Spatially controllable surface chirality at the nanoscale

We demonstrate a mechanical approach for manipulating surface chirality at nanoscopic length scales. We use an atomic-force microscope to scribe a step pattern, which is chiral in two dimensions, into a polymer-coated substrate, and control chiral strength by varying the steps’ length-to-width ratio R. We determine the chiral strength by coating the surface with a liquid crystal and measuring its rotation on applying an electric field. The chiral strength vs. R is nonmonotonic: zero for R=1, then reaching a maximum, and tending to zero as R→∞. Our results demonstrate that chiral handedness and strength can be precisely controlled mechanically on nanoscopic length scales

Oligomers as Triggers for Responsive Liquid Crystals

We report an investigation of the influence of aqueous solutions of amphiphilic oligomers on the ordering of micrometer-thick films of thermotropic liquid crystals (LCs), thus addressing the gap in knowledge arising from previous studies of the interactions of monomeric and polymeric amphiphiles with LCs. Specifically, we synthesized amphiphilic oligomers (with decyl hydrophobic and pentaethylene glycol hydrophilic domains) in monomer, dimer, and trimer forms, and incubated aqueous solutions of the oligomers against nematic films of 4'-pentyl-4-biphenylcarbonitrile (5CB). All amphiphilic oligomers caused sequential surface-driven orientational (planar to homeotropic) and then bulk phase transitions (nematic to isotropic) with dynamics depending strongly on the degree of oligomerization. The dynamics of the orientational transitions accelerated from monomer to trimer, consistent with the effects of an increase in adsorption free energy. The mechanism underlying the orientational transition, however, involved a decrease in anchoring energy and not change in the easy axis of the LC. In contrast, the rate of the phase transition induced by absorption of oligomers into the LC decreased from monomer to trimer, suggesting that constraints on configurational degrees of freedom influence the absorption free energies of the oligomers. Interestingly, the oligomer-induced transition from the nematic to isotropic phase of 5CB was observed to nucleate at the aqueous-5CB interface, consistent with surface-induced disorder underlying the above-reported decrease in anchoring energy caused by the oligomers. Finally, we provided proof-of-concept experiments of the triggering of LCs using a trimeric amphiphile that is photocleaved by UV illumination into monomeric fragments. Overall, our results provide insight into the rational design of oligomers that can be used as triggers to create responsive LCs.11Nsciescopu

Amphiphile-Induced Phase Transition of Liquid Crystals at Aqueous Interfaces

Monolayer assemblies of amphiphiles at planar interfaces between thermotropic liquid crystals (LCs) and an aqueous phase can give rise to configurational transitions of the underlying LCs. A common assumption has been that a reconfiguration of the LC phase is caused by an interdigitation of the hydrophobic tails of amphiphiles with the molecules of the LC at the interface. A different mechanism is discovered here, whereby reorientation of the LC systems is shown to occur through lowering of the orientation-dependent surface energy of the LC due to formation of a thin isotropic layer at the aqueous interface. Using a combination of atomistic molecular dynamics simulations and experiments, we demonstrate that a monolayer of specific amphiphiles at an aqueous interface can cause a local nematic-to-isotropic phase transition of the LC by disturbing the antiparallel configuration of the LC molecules. These results provide new insights into the interfacial, molecular-level organization of LCs that can be exploited for rational design of biological sensors and responsive systems.11Nsciescopu

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Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/74420/1/j.1360-0443.1990.tb03079.x.pd