pg.110]    [Pg.95]    [Pg.102]    [Pg.81]    [Pg.242]    [Pg.242]    [Pg.243]    [Pg.1826]    [Pg.67]    [Pg.69]    [Pg.495]    [Pg.477]    [Pg.588]    [Pg.142]    [Pg.248]    [Pg.295]    [Pg.1]    [Pg.625]    [Pg.194]    [Pg.104]    [Pg.106]    [Pg.165]    [Pg.213]    [Pg.41]    [Pg.11]    [Pg.242]    [Pg.128]   
See also in sourсe #XX -- [ Pg.407 , Pg.408 ]




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