Liquid crystal materials flexible amphiphilics

Polymerization of LB films, or deposition of LB films on polymers, offers the opportunity to impart to LB films a higher degree of mechanical integrity. However, preliminary work in this direction shows a conflict between the chainlike primary structure of the polymer and the well-organized supramo-lecular structure [15]. One possible solution may be the insertion of flexible spacers between the main chain polymer and the side chain amphiphile, a route also employed in liquid crystal polymers. These materials belong to an interesting class of two-dimensional polymers, of which there are few examples. These toughening techniques may eventually be applied to stabilize other self-assembled microstructures, such as vesicles, membranes, and microemulsions. 

As their name implies, liquid crystals are materials whose structures and properties are intermediate between those of isotropic liquids and crystalline solids (2). They can be of two primary types. Thermotropic liquid crystalline phases are formed at temperatures intermediate between those at which the crystalline and isotropic liquid phases of a mesogenic compound exist. Substances which exhibit thermotropic phases are generally rod- or disc-like in shape, and contain flexible substituents attached to a relatively rigid molecular core. Lyotropic liquid crystalline phases are formed by amphiphilic molecules (e.g. surfactants) in the presence of small amounts of water or other polar solvent. In general, the constituent molecules in a liquid crystal possess orientational order reminiscent of that found in the crystalline phase, yet retain some degree of the fluidity associated with the isotropic liquid phase. 

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