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Liquid‐crystalline elastomers with cholesteric and chiral smectic C<sup>*</sup> phases
79
Citations
30
References
1989
Year
Macromolecular ChemistryEngineeringLiquid Crystalline ElastomerChemistrySoft MatterPolymersMacromolecular EngineeringSoluble CopolymersHydrosilylation ReactionCrystal FormationPolymer ChemistryMaterials ScienceSynthetic MacromoleculeCrystal MaterialBiopolymersLiquid‐crystalline ElastomersCrystallographySupramolecular PolymerBiomolecular EngineeringMacromolecular SciencePolymer Science
Abstract A series of 9 new chiral and crosslinkable liquid‐crystalline copolymers were synthesized and transformed into liquid‐crystalline elastomers by crosslinking using a hydrosilylation reaction. Both the soluble copolymers and the elastomers show cholesteric, smectic A and chiral smectic C * phases, which are not affected by the crosslinking procedure. First measurements show that the helical superstructure of elastomers with cholesteric and chiral smectic C * phases can be reversibly untwisted by stretching. Thereby a cholesteric structure can be transformed into a nematic structure and a chiral smectic C * structure into a smectic C one.
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