Acid derivatives, chiral nematics

Liquid Crystalline Structures. In certain ceUular organeUes, deoxyribonucleic acid (DNA) occurs in a concentrated form. Striking similarities between the optical properties derived from the underlying supramolecular organization of the concentrated DNA phases and those observed in chiral nematic textures have been described (36). Concentrated aqueous solutions of nucleic acids exhibit a chiral nematic texture in vitro (29,37). 

On the other hand, literature data show [16] that different cellulose derivatives which form liquid crystalline solutions in organic solvents may also form cholesteric thermotropic phases in the absence of a solvent—with spontaneous molecular orientation and cholesteric reflection, such as 2-acetoxypropyl cellulose, 2-hydroxypropyl cellulose, the trifluoroacetate ester of hydroxypropyl cellulose, the propanoate ester of hydroxypropyl cellulose, the benzoate ester of hydroxypropyl cellulose, 2-ethoxypropyl cellulose, acetoacetoxypropyl cellulose, trifluoroacetoxypropyl cellulose, the phenylac-etate and 3-phenylpropionate of hydroxypropyl cellulose, phenylacetoxy, 4-methoxy-phenylacetoxy, p-tolylacetoxy cellulose, trimethylsilyl cellulose, trialkyl cellulose, cellulose trialkanoate, the trialkyl ester of (tri-o-carboxymethyl) cellulose, 6-o-a-(l-methylnaphthalene)-2,3-o-pentyl cellulose, etc. Moreover, the suspensions of cellulose crystallites spontaneously form the chiral nematic phase. The formation of mesophase suspension of cellulose crystalHtes varies from one type of cellulose to another, being influenced, in the formation of the chiral nematic phase, by the mineral acid selected... 

Compound 120 shows a short monotropic chiral nematic and smectic A phase, whilst 121 shows a short enantiotropic chiral nematic and a monotropic smectic A phase. From this it may be concluded that the lactic acid derived ( )-2-oxypropanoy-loxy moiety is not particularly suited to sustaining liquid crystal phases this may either be partly due to poor conjugation between the liquid crystalline cores or because of the non-linear nature of molecules. 

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). 

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