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Secondary localization

The electrons modify the magnetic field experienced by the nucleus. Chemical shift is caused by simultaneous interactions of a nucleus with surrounding electrons and of the electrons with the static magnetic field B0. The latter induces, via electronic polarization and circulation, a secondary local magnetic field which opposes B0 and therefore shields the nucleus under observation. Considering the nature of distribution of electrons in molecules, particularly in double bonds, it is apparent that this shielding will be spatially anisotropic. This effect is known as chemical shift anisotropy. The chemical shift interaction is described by the Hamiltonian... [Pg.204]

Biochemically there are four major classifications of protein structure primary (amino acid sequence), secondary (local spatial arrangement), tertiary (overall 3D structure) and quaternary (protein complex stmcture). (Figure 1.8)... [Pg.17]

Numerous isoline diagrams revealed that the optimum experimental conditions are low temperature (<20°C), 10-14% catalyst, and high pressure (>25 bar). There is also a secondary local maximum at low pressure (1 bar) and higher temperature (80 °C). Simultaneous optimization by model-space analysis gave the eperi-mental settings 80°C, 1 bar H2 partial pressure, 11.4 % catalyst. [Pg.382]

Fig. 1.10 Left structural diagram of butane. Center coarse-grained model of butane using CH3 and CH2 groups. Right torsion (or dihedral) potential energy showing locations of local minimum corresponding to trans (global minimum) and gauche (secondary local minimum) states... Fig. 1.10 Left structural diagram of butane. Center coarse-grained model of butane using CH3 and CH2 groups. Right torsion (or dihedral) potential energy showing locations of local minimum corresponding to trans (global minimum) and gauche (secondary local minimum) states...
Another DMA analysis is shown in Fig. 4.170 for poly(vinyl chloride), [-CHCl-CHjlx- The data for G, G", and tan 6 are given as a function of temperature for one frequency. The glass transition occurs at about 300 K, as indicated by the drop in G and the peaks in G" and tan 6. In addition, there is a broad peak in G" and in tan 6, indicating a secondary, local relaxation in the glassy state. Semicrystalline... [Pg.423]

FIGURE 7 The secondary (local) minimum structure of the dimethyinitramine complex with methyl alcohol. The carbon atoms are gray, hydrogens—white, nitrogens—blue, and oxygen—red. (From Bukowski etal., 1999.)... [Pg.158]

An example of calculation of a shock tube flow with combustion and detonation were presented in Ref. 5. It was found that "/i>-layer aflfects dramatically transition to detonation of the Chapman-Jouguet type. This transition occurs after formation of the p-layer, and secondary local explosion in the re on of p-layer takes place. The space-time pressure diagrams and variation of the detonation wave velocity in time are presented schematically in Fig. 2. [Pg.289]

The secondary winding of such transformers is rather vulnerable if it is exposed to humid climate. They often develop short circuits within the secondary. Local repair is possible if proper interlayer insulation could be secured combined with vacuum Impregna t ion. [Pg.254]

Characterization and influence of electrohydro dynamic secondary flows on convective flows of polar gases is lacking for most simple as well as complex flow geometries. Such investigations should lead to an understanding of flow control, manipulation of separating, and accurate computation of local heat-transfer coefficients in confined, complex geometries. The typical Reynolds number of the bulk flow does not exceed 5000. [Pg.496]

The autoclave is not the only component of an LDPE plant which may be exposed to a decomposition. Local hot spots in a secondary compressor may initiate a decomposition reaction consequendy it is necessary to protect these units from serious overpressure by pressure relieving devices and to release the products of the decomposition reactions safely. The problem of the aerial decomposition referred to eadier has been largely overcome by rapidly quenching the decomposition products as they enter the vent stack. [Pg.98]

The distribution of current (local rate of reaction) on an electrode surface is important in many appHcations. When surface overpotentials can also be neglected, the resulting current distribution is called primary. Primary current distributions depend on geometry only and are often highly nonuniform. If electrode kinetics is also considered, Laplace s equation stiU appHes but is subject to different boundary conditions. The resulting current distribution is called a secondary current distribution. Here, for linear kinetics the current distribution is characterized by the Wagner number, Wa, a dimensionless ratio of kinetic to ohmic resistance. [Pg.66]

That this is not always the case should be expected. In fact, if it was not for heterogeneous localization of some flow phenomena, it would be very diflicult to initiate secondary explosives, or to effect shock-induced chemical reactions in solids. Heterogeneous shear deformation in metals has also been invoked as an explanation for a reduction in shear strength in shock compression as compared to quasi-isentropic loading. We present here a brief discussion of some aspects of heterogeneous deformation in shock-loaded solids. [Pg.241]

Figure 1.1 The amino acid sequence of a protein s polypeptide chain is called Its primary structure. Different regions of the sequence form local regular secondary structures, such as alpha (a) helices or beta (P) strands. The tertiary structure is formed by packing such structural elements into one or several compact globular units called domains. The final protein may contain several polypeptide chains arranged in a quaternary structure. By formation of such tertiary and quaternary structure amino acids far apart In the sequence are brought close together in three dimensions to form a functional region, an active site. Figure 1.1 The amino acid sequence of a protein s polypeptide chain is called Its primary structure. Different regions of the sequence form local regular secondary structures, such as alpha (a) helices or beta (P) strands. The tertiary structure is formed by packing such structural elements into one or several compact globular units called domains. The final protein may contain several polypeptide chains arranged in a quaternary structure. By formation of such tertiary and quaternary structure amino acids far apart In the sequence are brought close together in three dimensions to form a functional region, an active site.
Secondary structure occurs mainly as a helices and p strands. The formation of secondary structure in a local region of the polypeptide chain is to some extent determined by the primary structure. Certain amino acid sequences favor either a helices or p strands others favor formation of loop regions. Secondary structure elements usually arrange themselves in simple motifs, as described earlier. Motifs are formed by packing side chains from adjacent a helices or p strands close to each other. [Pg.29]


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