Abstract
Activation and cleavage of chemical bonds are pivotal for the chemical recovery of plastics back to value-added products. The gem-dimethyl motif in plastics enhances physicochemical properties via steric reinforcement of quaternary carbon centers, yet its inherent chemical inertness concurrently impedes the degradative process. We demonstrate a photocatalytic relay bond cleavage protocol for gem-dimethyl-type plastic degradation, in which chlorine radical from photoexcited ferric trichloride enables the activation of inert C(sp3)–H bonds in gem-dimethyl motifs followed by two successive C–C bond cleavages via divergent mechanistic pathways. Mechanistic investigations reveal that the first C(sp3)–C(sp3) bond undergoes homolytic cleavage via radical-type β-scission, and then the second C(sp3)–C(sp2) bond undergoes heterolytic cleavage via ionic-type O–O bond dissociation inducing a 1,2-aryl migration. This efficient protocol achieves effective degradation for gem-dimethyl-type plastics, offering an economically sustainable strategy for plastic waste valorization.
| Original language | English |
|---|---|
| Pages (from-to) | 2230-2239 |
| Number of pages | 10 |
| Journal | Science Bulletin |
| Volume | 71 |
| Issue number | 9 |
| DOIs | |
| State | Published - 15 May 2026 |
Keywords
- Degradation
- Photocatalyzed
- Polycarbonate-based plastics
- Relay cleavage
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