Related Experiment Video
Updated: Oct 11, 2025

10:35
Novel Techniques for Observing Structural Dynamics of Photoresponsive Liquid Crystals
Published on: May 29, 2018
8.9K
Rods in a lyotropic chromonic liquid crystal: emergence of chirality, symmetry-breaking alignment, and caged angular
Sophie Ettinger1, Clarissa F Dietrich2, Chandan K Mishra3
1Department of Physics and Astronomy, University of Pennsylvania, Philadelphia, PA, 19104, USA. asophie@sas.upenn.edu.
Soft Matter
|December 1, 2021
Summary
Rod-like particles in lyotropic chromonic liquid crystals (LCLCs) exhibit unique orientations and chiral director configurations. The particle
Area of Science:
- Soft Matter Physics
- Liquid Crystal Science
- Materials Science
Background:
- Lyotropic chromonic liquid crystals (LCLCs) exhibit low energy cost for twist distortion.
- This property enables novel mirror-symmetry breaking director configurations.
- Asymmetric rod-like particles introduce complex possibilities in aligned LCLCs.
Purpose of the Study:
- Investigate director configuration around rod-like particles in LCLCs.
- Determine equilibrium orientation and angular diffusion of these particles.
- Understand how particle aspect ratio and orientation influence LCLC behavior.
Main Methods:
- Video microscopy to observe particle behavior.
- Polarized optical video-microscopy for director configuration analysis.
- Landau-de Gennes numerical modeling for theoretical validation.
Main Results:
- Two-thirds of rods adopt an angled equilibrium orientation, decreasing with aspect ratio.
- One-third of rods align with the far-field director.
- Distinct chiral director configurations (LMP for angled, TLMP for aligned rods) were observed.
Conclusions:
- LCLC's low twist elastic constant promotes chiral configurations that alter particle orientation.
- Particle aspect ratio influences equilibrium orientation and angular confinement.
- Chiral director configurations are intrinsically linked to particle shape and alignment.
Related Concept Videos
Chirality in Nature
14.6K
Chirality is the most intriguing yet essential facet of nature, governing life’s biochemical processes and precision. It can be observed from a snail shell pattern in a macroscopic world to an amino acid, the minutest building block of life. Most of the snails around the world have right-coiled shells because of the intrinsic chirality in their genes. All the amino acids present in the human body exist in an enantiomerically pure state, except for glycine - the sole achiral amino acid.
14.6K
Stereoisomerism of Cyclic Compounds
9.8K
In this lesson, we delve into the role of ring conformation and its stability, which determines the spatial arrangement and, consequently, the molecular symmetry and stereoisomerism of cyclic compounds. 1,2-Dimethylcyclohexane is used as a case study to evaluate the possible number of stereoisomers. Here, given the multiple (n = 2) chiral centers, there are 2n = 4 possible configurations that lack a plane of symmetry, as the ring skeleton exists in a non-planar chair conformation. In addition,...
9.8K
Properties of Enantiomers and Optical Activity
18.9K
It is essential to understand the difference between chiral and achiral interactions and the implications thereof in optical activity and their applications. Just as our feet, which are chiral, interact uniquely with chiral objects, such as a pair of shoes, but identically with achiral socks, enantiomers of a molecule exhibit different properties only when they interact with other chiral media. An example of a significant implication from this facet is the phenomenon known as optical activity,...
18.9K
Chirality
26.7K
Chirality is a term that describes the lack of mirror symmetry in an object. In other words, chiral objects cannot be superposed on their mirror images. For example, our feet are chiral, as the mirror image of the left foot, the right foot, cannot be superposed on the left foot.
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
26.7K
Molecules with Multiple Chiral Centers
13.6K
Molecules that possess multiple chiral centers can afford a large number of stereoisomers. For instance, while some molecules like 2-butanol have one chiral center, defined as a tetrahedral carbon atom with four different substituents attached, several molecules like butane-2,3-diol have multiple chiral centers. A simple formula to predict the number of stereoisomers possible for a molecule with n chiral centers is 2n. However, there can be a lower number where some of the stereoisomers are...
13.6K
Stereoisomerism
12.6K
Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
12.6K

