Chiral columnar phase

Compound 114d possesses significantly lower transition temperatures (Scheme 60) due to the branched side chains [126]. A columnar phase is present even below room temperature. At 14 °C, anew chiral columnar phase was observed while above 111 °C, an achiral columnar rectangular phase was observed. The spiral-pattern texture of 114d in the chiral Col mesophase is shown in Fig. 17. 

For a detailed discussion of the frustrated phases, such as blue, TGB, and chiral columnar phases, see the chapters by Bock, Crooker, Kitzerow, and Pieranski. 

Apart from the triphenylene mentioned in Section 11.2, one other case has been reported where a chiral columnar phase structure manifests itself in an asymmetric texture 2,3,9,10,16,17,23,24-octakis-(5-3,7-dimethyloctyloxy)-phthalocyanine exhibits two columnar phases above room temperature [8], [14]. The one at the higher temperature has a rectangular column lattice, the other a hexagonal one. When cooled quickly from the isotropic liquid, left-handed spirals appear in the flower-like texture of the highly ordered room temperature phase (Figure 11.8). X-ray and circular dichroism measurements indicate a helical superstructure with a pitch of 55 A (a 16 molecules). It seems very probable that in this case the molecules are weakly tilted and that the tilt direction spirals around the column axis, especially because the phase at higher temperatures is rectangular and therefore most probably tilted as well. 

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]. 

Extensive studies have been conducted to investigate the formation of chiral columns or helical superstructures in chiral and nonchiral disk- [53], star- [54, 55], and board-shaped [56] molecules. However, spontaneous deracemization has never been unambiguously demonstrated in discotic columnar phases consisting of nonchiral or racemic molecules. We recently observed clear evidence showing chiral resolution in a disk-like molecules with a dibenzo[g,p]chrysene core [57]. 

The preparation of a cubic phase with supramolecular chirality was achieved using a branched folic acid derivative incorporating glutamic acid residues (Fig. 11) as the source of chirality [93]. The pterin rings of folic acid residues are able to form a cyclic tetramer as a result of two hydrogen bonds between the components. Depending on the number of carbon atoms in the alkyl substituents, the compounds form columnar phases over a wide temperature range, and for 8 and 9 form cubic phases at temperatures above 130 °C. Addition of sodium triflate stabilises the cubic phase for 7, and the salt is incorporated into the other mesophases. It was implied that the cation resides between stacked tetramers. Supramolecular chirality is expressed for both the columnar and the cubic phases, as revealed by vari-... 

Just as chiral induction can be realised in discotic liquid crystals, it can also be realised in assemblies of disc-like molecules or disc-like aggregates. As far as molecules are concerned, C3-symmetrical trisamides (Fig. 15), which actually exhibit discotic liquid crystalline phases, also form chiral columnar stacks through it-it interactions when dissolved in apolar solvents, which are depicted schematically in Fig. 15 [121]. An achiral compound of this type (15) exhibits no optical activity in dodecane, but when the compound is dissolved in the chiral CR)-(-)-2,6-dimelhyloctanc significant Cotton effects (only slightly less intense than those observed in a chiral derivative) are detected. The chiral disc-like trisamide 16 can also be used as a dopant at concentrations as low as 2.5% to induce supramolecular chirality in the stacks of achiral compound. In this case, the presence of the additional hydrogen... 

The liquid crystal melt, which comes into being at the glass-rubber transition or at the crystal-melt transition, may have several phase states (Mesophases) one or more smectic melt phases, a nematic phase and sometimes a chiral or cholesteric phase the final phase will be the isotropic liquid phase, if no previous decomposition takes place. All mesophase transitions are thermodynamically real first order effects, in contradistinction to the glass-rubber transition. A schematic representation of some characteristic liquid crystal phase structures is shown in Fig. 6.13, where also so-called columnar phases formed from disclike molecules is given. 

However, more remarkable was the discovery that in alkane solvents, large, orrfiometallated macrocyclic complexes of palladium shown in Figure 92 would form lyotropic columnar phases [171], These remarkable materials have been shown to form columnar hexagonal phases and, in suitable solvents, lyotropic nematic phases derived from columnar organization. Further, in certain non-mesomorphic examples, mesophases can be induced by the addition of an electron acceptor such as trinitrofluorenone chiral phases are introduced when the acceptor is resolved 2 -(2,4,5,7-tetranitro-9-fluorenylideneaminoxy)propionic acid (know as TAPA). 

