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Molecules with Multiple Chiral Centers02:25

Molecules with Multiple Chiral Centers

15.1K
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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Chirality02:25

Chirality

29.7K
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...
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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

7.0K
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...
7.0K
Molecules and Compounds02:38

Molecules and Compounds

69.0K
Atoms and Molecules
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Types of Signaling Molecules01:32

Types of Signaling Molecules

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In multicellular organisms, many molecules transmit signals between cells to pass information. These signals vary in complexity and include small peptides, nucleotides, steroids, fatty acid derivatives, and dissolved gases such as nitric oxide. Some signaling molecules diffuse through the plasma membrane to act locally between neighboring cells or travel long distances. Others remain attached to the cell surface, transmitting information to other cells only when they make contact. In some...
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Related Experiment Video

Updated: Feb 8, 2026

Cooling an Optically Trapped Ultracold Fermi Gas by Periodical Driving
11:21

Cooling an Optically Trapped Ultracold Fermi Gas by Periodical Driving

Published on: March 30, 2017

7.9K

Towards Ultracold Chiral Molecules.

Timur A Isaev1, Robert Berger2

  • 1National Research Center 'Kurchatov Institute' Petersburg Nuclear Physics Institute Orlova Roscha, 1, 188300 Gatchina, Russia.

Chimia
|June 27, 2018
PubMed
Summary

Laser cooling of molecules is now possible, enabling new research. This review covers laser cooling of polyatomic molecules and the potential for ultracold chiral molecules.

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Enzymatic Cascade Reactions for the Synthesis of Chiral Amino Alcohols from L-lysine

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Related Experiment Videos

Last Updated: Feb 8, 2026

Cooling an Optically Trapped Ultracold Fermi Gas by Periodical Driving
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Cooling an Optically Trapped Ultracold Fermi Gas by Periodical Driving

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Area of Science:

  • Quantum optics
  • Molecular physics
  • Laser cooling

Background:

  • Atoms are efficiently cooled using Doppler cooling via lasers.
  • Molecules were previously thought too complex for closed optical cooling loops.
  • Recent advancements have enabled laser cooling for certain diatomic and polyatomic molecules.

Purpose of the Study:

  • To review the current state of laser cooling for polyatomic molecules.
  • To discuss the potential for achieving ultracold chiral molecules.
  • To highlight recent experimental successes in molecular laser cooling.

Main Methods:

  • Utilizing Doppler cooling principles adapted for molecular systems.
  • Exploring molecular properties amenable to laser-driven cooling cycles.
  • Reviewing theoretical proposals and experimental implementations.

Main Results:

  • Laser cooling has been successfully demonstrated for diatomic molecules like SrF, YO, CaF, and YbF.
  • Recent experiments show successful laser cooling of polyatomic molecules, such as SrOH.
  • Classes of molecules suitable for laser cooling have been identified.

Conclusions:

  • Laser cooling of polyatomic molecules is an emerging field with significant potential.
  • Achieving ultracold chiral molecules is a promising future direction.
  • Continued research is expected to expand the applications of laser-cooled molecules.