Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Static interaction

In order to account for the optical absorption and emission bands of the ABe center, we must first determine its energy levels A, by solving the Schrodinger equation  [Pg.152]


V..(R) is the static interaction for elastic scattering. The Bom scattering amplitude is a pure fiinction only of... [Pg.2020]

The local wavenumber of relative motion under the static interaction is given by... [Pg.2043]

Micelles are aggregates of surfactants and are capable of solubilizing large quantities of hydrophobic substances ionic reagents are also taken up due to electro-static interactions. [Pg.148]

Other corrections, besides those for static interactions, are important for certain quenchers. For example, acrylamide quenching is often used to help determine the relative solvent accessibility of aromatic residue side chains. In addition to a correction for static quenching,(60,66) acrylamide quenching data for tyrosine residues require both primary and secondary inner filter corrections since acrylamide absorbs both 280- and 305-nm light.(67)... [Pg.19]

RNA. Both proteins contain no tryptophan S8 contains three tyrosines, and S15 contains two tyrosines. The tyrosine emission of these two proteins represents a case in which the quantum yield is higher in the native than the denatured protein. The average fluorescence lifetime, however, was little affected by denaturation no change was observed for S8, and the average lifetime decreased about 12% for S15. The collisional quenchers 1 and Cs + had essentially equivalent access to the tyrosines of both proteins, either in the native or denatured state, and comparison of the bimolecular quenching constants with that of free tyrosine suggested that the tyrosines were all well exposed. The mechanism for the reduction in quantum yield upon denaturation, apparently a static interaction, has not been elucidated. [Pg.27]

P. B. Contino and W. R. Laws, Rotamer-specific fluorescence quenching in tyrosinamide Dynamic and static interactions, J. Fluorescence 1, 5-13 (1991). [Pg.55]

Once synthesized several factors influence the particular leaflet of the membrane lipid bilayer where the lipids reside. One is static interactions with intrinsic and extrinsic membrane proteins which, by virtue of their mechanism of biosynthesis, are also asymmetric with respect to the membrane. The interaction of the cytoplasmic protein, spectrin with the erythrocye membrane has been the subject of a number of studies. Coupling of spectrin to the transmembrane proteins, band 3 and glycophorin 3 via ankyrin and protein 4.1, respectively, has been well documented (van Doit et al, 1998). Interaction of spectrin with membrane lipids is still somewhat conjectural but recent studies have characterized such interactions more precisely. O Toole et al. (2000) have used a fluorescine derivative of phosphatidylethanolamine to investigate the binding affinity of specttin to lipid bilayers comprised of phosphatidylcholine or a binary mixture of phosphatidylcholine and phosphatidylserine. They concluded on the basis... [Pg.45]

Effect of pH The pH of a solution affects the solubilization characteristics of a protein primarily in the way in which it modifies the charge distribution over the protein surface. At pH values below its isoelectric point (pi), or point of zero net charge, a protein acquires a net positive charge, while above its pi the protein will be negatively charged. Thus, if eleetro-static interactions are the dominant factor, solubilization should be possible only with anionic surfactants at pH values less than the pi of the protein because at values above pi, eleetrostatic repulsion would inhibit solubilization. The opposite effeet would be anticipated in the case of cationie surfactants. [Pg.664]

Using reflectometry, Barten etal. [259] have investigated adsorption of quater-nized poly-2-vinyl pyridine, of a fixed charge per monomer, on a gold electrode. The total adsorbed amount of the compound decreased linearly with the double-layer potential of gold. Adsorption proceeded up to a relatively high doublelayer potential and was accompanied by a relatively high contribution of nonelectro-static interactions. [Pg.870]

The initial building-up of the carbon magnetization via polarization transfer is characterized with the spin-lock cross-polarization time Tcir It is sensitive to the static interactions, i.e. transfer of the polarization via static dipolar interactions (proportional to e J). Hence, the shortest TCH will have carbons a) in more rigid systems and b) with more directly attached protons, particularly the CH2 (or... [Pg.78]

