All Visible Light Switch Based on the Dimethyldihydropyrene Photochromic Core
Margot Jacquet1, Lucas M Uriarte2, Frédéric Lafolet3
1Université Grenoble Alpes, DCM UMR 5250, F-38000 Grenoble, France.
The Journal of Physical Chemistry Letters
|March 18, 2020
Summary
New photoswitchable compounds operate using visible light. These dimethyldihydropyrene (DHP)/cyclophanediene (CPD) systems show reversible switching for potential biological and electronic applications.
Area of Science:
- Photochemistry
- Supramolecular Chemistry
- Materials Science
Background:
- Photochromic compounds enable light-controlled molecular switching.
- Visible light-responsive systems are desirable for biological and electronic applications.
Purpose of the Study:
- To synthesize and characterize novel photoswitchable compounds operating under visible light.
- To investigate the photochromic behavior of dimethyldihydropyrene (DHP)/cyclophanediene (CPD) systems linked to bipyridine or ruthenium complexes.
Main Methods:
- Spectroscopic studies (UV-Vis absorption, NMR) to monitor isomerization.
- Computational studies (DFT) to understand electronic properties and reaction mechanisms.
- Synthesis of DHP/CPD coupled with bpy or Ru(bpy)3 moieties via a pyridinium bridge.
Main Results:
- Two novel photoswitchable compounds were successfully synthesized.
- The DHP to CPD isomerization (red light, >630 nm) and CPD to DHP conversion (blue light, 460 nm) were confirmed.
- Reversible and unambiguous photochromic switching was achieved using visible light.
Conclusions:
- The developed all-visible photoswitchable systems offer precise control over molecular states.
- These compounds show promise for applications in biological imaging, sensing, and molecular electronics.
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