| Literature DB >> 24841757 |
Yiqun Bai1, Reza Abbasi, Chenxuan Wang, Nicholas L Abbott.
Abstract
The orientations of liquid crystals (LCs) anchored on monolayers formed from mixtures of chiral versus achiral molecules were compared. Changes in the enantiomeric excess of mixed monolayers of chiral dipeptides gave rise to continuous changes in the orientations of nematic LCs, allowing arbitrary tuning of the azimuthal orientations of LCs over a range of ≈100°. In contrast, the same LCs exhibited discontinuous changes in orientation on surfaces presenting mixtures of achiral molecules. These striking differences in the anchoring of LCs on surfaces presenting chiral versus achiral molecules provide insights into the molecular origins of ordering transitions of LCs, and provide new principles based on chiral monolayers for the rational design of surfaces that permit continuous tuning of the orientations of LCs.Entities:
Keywords: chirality; interfaces; liquid crystals; peptides; supramolecular organization
Mesh:
Year: 2014 PMID: 24841757 PMCID: PMC4241358 DOI: 10.1002/anie.201402770
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336