Résumé
The first systematic mechanism study of C-F reductive elimination from a transition metal complex is described. C-F bond formation from three different Pd(IV) fluoride complexes was mechanistically evaluated. The experimental data suggest that reductive elimination occurs from cationic Pd(IV) fluoride complexes via a dissociative mechanism. The ancillary pyridyl-sulfonamide ligand plays a crucial role for C-F reductive elimination, likely due to a K 3 coordination mode, in which an oxygen atom of the sulfonyl group coordinates to Pd. The pyridyl-sulfonamide can support Pd(IV) and has the appropriate geometry and electronic structure to induce reductive elimination.
| langue originale | Anglais |
|---|---|
| Pages (de - à) | 3793-3807 |
| Nombre de pages | 15 |
| journal | Journal of the American Chemical Society |
| Volume | 132 |
| Numéro de publication | 11 |
| Les DOIs | |
| état | Publié - 24 mars 2010 |
| Modification externe | Oui |
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