Exhaustive Catalytic ortho-Alkoxylation of Azobenzenes: Flexible Access to Functionally Diverse Yellow-Light-Responsive Photoswitches
Author:
Affiliation:
1. Department of Pharmacy, Ludwig-Maximilians University, Butenandtstrasse 5-13, Munich 81377, Germany
Funder
Deutsche Forschungsgemeinschaft
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c02214
Reference39 articles.
1. Advances and opportunities in the exciting world of azobenzenes
2. Hole Catalysis as a General Mechanism for Efficient and Wavelength-Independent Z → E Azobenzene Isomerization
3. Efficient Electrocatalytic Switching of Azoheteroarenes in the Condensed Phases
4. SAXS measurements of azobenzene lipid vesicles reveal buffer-dependent photoswitching and quantitative Z→E isomerisation by X-rays
5. Photoswitches: From Molecules to Materials
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3. Centennial Isomers: A Unique Fluorinated Azobenzene Macrocyclus with Dual Stability Over 120 Years;Advanced Functional Materials;2024-02-13
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