Liquid crystals molecular tilt

Also the above-described SmQ phase was object of molecular simulation studies by using the molecule shown in Fig. 10.42 [99]. Figure 10.43 shows the structure of the SmQ phase, which is also known as the r l phase. This structure is based on a model according to Levelut et al. (Fig. 10.40 in [100]), in which the local liquid crystal molecular alignment direction is tilted in respect to the layers of smectic blocks. In the case of a 45° tilt, this leads to a cubic phase with a threefold symmetry. 

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. 

The compounds crystallise in noncentrosymmetric space groups namely PI, P2i, C2, and P2i2i2i (but with priority of P2i) due to the chirality of the molecules. Most of the compounds have a tilted layer structure in the crystalline state. The tilt angle of the long molecular axes with respect to the layer normal in the crystal phase of the compounds is also presented in Table 18. Some compounds show larger tilt angles in the crystalline state than in the smectic phase. In the following only the crystal structures of some selected chiral liquid crystals will be discussed. 

The earliest approach to explain tubule formation was developed by de Gen-nes.168 He pointed out that, in a bilayer membrane of chiral molecules in the Lp/ phase, symmetry allows the material to have a net electric dipole moment in the bilayer plane, like a chiral smectic-C liquid crystal.169 In other words, the material is ferroelectric, with a spontaneous electrostatic polarization P per unit area in the bilayer plane, perpendicular to the axis of molecular tilt. (Note that this argument depends on the chirality of the molecules, but it does not depend on the chiral elastic properties of the membrane. For that reason, we discuss it in this section, rather than with the chiral elastic models in the following sections.)... 

The second issue concerns the anisotropy of the membrane. The models presented in this section all assume that the membrane has the symmetry of a chiral smectic-C liquid crystal, so that the only anisotropy in the membrane plane comes from the direction of the molecular tilt. With this assumption, the membrane has a twofold rotational symmetry about an axis in the membrane plane, perpendicular to the tilt direction. It is possible that a membrane... 

It is also possible that a membrane might have an even lower symmetry than a chiral smectic-C liquid crystal in particular, it might lose the twofold rotational symmetry. This would occur if the molecular tilt defines one orientation in the membrane plane and the direction of one-dimensional chains defines another orientation. In that case, the free energy would take a form similar to Eq. (5) but with additional elastic constants favoring curvature. The argument for tubule formation presented above would still apply, but it would become more mathematically complex because of the extra elastic constants. As an approximation, we can suppose that there is one principal direction of elastic anisotropy, with some slight perturbations about the ideal twofold symmetry. In that approximation, we can use the results presented above, with 4) representing the orientation of the principal elastic anisotropy. 

A very different model of tubules with tilt variations was developed by Selinger et al.132,186 Instead of thermal fluctuations, these authors consider the possibility of systematic modulations in the molecular tilt direction. The concept of systematic modulations in tubules is motivated by modulated structures in chiral liquid crystals. Bulk chiral liquid crystals form cholesteric phases, with a helical twist in the molecular director, and thin films of chiral smectic-C liquid crystals form striped phases, with periodic arrays of defect lines.176 To determine whether tubules can form analogous structures, these authors generalize the free-energy of Eq. (5) to consider the expression... 

Figure 7.1. Categories of smectic liquid crystals. From Smectic Liquid Crystals, Textures and Structures, Gray, G.W. and Goodby, J.W.G. 1984 (Leonard Hill, Glasgow). (Reproduced by kind permission of the authors and publishers.) Side elevation and plan representation of molecular ordering in each of the smectic modifications. Triangles or arrows are used to represent tilt direction.

Figure 7.3. Schematic diagram to illustrate the mechanism of ferroelectric liquid crystals. It is supposed that the molecules have a structure which encourages a tilt as in (a). It is further supposed that (in this simple illustration) there exists an electric dipole at right angles to the molecular axis which points out of the paper in (a), , and into the paper in (6), . It is supposed that the configuration shown in (a) represents the lower energy state.

Liquid crystals can be in the smectic, nematic, or isotropic states. In the smectic liquid crystalline state there is a long-range order in the direction of the long axis of the molecules. These molecules may be in single- or bilayer conformation, have molecular axis normal or tilted to the plane of the layer, and frozen or melted chains. In the nematic liquid crystalline state the molecules are aligned side by side but not in specific layers. The isotropic liquid crystalline state is more or less a liquid state, but where clusters with short-range order persist (Small, 1986, pp. 49-51). 

Cholesteric liquid crystals are similar to smectic liquid crystals in that mesogenic molecules form layers. However, in the latter case molecules lie in two-dimensional layers with the long axes parallel to one another and perpendicular or at a uniform tilt angle to the plane of the layer. In the former molecules lie in a layer with one-dimensional nematic order and the direction of orientation of the molecules rotates by a small constant angle from one layer to the next. The displacement occurs about an axis of torsion, Z, which is normal to the planes. The distance between the two layers with molecular orientation differing by 360° is called the cholesteric pitch or simply the pitch. This model for the supermolecular structure in cholesteric liquid crystals was proposed by de Vries in 1951 long after cholesteric liquid crystals had been discovered. All of the optical features of the cholesteric liquid crystals can be explained with the structure proposed by de Vries and are described below. 

In a chiral smectic (Sc ) phase, the tilt angle is the same within a layer, but the tilt direction processes and traces a helical path through a stack of layers (Figure 43). It has been demonstrated that when such a helix is completely unwound, as in a surface stabilized ferroelectric liquid crystal cell, then changing the tilt of the molecules fi om +0 to —0 by alternating the direction of an applied field results in a substantial electro-optic effect, which has the features of veiy fast switching (%1 - lOps), high contrast and bistability [87]. The smectic A phase of chiral molecules may also exhibit an electro-optic effect, this arises due to molecular tilt fluctuations which transition is approached, which are combined with a... 

Figure 6.41. The dependence of the tilt angle 20 on temperature for (a) the small molecular mass ferroelectric liquid crystals LI, L2 and L3 and (b) their polymer counterparts PI, P2 and P3. (From Sekiya et al., 1993. Reproduced by permission of Taylor Francis, )...

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