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Chirality in Nature02:30

Chirality in Nature

17.9K
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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Chirality02:25

Chirality

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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...
31.8K
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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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...
7.3K
Standing Waves in a Cavity01:28

Standing Waves in a Cavity

1.6K
A household microwave and lasers are examples of standing electromagnetic waves in a cavity. When two conducting metal plates are placed parallel at the nodal planes, it creates a cavity where standing waves are formed. The cavity between the two planes is analogous to a stretched string held at the points x = 0 and x = L. Here, the distance 'L' between the two planes must be an integer multiple of half of the wavelength. The wavelengths that satisfy this condition are given by:
1.6K
Prochirality02:05

Prochirality

5.3K
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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Related Experiment Video

Updated: Mar 19, 2026

Automation of Mode Locking in a Nonlinear Polarization Rotation Fiber Laser through Output Polarization Measurements
14:18

Automation of Mode Locking in a Nonlinear Polarization Rotation Fiber Laser through Output Polarization Measurements

Published on: February 28, 2016

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Chiral modes and directional lasing at exceptional points.

Bo Peng1, Şahin Kaya Özdemir2, Matthias Liertzer3

  • 1Department of Electrical and Systems Engineering, Washington University, St. Louis, MO 63130;

Proceedings of the National Academy of Sciences of the United States of America
|June 9, 2016
PubMed
Summary
This summary is machine-generated.

Researchers demonstrate switchable unidirectional light emission in micro-resonators by controlling chirality near exceptional points (EPs). This breakthrough in chiral photonics enables precise light control for on-chip information processing.

Keywords:
asymmetric backscatteringchiral modesdirectional lasingexceptional pointswhispering-gallery-mode resonator

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Area of Science:

  • Photonics
  • Non-Hermitian Physics
  • Optics

Background:

  • Controlling light emission and propagation in micro/nanostructures is vital for on-chip information processing.
  • Exceptional points (EPs) are degeneracies in open systems where eigenvalues and eigenstates coalesce.
  • Whispering-gallery-mode (WGM) resonators are key microstructures for optical applications.

Purpose of the Study:

  • To demonstrate strong chirality and switchable light propagation direction in an optical system.
  • To explore the control of resonator modes and laser emission direction near EPs.
  • To pave the way for chiral photonics on a chip.

Main Methods:

  • Utilizing a fiber-coupled whispering-gallery-mode (WGM) resonator.
  • Dynamically controlling resonator mode chirality and laser emission direction.
  • Steering the optical system to exceptional points (EPs).

Main Results:

  • Achieved strong chirality and switchable unidirectional light emission near EPs.
  • Observed bidirectional emission away from EPs and unidirectional emission approaching EPs.
  • Demonstrated complete reversal of emission direction by transiting between EPs.

Conclusions:

  • Exceptional points offer a powerful mechanism for controlling light chirality and directionality.
  • This work exemplifies counterintuitive features of non-Hermitian physics.
  • The findings enable chiral photonics for advanced on-chip information processing.