Photoinduced Synthesis of C3-Arylated 7-Aminocoumarins with Aryl Iodides
C3-Arylated 7-aminocoumarins have found extensive applications as fluorescent probes and laser dyes. In this study, we report a photoinduced synthesis of 3-aryl-7-diethylaminocoumarins using readily available aryl iodides. The proposed mechanism involves a photoinduced single electron transfer process between aryl iodides and 7-diethylaminocoumarins in their first singlet excited states (S<sub>1</sub>), leading to the formation of aryl radicals that are crucial for the C3-arylation reaction. The resulting C3-arylated 7-diethylaminocoumarins exhibit distinct fluorescence quantum yields in the solid state and in solution, which are significantly influenced by the electronic properties of the C3-aryl groups.
Authors
- Jin‐Hong Lin (ORCID: https://orcid.org/0000-0002-7000-9540)
- Xiaojun Tang (ORCID: https://orcid.org/0000-0001-8757-0927)
- Rui Wang (ORCID: https://orcid.org/0000-0003-3830-4133)
- Ting Lin (ORCID: https://orcid.org/0000-0002-5145-5561)
- W. G. Cao
- Wen-Jiao Zhang
- Zhikun Zhang
Institutions
- Shanghai University (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2025-12-24
- DOI
- https://doi.org/10.1021/acs.joc.5c02101
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00