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Crystals, electric field molecular

As witli tlie nematic phase, a chiral version of tlie smectic C phase has been observed and is denoted SniC. In tliis phase, tlie director rotates around tlie cone generated by tlie tilt angle [9,32]. This phase is helielectric, i.e. tlie spontaneous polarization induced by dipolar ordering (transverse to tlie molecular long axis) rotates around a helix. However, if tlie helix is unwound by external forces such as surface interactions, or electric fields or by compensating tlie pitch in a mixture, so tliat it becomes infinite, tlie phase becomes ferroelectric. This is tlie basis of ferroelectric liquid crystal displays (section C2.2.4.4). If tliere is an alternation in polarization direction between layers tlie phase can be ferrielectric or antiferroelectric. A smectic A phase foniied by chiral molecules is sometimes denoted SiiiA, altliough, due to the untilted symmetry of tlie phase, it is not itself chiral. This notation is strictly incorrect because tlie asterisk should be used to indicate the chirality of tlie phase and not tliat of tlie constituent molecules. [Pg.2549]

Because each lithium atom has one valence electron and each molecular orbital can hold two electrons, it follows that the lower half of the valence band (shown in color in Figure 5) is filled with electrons. The upper half of the band is empty. Electrons near the top of the filled MOs can readily jump to empty MOs only an infinitesimal distance above them. This is what happens when an electrical field is applied to the crystal the movement of electrons through delocalized MOs accounts for the electrical conductivity of lithium metal. [Pg.655]

In the above consideration it has been tacitly assumed that the charge carrier mobility docs not depend on the electric field. This is a good approximation for molecular crystals yet not for disordered systems in which transport occurs via hopping. Abkowitz et al. [37] have solved that problem for a field dependence of ft of the form p-po (FIFU) and trap-free SCL conduction. Their treatment predicts... [Pg.203]

Polyelectrolytes such as the ion exchange plastics form an interesting group of materials because of their ability to interact with water solutions. They have been used in medical applications involving the removal of heavy metal ions from the human body. They can be used to interact with external electric fields and change their physical properties drastically as is illustrated by the fact that some electrically active liquid crystals are polyelectrolytes of low molecular weight. [Pg.268]

One type of material that has transformed electronic displays is neither a solid nor a liquid, but something intermediate between the two. Liquid crystals are substances that flow like viscous liquids, but their molecules lie in a moderately orderly array, like those in a crystal. They are examples of a mesophase, an intermediate state of matter with the fluidity of a liquid and some of the molecular order of a solid. Liquid crystalline materials are finding many applications in the electronics industry because they are responsive to changes in temperature and electric fields. [Pg.325]

The response of liquid crystal molecular orientation to an electric field is another major characteristic utilised for many years in industrial applications [44] and more recently in studies of electrically-induced phase transitions [45]. The ability of the director to align along an external field again results from the electronic structure of the individual molecules. [Pg.13]

Liquid crystals (LCs) are organic liquids with long-range ordered structures. They have anisotropic optical and physical behaviors and are similar to crystal in electric field. They can be characterized by the long-range order of their molecular orientation. According to the shape and molecular direction, LCs can be sorted as four types nematic LC, smectic LC, cholesteric LC, and discotic LC, and their ideal models are shown in Fig. 23 [52,55]. [Pg.45]

J. G., De Lange, G. A. Molecular solutes in nematic liquid crystals orientational order and electric field gradients. Chem. Phys. Lett. 1983, 99, 271-274. [Pg.250]

Also there seems to be a certain time delay between photoreaction and complete recovery of the nematic phase. This problem is relevant to molecular mobility in liquid crystals as a function of temperature, rubbing condition, external electric field and most importantly, the type of liquid crystal. Research is now being undertaken on direct determination of molecular mobility by fluorescence technique. [Pg.219]

When the two wells are of similar energies, and the crystal structure allows, the above will no longer be the situation. We may then expect a number of consequences There may be a measurable displacement of the hydrogen between the two sites induced by such factors as a change in temperature, application of an electric field, and irradiation with light both tautomers may be present at symmetry-independent sites in the crystal different tautomers may be present in different crystal modifications and the presence of molecular substituents that do not directly affect the properties of the hydrogen bond may influence the tautomerism via the crystal structure. [Pg.159]

A simple calculation for urea by Spackman is instructive. Urea crystallizes in an acentric space group (it is a well-known nonlinear optical material), in which the symmetry axes of the molecules coincide with the two-fold axes of the space group. All molecules are lined up parallel to the tetragonal c axis. If the electric field is given by E, and the principal element of the diagonalized molecular polarizability tensor along the c axis by oc , the induced moment along the polar c axis is... [Pg.162]

Molecular crystals are among the most efficient second- and higher-harmonic generating materials. An external electric field E, upon interacting with a molecule, will induce a dipole moment p. If the field is strong, the response may not be linear, in which case the components of p can be developed in increasing powers of E as described by the expansion (i = 1, 2, 3)... [Pg.282]

In view of the potential technological importance of noncentrosymmetric organic crystals, several approaches have been evolved to artificially achieve noncentrosym-metry, which include electric field poling of polymers, self-assembly of molecular layers, Langmuir-Blodgett assembly of films and host-guest interaction in noncentrosymmetric hosts (Marder et al, 1994). Prediction and/or control of the three-dimensional structure of crystals, given only the information of molecular properties, however, remains difficult at present. [Pg.514]


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See also in sourсe #XX -- [ Pg.414 , Pg.415 , Pg.416 , Pg.417 , Pg.418 ]




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