Abstract
The unique combination of a divalent organolanthanide fragment, Cp∗2Yb, with bipyrimidine (bipym) and a palladium bis-alkyl fragment, PdMe2, allows the rapid formation and stabilization of a PdIV tris-alkyl moiety after oxidative addition with MeI. The crucial role of the organolanthanide fragment is demonstrated by the substitution of bipym by the 4,5,9,10-tetraazaphenanthrene ligand, which drastically modifies the electronic structure and tunes the stability of the PdIV species.
| Original language | English |
|---|---|
| Pages (from-to) | 10633-10636 |
| Number of pages | 4 |
| Journal | Journal of the American Chemical Society |
| Volume | 139 |
| Issue number | 31 |
| DOIs | |
| Publication status | Published - 9 Aug 2017 |
| Externally published | Yes |
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