Green-Light Responsive Perylene Bisimides for Atom-Economic Thiol Generation and Click-Ligation

Novel methylthiophene/benzo­[b]­thiophene perylene bisimide thiol-precursors that would generate thiols via a green-light-induced (λexc = 530 nm, φre = 0.33) photorearrangement are presented herein. The “no-wash”, photoreleased thiols thus enabled a subsequent thiol–ene click ligation with electron-...

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Veröffentlicht in:Organic letters 2023-02, Vol.25 (5), p.872-876
Hauptverfasser: Zhang, Fang, Zhang, Zhiwei, Deng, Long, Guo, Huichao, Xia, Tong, Mao, Wenxuan, Zhang, Junji
Format: Artikel
Sprache:eng
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Zusammenfassung:Novel methylthiophene/benzo­[b]­thiophene perylene bisimide thiol-precursors that would generate thiols via a green-light-induced (λexc = 530 nm, φre = 0.33) photorearrangement are presented herein. The “no-wash”, photoreleased thiols thus enabled a subsequent thiol–ene click ligation with electron-deficient substrates. Moreover, by virtue of the intrinsic fluorescence evolution from the rearrangement of perylene bisimide scaffolds, the whole process of thiol formation could be self-reported, further potentiating themselves with application versatilities.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.3c00101