Abstract
N-heterocyclic carbene (NHC)-Pd(II) bonds are recognized as rather robust bonds to equip palladium(II) centers with decent stability and stereoelectronic tunability. In this report, the authentic carbene-Pd(II) bonds in N-ammonium- and sulfonate-functionalized NHC complexes were activated, and NHC ligand exchange was triggered to afford four well-defined, sulfobetaine-type, zwitterionic heterobiscarbene complexes. Combined experimental studies and density functional theory calculations indicated that electrostatic interactions play a minimal role in the energy of this reaction; instead, the exchange appears to be driven primarily by the precipitation of the resulting zwitterionic complexes.
| Original language | English |
|---|---|
| Pages (from-to) | 21806-21809 |
| Number of pages | 4 |
| Journal | Inorganic Chemistry |
| Volume | 63 |
| Issue number | 46 |
| DOIs | |
| Publication status | Published - 18 Nov 2024 |
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