Liquid crystalline polymeric chemical structure

The design and synthesis of new liquid crystalline polymeric materials endowed with intrinsc chirality deserve attention, as chirality can offer probes of the supermolecular structure and a tool for modulating specific responses of the polymers (1). The chemical transformation of preformed thermotropic polymers can add novel opportunities for the realization of various molecular architectures conventionally unfeasible and best suited for mesophase modification. 

The source of all carbon relevant to the present context is the feedstock of hydrocarbon molecules (aliphatic, aromatic, with and without heteroatoms). Figure 10 summarizes the possibilities for their conversion into black carbon. The chemical route comprises polymerization into aromatic hydrocarbons with final thermal dehydrogenation. This process often includes a liquid crystalline phase immediately before final solidification. In this phase large aromatic molecules can sclf-organizc into parallel stacks and form well-ordered precursors for graphitic structures with large planar graphene layers. This phase is referred to... 

Polymers with side anisodiametric groups modeling the molecular structure of low-molecular liquid crystals csm be obtained either through synthesis of monomers with liquid crystalline (mesogenic) groups with subsequent polymerization or throui chemical attachment of molecules of low-molecular liquid crystalline compounds to a polymer chain by way of polymer-analogous transformations. As can be inferred from the bulk of works dealing with this problem, at present, the first of these two methods is used in most cases. 

Conventional principles and methods concern the synthetic routes for macromo-lecular networks and the realization of the liquid crystalline state by mesogenic monomer tmits. Network chemistry has to consider the reactivity and functionality of the monomer tuiits. In most cases, this excludes ionic polymerization techniques and reduces utihzable methods to radical polymerization and polymer analog reactions for side chain networks, and to polycondensation or polyadditirai reactions for main chain elastomers. The chemistry of the crosslinking process and the chemical constitution of the crosslinker have to be adapted to the polymerization process. Applying photo-chemistry of suitable functional mmiomer units opens an additional, versatile pathway to build up the network structure. 

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