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Related Concept Videos

Chirality02:25

Chirality

26.2K
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...
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Molecules with Multiple Chiral Centers02:25

Molecules with Multiple Chiral Centers

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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...
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Prochirality02:05

Prochirality

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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...
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Chirality in Nature02:30

Chirality in Nature

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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.
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Chirality at Nitrogen, Phosphorus, and Sulfur02:30

Chirality at Nitrogen, Phosphorus, and Sulfur

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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...
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Fischer Projections02:18

Fischer Projections

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Learning to draw Fischer projections of molecules and understanding their relevance plays a crucial role in the visual depiction of organic molecules. A Fischer projection is a two-dimensional projection on a planar surface to simplify the three-dimensional wedge–dash representation of molecules. This is especially helpful in the case of molecules with multiple chiral centers that can be difficult to draw. Here, all the bonds of interest are represented as horizontal or vertical lines.
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Related Experiment Video

Updated: Sep 29, 2025

Fabricating van der Waals Heterostructures with Precise Rotational Alignment
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Perovskite metasurfaces with large superstructural chirality.

Guankui Long1,2, Giorgio Adamo1,3, Jingyi Tian1,3

  • 1Centre for Disruptive Photonic Technologies, The Photonics Institute, Nanyang Technological University, 21 Nanyang Link, Singapore, 637371, Singapore.

Nature Communications
|March 24, 2022
PubMed
Summary
This summary is machine-generated.

Researchers developed novel all-dielectric perovskite metasurfaces for enhanced chirality. This planar nanostructure design overcomes limitations in hybrid perovskite synthesis, enabling advanced chiral photonic devices.

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Area of Science:

  • Materials Science
  • Nanotechnology
  • Optics

Background:

  • Synthesizing hybrid perovskites with significant chirality is challenging due to size mismatches and weak light interactions.
  • Existing methods struggle to achieve the desired chiral properties in perovskite materials.

Purpose of the Study:

  • To design and realize all-dielectric perovskite metasurfaces with giant superstructural chirality.
  • To overcome the limitations of previous hybrid perovskite synthesis attempts.
  • To establish a spectral link between near- and far-field chirality.

Main Methods:

  • Adoption of a planar nanostructure design for perovskite metasurfaces.
  • Tuning electric and magnetic multipole moments of resonant chiral metamolecules.
  • Utilizing simulations to predict performance of larger area metasurfaces.

Main Results:

  • Achieved giant superstructural chirality in all-dielectric perovskite metasurfaces.
  • Demonstrated a direct spectral correspondence between near- and far-field chirality.
  • Obtained a large anisotropy factor of 0.49 and circular dichroism of 6350 mdeg.
  • Simulations indicate potential for even higher optical activity in larger metasurfaces.

Conclusions:

  • The planar nanostructure design effectively overcomes limitations in synthesizing chiral perovskites.
  • Engineered perovskite metasurfaces show significant potential for high optical activity.
  • This approach paves the way for advanced perovskite-based chiral photonic, optoelectronic, and spintronic devices.