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Related Concept Videos

Photochemical Electrocyclic Reactions: Stereochemistry01:26

Photochemical Electrocyclic Reactions: Stereochemistry

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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Some cycloaddition reactions are activated by heat, while others are initiated by light. For example, a [2 + 2] cycloaddition between two ethylene molecules occurs only in the presence of light. It is photochemically allowed but thermally forbidden.
Photosystem I01:27

Photosystem I

Although structurally similar to photosystem II (PSII), photosystem I (PSI) is has a different electron supplier and electron acceptor.
Both these photosystems work in concert. An excited electron from PSII is relayed to PSI via an electron transport chain in the thylakoid membrane of the chloroplast, which is comprised of the carrier molecule plastoquinone, the dual-protein cytochrome complex, and plastocyanin. As electrons move between PSII and PSI, they lose energy and must be re-energized...

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Updated: Jul 1, 2026

Determination of the Photoisomerization Quantum Yield of a Hydrazone Photoswitch
09:33

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Published on: February 7, 2022

Mechanically Interlocked Indigo Photoswitches.

Alexander M Wilmshurst1, Taegeun Jo2, Rebecca L Kerridge1

  • 1School of Chemistry and Chemical Engineering, University of Southampton, Southampton, UK.

Angewandte Chemie (International Ed. in English)
|June 30, 2026
PubMed
Summary
This summary is machine-generated.

Researchers developed a new indigo photoswitch using constrained supramolecular interactions. This allows for red light control and significantly enhances stability, opening doors for advanced molecular machines and switching technologies.

Keywords:
photoswitchrotaxanesupramolecular chemistry

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Patterning via Optical Saturable Transitions - Fabrication and Characterization

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Area of Science:

  • Supramolecular Chemistry
  • Photochemistry
  • Materials Science

Background:

  • Photoswitches enable precise remote control of matter at the nanoscale.
  • Long-wavelength photoswitches are crucial for materials and biological applications, but few respond to red/near-infrared light.
  • Previous methods using intermolecular interactions to redshift photoswitch activation wavelengths are limited by bimolecularity, restricting their use in dilute or complex environments.

Purpose of the Study:

  • To develop a photoswitch with improved properties, specifically response to longer wavelengths and enhanced stability.
  • To overcome the limitations of previous supramolecular strategies for photoswitch optimization.
  • To explore the use of topologically constrained supramolecular interactions for photoswitch design.

Main Methods:

  • Incorporation of an indigo photoswitch into a [2]-rotaxane structure.
  • Utilizing topologically constrained supramolecular interactions to modify photoswitch properties.
  • Characterization of photoswitching behavior, thermal half-life, and metastable state population under irradiation.

Main Results:

  • Achieved photoswitching using 730 nm light, a significant red-shift.
  • Demonstrated a 100-fold increase in thermal half-life compared to previous methods.
  • Observed a doubling of the metastable state population under constant irradiation.
  • Exceeded previous supramolecular interaction strategies for enhancing thermal half-life by over 10-fold.

Conclusions:

  • Topologically constrained supramolecular interactions offer a powerful strategy for redshifting and fine-tuning molecular photoswitches.
  • This novel approach significantly improves photoswitch stability and response range.
  • The findings have broad implications for the design of molecular machines and applied switching technologies, particularly within the field of mechanically interlocked molecules.