Abstract
Pincer-ligated phosphoranides constitute a relatively underexplored subclass of main-group compounds whose distinctive structural and electronic properties are now attracting renewed interest. In this study, we report the synthesis, full characterization, and novel photoreactivity of O,N,O-pincer ligated phosphoranide anions. Upon visible-light irradiation, these species engage in single-electron transfer (SET) processes with various aryl halides, enabling the formation of C–P and C–C bonds. A combination of electrochemical studies and TD-DFT calculations supports a mechanism involving the formation of electron donor–acceptor (EDA) complexes, followed by light-induced SET and radical recombination. These findings introduce these phosphoranides as a versatile platform for photochemical transformations and underscore the broader potential of main-group frameworks in light-driven redox chemistry.
| Original language | English |
|---|---|
| Pages (from-to) | 579-584 |
| Number of pages | 6 |
| Journal | Chemical Science |
| Volume | 17 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 7 Jan 2026 |
| Externally published | Yes |
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