Rational Molecular Design of Germole-Fused Dithienylethenes with Tunable Photochromic Response, Reaction Pathway, and
Tony Ho-Ching Fung1, Nathan Man-Wai Wu1, Ziyong Chen1
1Institute of Molecular Functional Materials, State Key Laboratory of Synthetic Chemistry and Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, 999077, P. R. China.
New photoswitchable organogermanium compounds featuring germole-fused dithienylethenes were synthesized. These stable and efficient photoswitches demonstrate excellent thermal stability and high photochromic performance for practical applications.
Area of Science:
- Materials Science
- Organic Chemistry
- Photochemistry
Background:
- Photoswitchable molecules are crucial for advanced optical applications.
- Dithienylethenes are well-known photochromic compounds.
- Organogermanium compounds offer unique electronic properties.
Purpose of the Study:
- To design and synthesize novel photoswitchable organogermanium compounds.
- To investigate the photochromic properties of germole-fused dithienylethenes.
- To evaluate their potential as stable and efficient photoswitches.
Main Methods:
- Synthesis of germole-fused dithienylethene derivatives.
- Photochromic performance evaluation in solution and thin films.
- Assessment of photostability, thermal stability, and switching efficiency.
Main Results:
- Successful synthesis of new photoswitchable organogermanium compounds.
- Tunable optical band gaps leading to distinct photochromic responses.
- Robust photofatigue resistance (12 cycles) and excellent thermal irreversibility (half-life up to 33 days at 100 °C).
- High photoswitching efficiencies with up to 85% conversion at photostationary state.
Conclusions:
- Germole-fused dithienylethenes represent a promising class of photoswitchable materials.
- These compounds exhibit superior stability and efficiency for photoswitching applications.
- The rational design allows for fine-tuning of photochromic properties.
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