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Cholesteric optical properties

Werbowyj and Gray (79) examined the relationships between the cholesteric pitch and optical properties of HPC in water, CH3COOH and CH3OH. The reciproc pitch varied as the third power of the HPC concentration. Optical rotatory dispersion results show HPC has a right-handed superhelicoidal structure regardless of structure. As will be discussea below, a change in solvent can reverse the handedness of other cellulose derivatives. [Pg.265]

Several unique optical properties arise from helical structures of cholesteric liquid crystals. [Pg.94]

These unique optical properties of cholesteric liquid crystals have been investigated... [Pg.94]

Electronic displays make use of the fact that the orientation of the molecules in liquid crystals changes in the presence of an electric field. This reorientation causes a change in their optical properties, making them opaque or transparent, and hence forming a pattern on a screen. Cholesteric liquid crystals are also of interest because the helical structure unwinds slightly as the temperature is changed. Because the twist of the helical structure affects the optical properties of the liquid crystal, these... [Pg.374]

The systematic synthesis of non amphiphilic l.c.-side chain polymers and detailed physico-chemical investigations are discussed. The phase behavior and structure ofnematic, cholesteric and smectic polymers are described. Their optical properties and the state of order of cholesteric and nematic polymers are analysed in comparison to conventional low molar mass liquid crystals. The phase transition into the glassy state and optical characterization of the anisotropic glasses having liquid crystalline structures are examined. [Pg.99]

The realization of nematic side chain polymers implies the possibility of the existence of cholesteric side chain polymers, presuming the mesogenic molecules, which are linked to the backbone, are chiral. For these polymers it is of interest, whether the polymer fixation influences the helical twist and therefore the optical properties of the cholesteric phase. This will be discussed in 2.3.2.2. [Pg.135]

Polymers of cholesteric type attract particular interest among LC polymers — inspired by the unique optical properties of cholesterics 142). [Pg.220]

The macromolecular nature provides an interesting feature of LC polymeric cholesterics, namely the possibility of obtaining monochromic films. Thus for polymeric liquid crystals the helix pitch is practically not altered with temperature below Tg, when a cholesteric phase is frozen in a glassy matrix (Fig. 23a). This implies that fast cooling of polymeric films from a mesomorphic state (shown with arrows) fixes their optical properties, which makes it possible to use them at ordinary temperatures as selective monochromic reflectors. On the other hand, such polymeric films display the extraordinary polarizing properties of cholesterics, i.e. the different absorption... [Pg.224]

In cholesteric structures there is also alignment, but the direction of alignment rotates on a screw axis normal to the direction of alignment (Figure 16.2). This spiraling is responsible for unique optical properties. [Pg.168]

Liquid-crystalline solutions and melts of cellulosic polymers are often colored due to the selective reflection of visible fight, originating from the cholesteric helical periodicity. As a typical example, hydroxypropyl cellulose (HPC) is known to exhibit this optical property in aqueous solutions at polymer concentrations of 50-70 wt%. The aqueous solution system is also known to show an LCST-type of phase diagram and therefore becomes turbid at an elevated temperature [184]. [Pg.135]

Experimentally, the cholesteric structure parameters, i.e., pitch and handedness, can be derived from the optical properties of the phase and very specially from its so-called selective reflection. This most striking phenomenon is the reflection of one component of circular polarized radiation in a spectral interval around that wavelength which within the medium matches the cholesteric pitch, i.e. XrIh = i when n denotes the... [Pg.337]

The cholesteric mesophases have Interesting optical properties. [Pg.143]

Other equally remarkable optical properties are associated with the selective reflection. At normal incidence, the reflected light is circularly polarized one circular component is totally reflected, while the other passes through unchanged. Also, quite contrary to what is found in normal substances, the reflected wave has the same sense of circular polarization as that of the incident wave. This is an important difference between the nature of the optical rotation of normal substances and of cholesteric liquid crystals. While the more familiar cases of optical rotation have their origin in the selective absorption of one circularly polarized component of the light, the form optical rotation of the twisted structure in cholesteric liquid crystals originates in the selective reflection of one circularly polarized component of the light. [Pg.48]

Fig. 7. Optical properties of right-handed cholesteric liquid crystals... Fig. 7. Optical properties of right-handed cholesteric liquid crystals...
However, there is a structure consistent with both the required space group and the optical properties. The gyroid surface, which occurs frequently in lipid-water systems, provides such a possibility. If we assume that cholesterol skeletons form rod-like infinite helices, this structure represents an effective three-dimensional packing of such helices. Thus, the rods form a body-centered arrangement as shown in Fig. 5.5. In this structure, there is a helical twist between the rods, in addition to the cholesteric twist within each rod. The h)rperbolic structure is a consequence of the chirality of the esters, which induces torsion into the packing arrangement. A racemic mixture does not exhibit this phase natural cholesteric esters contain a single enantiomer only. [Pg.212]

In this liquid crystal phase, the molecules have non-symmetrical carbon atoms and thus lose mirror symmetry. Otherwise optically active molecules are doped into host nematogenic molecules to induce the chiral liquid crystals. The liquid crystals consisting of such molecules show a helical structure. The most important chiral liquid crystal is the cholesteric liquid crystals. As discussed in Section 1.2, the cholesteric liquid crystal was the first discovered liquid crystal and is an important member of the liquid crystal family. In some of the literature, it is denoted as the N phase, the chiral nematic liquid crystal. As a convention, the asterisk is used in the nomenclature of liquid crystals to mean the chiral phase. Cholesteric liquid crystals have beautiful and interesting optical properties, e.g., the selective reflection of circularly polarized light, significant optical rotation, circular dichroism, etc. [Pg.19]

As mentioned in Chapter 1, cholesteric liquid crystals have a helical structure. The helical structure results in unique optical properties, such as selective reflection, circular dichroism, drastic optical activity, and electro-optic effects. [Pg.315]


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See also in sourсe #XX -- [ Pg.9 ]




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