Spontaneous polarisation can also be observed for chiral discotic metallomesogens forming columnar mesophases, when the chiral molecules are tilted with respect to the column axis. The tilt induces a dipole moment within the plane of the molecule. A net macroscopic polarisation can be obtained for rectangular columnar phases with Cz or P2i symmetry. Serrano and Sierra reported on ferroelectric switching in the columnar mesophase for chiral /3-diketonate complexes (Figure 2.52). ... 

Compound 43 was found to exhibit a chiral nematic phase (see the texture in Fig. 48), hexagonal disordered columnar (see Fig. 49) and rectangular disordered columnar phases, in the sequence g 5.4 Col d 30 Col 102.3 N 107.7 °C Iso Liq [94]. Thus the increase in the number density of the meso-gens bound to the central scaffold transforms the situation from the octamers 41 and 42, which exhibit calamitic phases, to one where the hexadecamer 43 exhibits columnar phases. However, the formation of columnar phases when the dendrimer possesses rod-like mesogenic groups is not easy to vi-... 

Recently Ribeiro et al. [65] reported on the synthesis and characterization of a variety of tolanes that had optically active sulfinate groups. Some of these compounds, see 23, were found to possess a phase that exhibited oily-streak textures typical of chiral nematic phases and also defect pattern associated with columnar phases (the earlier photomicrograph Plate 6 for 14P1M7 is similar). 

In addition, these complexes, except 49a and 50a, form lyotropic columnar (oblique) and nematic phases when dissolved in linear, apolar organic solvents (alkanes) over wide temperature and concentration ranges. Interestingly, for some of them, 49b-c, an unexpected transition between two lyotropic nematic phases has been observed, for which a model has recently be proposed [93]. As for 48, formation of lyotropic nematic and columnar mesophases is also extended by n-n interactions with electron-acceptors, such as TNF, in apolar solvents (pentadecane). Induction of chiral nematic phases by charge transfer interactions, in a ternary mixture (49b/alkane/TAPA TAPA is 2-(2,4,5,7-tetranitro-9-fluorenylideneaminooxy)-propionic acid and is used (and is available commercially) enantiomerically pure), has recently been demonstrated for the first time [94], and opens new perspective for producing chiral nematic phase of disc-like compounds. 

In a similar approach, Saigo et al. have prepared a chiral columnar LC structure [2] using the same benzoic acid derivative and a chiral amino alcohol (Fig. 2.13) [64-66]. The columnar phase could be photopolymerized and powder X-ray... 

Lyotropic cellulosics mostly exhibit chiral nematic phases, although columnar phases have also been observed. The molecules in the thermotropic state also form chiral nematic order, but it is sometimes possible to align them in such a way that a helicoidal structure of a chiral nematic is excluded. Upon relaxation they show banded textures. Overviews on lyotropic LC cellulosics are... 

A basic understanding of the structure and behavior of liquid-crystalline cellulosics has yet to evolve. From a conceptual point of view, the chirality of the cellulosic chain is most sensitively expressed in the super-molecular structure of the cholesteric phase, which may be described by the twisting power or the pitch. At present, no information is available about domains or domain sizes (correlation lengths) of supermo-lecular structures. The chirality in the columnar phases has not been addressed at all. The principal problem, i.e., how does chirality on a molecular or conformational level promote chirality on the supermolecular level, has not been solved. If this correlation were known, it would enable the determination of the conformation of cellulosic chains in the mesomorphic phase and the development of models for the polymer-solvent interactions for lyotropic systems. On the other hand, direct probing of this interaction would provide a big leap towards an understanding of lyotropic phases. 

Just as chiral induction can be realized in discotic liquid crystals, so it can in assemblies of disc-like molecules or disc-like aggregates. As far as molecules are concerned, C3-symmetrical fm-amides (Fig. 6), which exhibit discotic liquid-crystalline phases, also form chiral columnar stacks through n-n interactions when dissolved in apolar solvents,which are depicted schematically in... 

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