Big Chemical Encyclopedia

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

Articles Figures Tables About

Optical dichroism orientation

In recent years, optical dichroism and birefringence based on photo-induced trans-cis-trans isomerization of azobenzene groups has been observed with preoriented liquid-crystalline polymers [31-35] at temperatures above the glass transition temperature, and also with various amorphous polymers at temperatures well below the glass transition temperature. In the case of a polyimide (see Chart 5.7), a quasi-permanent orientation can be induced [36-38]. Here, the azobenzene groups are rather rigidly attached to the backbone and photoisomerization occurs at room temperature, i.e. 325 °C below the glass transition temperature, Tg = 350°C. This behavior is in accordance with the fact that the isomerization quantum yields of azobenzene compounds are very similar in solution and in polymer matrices 0 trans cis) 0,1 and 0(cis trans) 0.5. [Pg.125]

Dichroism is a property of an optical material that causes light of some wave lengths to be absorbed when the incident light has its electric field vector in a particular orientation and not absorbed when the electric field vector has other orientations. [Pg.231]

Thus, the process of PAN transformation under the effect of IR radiation proceeds with considerable self-acceleration. The irradiation of uniaxially oriented PAN films gives a polymer with a distinct anisotropy of optical properties, dichroism in the visible spectral region in particular. Figure 8 presents dichroism curves [D =/(X)] at various angles (ip) between the polarization plane and the orientation axis. The same figure shows the dependence D =f(uniaxially oriented film. [Pg.16]

Fig. 8. Dichroism of electronic absorption spectra of oriented and nonoriented PAN films after IR irradiation, (a) Dependence of optical density ( >) on the wavelength for various values of (angle between film orientation axis and light polarization plane). Fig. 8. Dichroism of electronic absorption spectra of oriented and nonoriented PAN films after IR irradiation, (a) Dependence of optical density ( >) on the wavelength for various values of <j> (angle between film orientation axis and light polarization plane).
The classical scheme for dichroism measurements implies measuring absorbances (optical densities) for light electric vector parallel and perpendicular to the orientation of director of a planarly oriented nematic or smectic sample. This approach requires high quality polarizers and planarly oriented samples. The alternative technique [50, 53] utilizes a comparison of the absorbance in the isotropic phase (Dj) with that of a homeotropically oriented smectic phase (Dh). In this case, the apparent order parameter for each vibrational oscillator of interest S (related to a certain molecular fragment) may be calculated as S = l-(Dh/Di) (l/f), where / is the thermal correction factor. The angles of orientation of vibrational oscillators (0) with respect to the normal to the smectic layers may be determined according to the equation... [Pg.210]

From measurements of the dichroism of flow of amylose-iodine solutions,161 and from studies of the optical properties of crystalline amylose platelets and iodine-stained platelets,163 it was shown, following the suggestion of Hanes, that a helical configuration of the amylose in this complex is probable. This was later confirmed by x-ray measurements (see p. 378) the iodine atoms were shown to be situated in the core of helically-oriented amylose molecules. [Pg.367]

Optically active chromophores show different absorption for left and right circular polarized light (where the orientation of the polarized light changes periodically). These substances modify a circular polarized beam in such a way that the light is elliptically polarized after leaving the sample, an effect called circular dichroism. [Pg.81]

Using the alternating deposition of the amphiphiles with a carboxyl substituent and arachidic add, noncentrosymmetric LB films (hetero Y-type) were prepared, and molecular orientation and second-order optical nonlinearity in the LB films were evaluated with the linear dichroism [4] and the second-harmonic generation (SHG) measurements, respectively. The SHG measurement procedure is mentioned in the section 1.3. [Pg.301]

Photochemically Triggered Induced Circular Dichroism in Liposomes When an optically inactive chromophore is subject to the effect of optically active environment, optical activity may be induced at the absorption wavelength of the optically inactive chromophore. This phenomenon of induced circular dichroism(ICD) is often observed in polypeptides bearing various achiral chromophores on the side chain( ). The strong chiral environment caused by the peptide helix structure is responsible for this. Distance from, and orientation to, the chiral field decide the degree of ICD appearing on the achiral chromophore. [Pg.216]

This is the form of the scattering matrix for any medium with rotational symmetry even if all the particles are not identical in shape and composition. A collection of optically active spheres is perhaps the simplest example of a particulate medium which is symmetric under all rotations but not under reflection. Mirror asymmetry in a collection of randomly oriented particles can arise either from the shape of the particles (corkscrews, for example) or from optical activity (circular birefringence and circular dichroism). [Pg.413]

Optically, the crystals exhibit a strong dichroism when resting on 6(010), but not "on a(100), the transmitted colours being deep orange for a-axis vibrations and lemon-yellow for the 6- and c-axes. The optic axial plane is c(001), but it has not been possible to determine the several orientations of the two bisectrices. [Pg.96]

If the molecules stand on edge and are oriented by the dipping process, there will exist an optical anisotropy which will manifest itself in dichroism or, if the material is thick enough, in birefringence. On the other hand, if the molecules lie flat, no optical anisotropy will be shown when the material is examined by transmitted light. Thus polarising... [Pg.78]

Several attempts to induce orientation by mechanical treatment have been reviewed 6). Trans-polyacetylene is not easily drawn but the m-rich material can be drawn to a draw ratio of above 3, with an increase in density to about 70% of the close-packed value. More recently Lugli et al. 377) reported a version of Shirakawa polyacetylene which can be drawn to a draw ratio of up to 8. The initial polymer is a m-rich material produced on a Ti-based catalyst of undisclosed composition and having an initial density of 0.9 g cm-3. On stretching, the density rises to 1.1 g cm-3 and optical and ir measurements show very high levels of dichroism. The (110) X-ray diffraction peak showed an azimuthal width of 11°. The unoriented material yields at 50 MPa while the oriented film breaks at a stress of 150 MPa. The oriented material, when iodine-doped, was 10 times as conductive (2000 S cm-1) as the unstretched film. By drawing polyacetylene as polymerized from solution in silicone oil, Basescu et al.15,16) were able to induce very high levels of orientation and a room temperature conductivity, after doping with iodine, of up to 1.5 x 10s S cm-1. [Pg.45]

An example of a relevant optical property is the birefringence of a deformed polymer network.256 This strain-induced birefringence can be used to characterize segmental orientation, and both Gaussian and non-Gaussian elasticity.92,296-302 Infrared dichroism has also been particularly helpful in this regard.82,303 In the case of the crystallizable polysiloxane elastomers, this orientation is of critical importance with regard to strain-induced crystallization, and the tremendous reinforcement it provides.82... [Pg.181]


See other pages where Optical dichroism orientation is mentioned: [Pg.325]    [Pg.421]    [Pg.460]    [Pg.564]    [Pg.25]    [Pg.121]    [Pg.123]    [Pg.373]    [Pg.374]    [Pg.90]    [Pg.540]    [Pg.479]    [Pg.197]    [Pg.541]    [Pg.2966]    [Pg.410]    [Pg.450]    [Pg.80]    [Pg.106]    [Pg.250]    [Pg.433]    [Pg.416]    [Pg.455]    [Pg.461]    [Pg.79]    [Pg.16]    [Pg.413]    [Pg.97]    [Pg.68]    [Pg.293]    [Pg.36]    [Pg.137]    [Pg.74]    [Pg.151]    [Pg.875]   
See also in sourсe #XX -- [ Pg.54 , Pg.57 , Pg.61 , Pg.63 ]




SEARCH



Optical dichroism

Orientation optical

© 2024 chempedia.info