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Coupling, of vectors

Back-ground / Object Edges. A couple of pixels is included in the border between an object and the bottom of the image if one of pixels belongs to the object and the other to the bottom, one can therefore define the border as the totality of pixels of the object that belong to a couple of pixels linked to the main issue. The size of tliis totality corresponds to the number of couples of pixels included in the border and depends on the option of the vector d. [Pg.234]

The matrix of vectors F is thus the defining quantity, and is called the non-adiabatic coupling matrix. It gives the strength (and direction) of the coupling between the nuclear functions associated with the adiabatic electronic states. [Pg.278]

In a similar way the coupling of a third vector to any of the L in Figure 7.4(a) will give the terms arising from three non-equivalent electrons, and so on. [Pg.207]

The coupling between the spin momenta is referred to as xx coupling. The results of coupling of the s vectors can be obtained in a similar way to U coupling with the difference that, since x is always 4, the vector for each electron is always of magnitude 3 ft/2... [Pg.207]

I have elected to include a discussion of the variational principle and perturbational methods, although these are often covered in courses in elementary quantum mechanics. The properties of angular momentum coupling are used at the level of knowing the difference between a singlet and a triplet state. 1 do not believe that it is necessary to understand the details of vector coupling to understand the implications. [Pg.444]

Boys, S. F., Trans. Roy. Soc. [London) A245, 95, Electronic wave functions. VI. Some theorems facilitating the evaluation of Schrodinger integrals of vector-coupled functions. ... [Pg.331]

Hund37 in 1926 and of oxygen and nitric oxide by Van Vleck38 in 1928 were triumphs of the theory of spectra. The magnetic moment of an atom or monatomic ion with Russell-Saunders coupling of the quantum vectors is... [Pg.90]

Figure 5.18 (A) Pulse sequence for homonuclear 2D y-resolved spectroscopy. (B) Effect of 90° H and 180° H pulses on an H doublet. (C) In the absence of coupling, the vectors are refocused by the 180° H pulse after t. This serves to remove any field inhomogeneities or chemical shift differences. Figure 5.18 (A) Pulse sequence for homonuclear 2D y-resolved spectroscopy. (B) Effect of 90° H and 180° H pulses on an H doublet. (C) In the absence of coupling, the vectors are refocused by the 180° H pulse after t. This serves to remove any field inhomogeneities or chemical shift differences.
Table 19.3 Coupling of the spin vectors related to cooperative magnetic effects... Table 19.3 Coupling of the spin vectors related to cooperative magnetic effects...
The rate of a chemical reaction (the chemical flux ), 7ch, in contrast to the above processes, is a scalar quantity and, according to the Curie principle, cannot be coupled with vector fluxes corresponding to transport phenomena, provided that the chemical reaction occurs in an isotropic medium. Otherwise (see Chapter 6, page 450), chemical flux can be treated in the same way as the other fluxes. [Pg.92]

MATLAB supports every imaginable way that one can manipulate vectors and matrices. We only need to know a few of them and we will pick up these necessary ones along the way. For now, we ll do a couple of simple operations. With the vector x and matrix a that we ve defined above, we can perform simple operations such as... [Pg.218]

The wave functions are obtained by vector coupling of the components according to... [Pg.58]

Fig. 4.1. Coupling of the adsorbate low-frequency mode with substrate phonons K level of the adsorbate (a) initial quasicontinuous phonon spectrum of the substrate not perturbed by the adsorbate, bold lines designating the levels which correspond to the specified wave vector K (b) level shifts in the K subsystem caused by the coupling of the adsorbate K mode and substrate phonons (c). Fig. 4.1. Coupling of the adsorbate low-frequency mode with substrate phonons K level of the adsorbate (a) initial quasicontinuous phonon spectrum of the substrate not perturbed by the adsorbate, bold lines designating the levels which correspond to the specified wave vector K (b) level shifts in the K subsystem caused by the coupling of the adsorbate K mode and substrate phonons (c).
The next diagram (FIG. 3) also does not contribute to the partial width for the 0 — W7r° decay. In this case the Lagrangian of the strong coupling of axial-vector mesons to vector and pseudoscalar mesons is derived in a similar way and has the form (Nasriddinov, 1994)... [Pg.293]

Fig. 8.2 Ori entations of an amide NH dipolar coupling bond-vector of the protein ubiquitin. Each cone of orientations is compatible with two different alignment directions adopted by the protein in two different alignment media. The central lines defining each cone correspond to the orientations obtained from the measured dipolar couplings. The outer lines include orientations that are possible if the dipolar coupling values are either increased or decreased by 1 Hz. The angle at which the two cones intersect is defined by ft. The solid dot at the cone intersection determines the orientation of the dipolar coupling vector. (Reproduced with permission from B. E. Ramirez and A. Bax, J. Am. Chem. Soc. 1998, 720, 9106-9107.)... Fig. 8.2 Ori entations of an amide NH dipolar coupling bond-vector of the protein ubiquitin. Each cone of orientations is compatible with two different alignment directions adopted by the protein in two different alignment media. The central lines defining each cone correspond to the orientations obtained from the measured dipolar couplings. The outer lines include orientations that are possible if the dipolar coupling values are either increased or decreased by 1 Hz. The angle at which the two cones intersect is defined by ft. The solid dot at the cone intersection determines the orientation of the dipolar coupling vector. (Reproduced with permission from B. E. Ramirez and A. Bax, J. Am. Chem. Soc. 1998, 720, 9106-9107.)...
Fig. 8.7). On the basis of this similarity they have developed a method to obtain good estimations of Da and R. The use of dipolar couplings of all possible backbone bond-vectors will approximate to an isotropic distribution, provided that they are normalized by taking into account the differences in the gyromagnetic ratio and bond distance. [Pg.189]

Dipolar couplings of side chains can provide valuable structural information. Dipolar couplings for methylene and methyl sites have been applied to protein structure refinement [49]. In a side chain with a C-CH3 moiety, rapid rotation of the methyl group results in an averaged C-H dipolar vector aligned in the direction of the C-C bond. This rapid rotation scales the real value of the C-H dipolar by a factor of —1/3. Therefore, when including methyl dipolar couplings in protein structure refinement, the orientation of the C-CH3 bond is the one that is restricted, rather than the C-H bond. [Pg.191]


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See also in sourсe #XX -- [ Pg.56 , Pg.59 ]




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