Chiral induction in thioester and oxoester liquid crystals by dispersed carbon nanotubes

Multi-walled carbon nanotubes were dispersed at low concentrations into various achiral liquid crystals having either a thioester or oxoester linkage group in the core. The presence of the carbon nanotubes resulted in chiral signatures being observed in the liquid crystals, including an electroclinic effect (a rotation of the liquid crystal director perpendicular to, and linear in, an applied electric field) in both the nematic and smectic A phases, and a macroscopic helical twist of the liquid crystal director in the nematic phase. For both experiments the chiral signatures for the thioester liquid crystals were found to be an order of magnitude larger than those of the oxoesters. We speculate that the much larger strength of the thioester's chiral properties is a result of stronger non-covalent interactions between the liquid crystal molecule and carbon nanotube.