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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 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.
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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.
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Isomerism in Complexes
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The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
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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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Pillar[5]arene-Based Visual Planar Chirality Switches with Variable Color Expression.

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|October 21, 2025
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Summary
This summary is machine-generated.

Researchers developed dynamic chiral switches (P5N-R and P5N-S) that change color in response to external stimuli like solvents and guest molecules, enabling new responsive chiral materials.

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Area of Science:

  • Supramolecular Chemistry
  • Materials Science
  • Organic Chemistry

Background:

  • Developing molecular systems with controllable chirality and macroscopic property changes is challenging.
  • Existing dynamic chirality platforms and molecular designs are limited.

Purpose of the Study:

  • To create novel chirality-controlled switches with reversible modulation of planar chirality.
  • To establish a correlation between molecular conformation, guest inclusion, and macroscopic color changes.

Main Methods:

  • Synthesis of two chirality-controlled switches, P5N-R and P5N-S.
  • Investigating the reversible modulation of planar chirality using solvents, temperature, and guest molecules.
  • Analyzing conformational changes and their impact on intramolecular hydrogen bonding and electronic properties.

Main Results:

  • P5N-R and P5N-S exhibit reversible chirality control and color changes.
  • Guest inclusion promotes a pillar conformation (pR-form), while exclusion favors a folded conformation (pS-form).
  • Conformational changes alter intramolecular hydrogen bonds, affecting electron donation and causing distinct color changes.

Conclusions:

  • A new strategy for constructing dynamic chiral switches with macroscopic property changes has been demonstrated.
  • These switches offer a promising avenue for developing advanced, responsive chiral materials.
  • The findings have significant implications for molecular-level chirality control systems.