Related Experiment Video
Updated: Feb 28, 2026

07:03
Measuring Magnetically-Tuned Ferroelectric Polarization in Liquid Crystals
Published on: August 15, 2018
9.3K
Straight round the twist: frustration and chirality in smectics-A
Elisabetta A Matsumoto1, Randall D Kamien2, Gareth P Alexander3
1School of Physics, Georgia Institute of Technology, 837 State Street, Atlanta, GA 30309, USA.
Interface Focus
|June 21, 2017
Summary
Frustration in chiral smectic liquid crystals can lead to complex defect textures. Highly chiral systems favor a hierarchical helical nanofilament phase over the standard twist grain boundary phase.
Area of Science:
- Condensed Matter Physics
- Materials Science
- Liquid Crystal Physics
Background:
- Frustration in condensed matter systems drives order and complexity.
- In smectic liquid crystals, frustration between chirality and layer spacing creates defect-rich textures.
- The twist grain boundary (TGB) phase is typically the ground state for chiral type II smectics.
Purpose of the Study:
- To investigate various ground states of the chiral Landau-de Gennes free energy in smectic liquid crystals.
- To understand the influence of high chirality on phase stability.
Main Methods:
- Theoretical study of the chiral Landau-de Gennes free energy.
- Analysis of different ground states and their stability.
Main Results:
- The standard theory predicts the TGB phase as the ground state for chiral type II smectics.
- For highly chiral systems, the hierarchical helical nanofilament (HHNF) phase emerges.
- The HHNF phase is found to be stable and can supersede the TGB phase in highly chiral regimes.
Conclusions:
- Chirality plays a critical role in determining the ground state of smectic liquid crystals.
- The hierarchical helical nanofilament phase represents a stable alternative ground state in highly chiral smectics.
- This finding expands our understanding of defect formation and phase behavior in chiral liquid crystals.
Related Concept Videos
Chirality at Nitrogen, Phosphorus, and Sulfur
7.1K
Chirality is most prevalent in carbon-based tetrahedral compounds, but this important facet of molecular symmetry extends to sp3-hybridized nitrogen, phosphorus and sulfur centers, including trivalent molecules with lone pairs. Here, the lone pair behaves as a functional group in addition to the other three substituents to form an analogous tetrahedral center that can be chiral.
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
7.1K
Chirality
30.6K
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...
30.6K
Prochirality
5.2K
The concept of prochirality leads to the nomenclature of the individual faces of a molecule and plays a crucial role in the enantioselective reaction. It is a concept where two or more achiral molecules react to produce chiral products. A typical process is the reaction of an achiral ketone to generate a chiral alcohol. Here, the achiral reactant reacts with an achiral reducing agent, sodium borohydride, to generate an equimolar mixture of the chiral enantiomers of the product. For example, an...
5.2K
Molecules with Multiple Chiral Centers
15.5K
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...
15.5K
Chirality in Nature
17.4K
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.
17.4K
Naming Enantiomers
26.9K
The naming of enantiomers employs the Cahn–Ingold–Prelog rules that involve assigning priorities to different substituent groups at a chiral center. Each enantiomer, being a distinct molecule, is assigned a unique name by the Cahn–Ingold–Prelog (CIP) rules, also called the R–S system. The prefix R- or S- attached to the chiral centers in an enantiomer is dependent on the spatial arrangement of the four substituents on the chiral center. The R–S system essentially comprises three...
26.9K

