Catalyst-FreeThiol–yne Nucleophilic PhotoclickChemistry
Abstract X-yne nucleophilic addition reactions are essential and powerful tools in a range of synthetic routes for realizing functional and stimuli-responsive materials. Unfortunately, the lack of spatiotemporal control and the requirement for catalyst addition in these reactions limit their full potential in synthetic and materials-based applications, including in light-driven 3D printing. Herein, we close this critical gap and exploit a spirothiopyran (STP) photoswitch as a synthon for photoinduced and catalyst-free thiol–yne click reactions, an important class of X-yne click chemistries. We further employ our photoswitch-based entity for rapid and facile postpolymerization modification as well as photopolymerization under very mild and aerobic conditions.
Authors
- Christopher Barner‐Kowollik (ORCID: https://orcid.org/0000-0002-6745-0570)
- Linh Duy Thai (ORCID: https://orcid.org/0000-0003-2256-0423)
- S. Roth (ORCID: https://orcid.org/0000-0002-3921-0959)
- Frank Kirschhöfer (ORCID: https://orcid.org/0000-0002-7873-7614)
Institutions
- Karlsruhe Institute of Technology (DE)
- Queensland University of Technology (AU)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-08-14
- DOI
- https://doi.org/10.1021/jacs.6c09543
- Primary Topic
- Photochromic and Fluorescence Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Alexander von Humboldt-Stiftung