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Vibrational mode stretching

Structure No. of oxygen atoms No. of vibrational modes Stretchings Frequency region (cm- ) Deformations ... [Pg.112]

The transfer of energy back and forth between vibrational modes (stretches, bends, wags, etc.) and torsional modes implies that a torsion is a vibration, and we have already defined it as such. Moreover, because the other vibrations are quantized, it makes sense that torsional modes are quantized also, as we describe in the next Going Deeper highlight. The... [Pg.94]

Variational RRKM theory is particularly important for imimolecular dissociation reactions, in which vibrational modes of the reactant molecule become translations and rotations in the products [22]. For CH —> CHg+H dissociation there are tlnee vibrational modes of this type, i.e. the C—H stretch which is the reaction coordinate and the two degenerate H—CH bends, which first transfomi from high-frequency to low-frequency vibrations and then hindered rotors as the H—C bond ruptures. These latter two degrees of freedom are called transitional modes [24,25]. C2Hg 2CH3 dissociation has five transitional modes, i.e. two pairs of degenerate CH rocking/rotational motions and the CH torsion. [Pg.1016]

Figure Bl.22.6. Raman spectra in the C-H stretching region from 2-butanol (left frame) and 2-butanethiol (right), each either as bulk liquid (top traces) or adsorbed on a rough silver electrode surface (bottom). An analysis of the relative intensities of the different vibrational modes led to tire proposed adsorption structures depicted in the corresponding panels [53], This example illustrates the usefiilness of Raman spectroscopy for the detennination of adsorption geometries, but also points to its main limitation, namely the need to use rough silver surfaces to achieve adequate signal-to-noise levels. Figure Bl.22.6. Raman spectra in the C-H stretching region from 2-butanol (left frame) and 2-butanethiol (right), each either as bulk liquid (top traces) or adsorbed on a rough silver electrode surface (bottom). An analysis of the relative intensities of the different vibrational modes led to tire proposed adsorption structures depicted in the corresponding panels [53], This example illustrates the usefiilness of Raman spectroscopy for the detennination of adsorption geometries, but also points to its main limitation, namely the need to use rough silver surfaces to achieve adequate signal-to-noise levels.
Figure Bl.25.12 illustrates the two scattering modes for a hypothetical adsorption system consisting of an atom on a metal [3]. The stretch vibration of the atom perpendicular to the surface is accompanied by a change m dipole moment the bending mode parallel to the surface is not. As explained above, the EELS spectrum of electrons scattered in the specular direction detects only the dipole-active vibration. The more isotropically scattered electrons, however, undergo impact scattering and excite both vibrational modes. Note that the comparison of EELS spectra recorded in specular and off-specular direction yields infomiation about the orientation of an adsorbed molecule. Figure Bl.25.12 illustrates the two scattering modes for a hypothetical adsorption system consisting of an atom on a metal [3]. The stretch vibration of the atom perpendicular to the surface is accompanied by a change m dipole moment the bending mode parallel to the surface is not. As explained above, the EELS spectrum of electrons scattered in the specular direction detects only the dipole-active vibration. The more isotropically scattered electrons, however, undergo impact scattering and excite both vibrational modes. Note that the comparison of EELS spectra recorded in specular and off-specular direction yields infomiation about the orientation of an adsorbed molecule.
Figure 7-13. Cross-terms combining internal vibrational modes such as bond stretch, angle bend, and bond torsion within a molecule. Figure 7-13. Cross-terms combining internal vibrational modes such as bond stretch, angle bend, and bond torsion within a molecule.
Normal modes of vibration, with their corresponding normal coordinates, are very satisfactory in describing the low-lying vibrational levels, usually those with u = 1 or 2, which can be investigated by traditional infrared absorption or Raman spectroscopy. For certain types of vibration, particularly stretching vibrations involving more than one symmetrically equivalent terminal atom, this description becomes less satisfactory as v increases. [Pg.187]

The comparison of the vibrational modes energies, determined by i) Raman scattering, ii) fluorescence, iii) ab initio calculation, and iv) absorption, is reported in Table 6-5. We note that, as in the case of T4 [64], the C=C stretching mode of 1460 cm-1 in the ground slate decreases its frequency significantly (1275 cm-1) in the first excited electronic state. [Pg.416]

Because an applied field in the y direction Ev can induce a dipole M with a component in the x direction Mx as well as the component in the y direction My, it is necessary that we specify the components of the polarizability tensor by two subscripts (Fig. 3). If the bond A—B of a diatomic molecule stretches during a vibrational mode, Mx and Mv will vary and therefore the corresponding polarizability tensor components will vary. [Pg.299]

FIGURE 2 la The three normal vibrational modes of 11,0. Two of these modes are principally stretching motions of the bonds, but mode v2 is primarily bending, (b) The four normal vibrational modes of C02. The first two are symmetrical and antisymmetrical stretching motions, and the last two are perpendicular bending motions. [Pg.217]

Microscopy methods based on nonlinear optical phenomena that provide chemical information are a recent development. Infrared snm-frequency microscopy has been demonstrated for LB films of arachidic acid, allowing for surface-specific imaging of the lateral distribution of a selected vibrational mode, the asymmetric methyl stretch [60]. The method is sensitive to the snrface distribntion of the functional gronp as well as to lateral variations in the gronp environmental and conformation. Second-harmonic generation (SHG) microscopy has also been demonstrated for both spread monolayers and LB films of dye molecules [61,62]. The method images the molecular density and orientation field with optical resolution, and local qnantitative information can be extracted. [Pg.67]

The Raman spectra of WO3, 25-NiO-TiO2/30-WO3, 25-Ni0-Ti02/15-W03, 25- NiO-Ti02/5-W03, and Ti02 under ambient conditions are presented in Fig. 1. The WO3 structure is made up distorted WO3 octahedra. The major vibrational modes of WO3 are located at 808, 714, and 276 cm, and have been assigned to the W=0 stretching mode, the W=0 bending mode, and the W-O-W deformation mode, respectively [7]. The Raman spectrum of the 25-... [Pg.269]

Fig.2 shows the infrared absorption spectrum of the tin oxide film. In order to analyze the molecular structure of the deposited film, we deposited the tin oxide film on a KBr disc with thickness of 1 mm and diameter of 13 mm. Various peaks formed by surface reaction are observed including O-H stretching mode at 3400 cm, C=C stretching mode at 1648 cm, and Sn02 vibration mode at 530 cm. The formation of sp structure with graphite-like is due to ion bombardment with hydrogen ions at the surface and plasma polymerization of methyl group with sp -CHa. [Pg.386]

It is important from a practical viewpoint to predict the shear viscosity of mixtures from those of pure melts. For alkali nitrate melts, a linear dependence has been found between the reorientational line width obtained by Raman measurements and the ratio of temperature divided by shear viscosity.For NO3 ions, the depolarized Raman scattering from 1050cm" total stretching vibrational mode (Al) has a contribution to the line width L, which is caused by the reorientational relaxation time of the Csv axis of this ion. The Stokes-Einstein-Debye(SED) relation establishes a relation between the shear viscosity r of a melt and the relaxation time for the reorientation of a particle immersed in it ... [Pg.177]


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See also in sourсe #XX -- [ Pg.9 , Pg.24 , Pg.26 ]




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