Thermotropic nematic phases

Liquid crystal gold nanopartides that exhibit a thermotropic nematic phase in the bulk have been reported recently (Figure 8.28). 

For X-Y = 8-hydroxyquinolato ( = 0) and X-Y= 1,10-phenanthroline ( =1), the complexes were non-meso-morphic. However, when X-Y = acac (n = 0), a material with a monotropic SmA phase resulted (Cr 83 (SmA 68) I) and when X-Y = 2,2 -bipyridine (n= [BF4] counterion), a material with an enantiotropic nematic phase was produced (Cr 146 N 158 I) related complexes with PF6 or SbF6 anions were non-mesomorphic. These are further, rare examples of ionic materials showing a thermotropic nematic phase. 

Lyotropic nematic phases were first reported by Lawson and Flautt (62) for mixtures of Cg and Cio alkyl sulfates, together with their corresponding alcohols in water. They are somewhat less common than the mesophases discussed so far. When they do form, they occur at the boundary between an isotropic micellar phase (LQ and the hexagonal phase (Li/HQ, or between Li and the lamellar phase (Li/L ). As their name implies, they have a similar micellar order to that of the molecules in a thermotropic nematic phase. This long-range micellar orientational and translational order is lower than in the other lyotropic phases described above. Like the thermotropic phases, they are of low viscosity and can be aligned in a magnetic field. It is possible to identify nematic phases optically because of their characteristic schlieren optical texture. 

Finally it shall be mentioned that until now no inverse nematic phases could be detected. Also the existence of nematic phases in non-polar solvents could not be proven for any studied system. Thus it is not yet possible to replace the thermotropic nematic phases in displays by lyotropic systems because lyotropic nematics caimot be orientated in an electric field with low voltages due to the rather high conductivity of the water solvent compared to non-polar organic compounds. 

Hamley I W, Garnett S, Luckhurst G R, Roskilly S J, Pedersen J S, Richardson R M and Seddon J M 1996 Orientational ordering in the nematic phase of a thermotropic liquid crystal A small angle neutron scattering study J. Chem. Phys. 104 10 046-54... 

The separation of Hquid crystals as the concentration of ceUulose increases above a critical value (30%) is mosdy because of the higher combinatorial entropy of mixing of the conformationaHy extended ceUulosic chains in the ordered phase. The critical concentration depends on solvent and temperature, and has been estimated from the polymer chain conformation using lattice and virial theories of nematic ordering (102—107). The side-chain substituents govern solubiHty, and if sufficiently bulky and flexible can yield a thermotropic mesophase in an accessible temperature range. AcetoxypropylceUulose [96420-45-8], prepared by acetylating HPC, was the first reported thermotropic ceUulosic (108), and numerous other heavily substituted esters and ethers of hydroxyalkyl ceUuloses also form equUibrium chiral nematic phases, even at ambient temperatures. 

The prime requirement for the formation of a thermotropic liquid crystal is an anisotropy in the molecular shape. It is to be expected, therefore, that disc-like molecules as well as rod-like molecules should exhibit liquid crystal behaviour. Indeed this possibility was appreciated many years ago by Vorlander [56] although it was not until relatively recently that the first examples of discotic liquid crystals were reported by Chandrasekhar et al. [57]. It is now recognised that discotic molecules can form a variety of columnar mesophases as well as nematic and chiral nematic phases [58]. 

Many technological applications of liquid crystals, as in electro-optic display devices, are based on multicomponent mixtures. Such systems offer a route to the desired material properties which cannot be achieved simultaneously for single component systems. Mixtures also tend to exhibit a richer phase behaviour than pure systems with features such as re-entrant nematic phases [3] and nematic-nematic transitions possible. In this section, we describe simulations which have been used to study mixtures of thermotropic calamitic mesogens. 

The study of the cholesteric mesophases obtained by doping thermotropic nematics with chiral, nonracemic compounds, has lead to relevant information about the stereochemistry of the dopants. Chiral interactions change the structure of the phase and therefore molecular chirality can be mapped onto an achiral (nematic) phase to yield a superstructural phase chirality. In 1984 Sol-ladie and Zimmermann published the first review summarizing the state of the art at that time.52 Later on, several review articles updated this subject.53-55... 

Liquid crystals have been used as an ordered medium for small solutes since the first observation of 1H NMR spectrum of benzene in a nematic phase by Saupe and Englert.190 The NMR spectra of solutes disolved in thermotropics... 

Discotic LC are formed by disk-like molecules with aromatic cores and side chains that are either hydrophobic (i.e., thermotropic) or hydrophilic (i.e., lyotropic). The discotic nematic (No) phase behaves like a normal nematic phase formed by rod-like molecules, and the disk-like molecules are oriented with their short molecular axes parallel to the director but show no positional order. More ordered columnar phases are commonly formed by thermotropic discotics. The two-dimensional structure can pack the columns into a hexagonal or rectangular columnar phase, while within the columns, disks can be... 

Note 1 The adjective thermotropic describes a change of phase with a change of temperature. Thermotropic may also be used to qualify types of mesophase (e.g., thermotropic nematic). 

The aggregates created by amphiphiles are usually spherical (as in the case of micelles), but may also be disc-like (bicelles), rodlike, or biaxial (all three micelle axes are distinct) (Zana, 2008). These anisotropic self-assembled nanostructures can then order themselves in much the same way as liquid crystals do, forming large-scale versions of all the thermotropic phases (such as a nematic phase of rod-shaped micelles). 

The development is reviewed of liquid-crystalline polymers whose mesophase formation derives from the nature of the chemical units in the main chain. The emphasis lies primarily on highly aromatic condensation polymers and their applications. The general properties of nematic phases formed by such polymers are surveyed and some chemical structures capable of producing nematic phases are classified in relation to their ability to form lyotropic and thermotropic systems. The synthesis, properties, physical structure and applications of two of the most important lyotropic systems and of a range of potentially important thermotropic polymers are discussed with particular reference to the production and use of fibres, films and anisotropic mouldings. 

Academic and industrial interest in liquid-crystalline polymers of the main-chain type has been stimulated by certain special properties shared by lyotropic and thermotropic systems that exhibit a nematic phase. Although these special properties affect both the processing into fibres and other shaped articles and the physical behaviour of the products, the product behaviour is at least partly attributable to the novel processing behaviour. 

Both lyotropic and thermotropic liquid-crystalline synthetic polymers have been widely studied. Aromatic polyamides constitute the most important class forming liquid-crystalline solutions the solvents are either powerfully protonating acids such as 100% sulphuric acid, chloro-, fluoro- or methane-sulphonic acid, and anhydrous hydrogen fluoride, or aprotic dipolar solvents such as dimethyl acetamide containing a small percentage, usually 2-5 %, of a salt such as lithium chloride or calcium chloride. Such solutions constitute a nematic phase within certain limits. Some criteria for formation of a nematic instead of an isotropic phase are ... 

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