Abstract
The potentially tridentate ligand 2,6-bis[(3-methylimidazolium-1-yl)methyl]pyridine dibromide reacts readily with silver(I) oxide in dichloromethane or dimethylsulfoxide to give a dinuclear silver(I)-carbene complex that was isolated as the tetrafluoroborate salt. Single crystal X-ray crystallography shows that each silver(l) ion is bridged by two ligands bonding through the carbene donors. Treatment of the silver(l) complex with suitable palladium(II) precursors gave the complexes PdCl[(CNC)BF4 and [PdMe(CNC]BF4 (CNC = 2,6-bis[(3-methylimidazolin-2-yliden-1-yl)methyl]pyridine), in which the pyridyl and both carbene moieties are coordinated to a single palladium(II). The palladium(11) complexes have been fully characterised, including X-ray crystallography, and exhibit good activities in the Heck coupling reaction of 4-bromoacetophenone and n-butyl acrylate. (C) 2002 Elsevier Science B.V. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 116-125 |
| Journal | Inorganica Chimica Acta |
| Volume | 327 |
| Issue number | n/a |
| DOIs | |
| Publication status | Published - 2002 |
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