Prior adsorption of water and alcohols onto the dehydrated surface can drastically change the interaction of that surface with the adsorbed species of interest. These additives generally render the surface more homogeneous and can be used to Influence dynamic behavior and static interactions. [Pg.3]

The temperature dependence of AH2 for chloral-PC (Fig. 37) shows that the motions of phenyl rings occur above -80°C. Furthermore, the doublet shape observed for the lH spectrum above room temperature presents a splitting constant of 25 d= 0.2 G, which corresponds to the static interaction between the 2,3 phenyl protons, indicating that the phenyl motions do not affect the dipole-dipole interaction parallel to the 1,4 phenyl axis. A quantitative analysis of the intra- and inter molecular contributions to AH2 leads to the conclusion that the phenyl motions correspond to either isolated or concerted rotations around the 1,4 axis, with little (if any) reorientation of this axis. In addition, it excludes other motions as crankshaft motions, or motion of the phenyl-ethylenic unit as a group. The decrease of AH2 above - 40 °C could be intermolecular in nature. [Pg.73]

The results do display a parallelism in reaction for the two pyrimidine polynucleotides. This parallelism is to that described earlier in static interactions of arginine-rich and lysine-rich proteinoids with polynucleotides 57). This parallelism suggests for the dipeptides a synthetic mechanism in which one kind of amino acid is bound by the polynucleotide while the other amino acid is reacted with the bound one. [Pg.75]

Fig. 9.39 Structural representation of the exTTF C60 1 1 pincer-like complexes, demonstrating the effect of re-re-static interactions between the two aromatic systems... Fig. 9.39 Structural representation of the exTTF C60 1 1 pincer-like complexes, demonstrating the effect of re-re-static interactions between the two aromatic systems...
Figure 15.1a shows a typical 2H NMR spectrum obtained in a deuterated PDMS network at room temperature, in the absence of an external constraint [23]. The half-height linewidth is very small (about 60 Hz) compared to the static interaction Vq. This means... [Pg.561]

Here Lw is the contour length of the chain. In an effort to generalize Eq. (14) for non-theta solutions, Reed et al. [46] have provided an ad hoc treatment by combining theories of Odijk [35], Odijk and Houwaart [36], Skolnick and Fixman [37], and Gupta and Forsman [49]. Here they append an additional contribution f30 to A arising from short-ranged non-electro-static interactions, so that f3 of Eq. (11) is given by... [Pg.35]

The /i+ moderation processes involve dominantly electro static interaction and there is no muon depolarization in strong axial magnetic fields (B 0.16 T) [10]. At low fields the tof = 0 atomic states are populated to 50 % which means a corresponding reduction of the polarization due to the muon spin oscillation at the hyperfine frequency Avhfs-... [Pg.84]


See other pages where Static interaction is mentioned: [Pg.2028]    [Pg.2045]    [Pg.800]    [Pg.801]    [Pg.801]    [Pg.610]    [Pg.181]    [Pg.390]    [Pg.152]    [Pg.153]    [Pg.155]    [Pg.157]    [Pg.159]    [Pg.278]    [Pg.707]    [Pg.83]    [Pg.490]    [Pg.153]    [Pg.110]    [Pg.8]    [Pg.35]    [Pg.35]    [Pg.39]    [Pg.67]    [Pg.171]    [Pg.216]    [Pg.243]    [Pg.246]    [Pg.178]    [Pg.29]    [Pg.329]   
See also in sourсe #XX -- [ Pg.35 , Pg.39 , Pg.67 , Pg.97 , Pg.98 , Pg.110 , Pg.128 , Pg.129 , Pg.243 ]




SEARCH



Electron-phonon interaction static effects

Interaction with static magnetic fields

Molecular statics interactions

© 2024 chempedia.info