Abstract
A homologous series of linear, mononuclear gold(I) phosphine/phosphido-borohydride complexes, encompassing [Au(PR3)2]+ 1, [Au(PR3)(PR2BH3)] 2 and [Au(PR2BH3)2]– 3 (R = tBu, Ad), has been prepared and structurally characterised. Strong intramolecular dispersion interactions are evident in the complexes with Ad-substituted ligands, which adopt eclipsed conformations in the solid state exclusively while there is no clear preference for the tBu-substituted analogues. Despite the disparate donor properties of the phosphine and phosphido-borohydride ligands, there are no statistically significant differences in Au–P bond length (~2.33 Å) across the series. This difference is, however, manifested in the redox characteristics of the gold(I) complexes, which are more readily oxidised in the order 1 < 2 < 3.
| Original language | English |
|---|---|
| Pages (from-to) | 1-17 |
| Number of pages | 17 |
| Journal | European Journal of Inorganic Chemistry |
| Early online date | 11 Jun 2025 |
| DOIs | |
| Publication status | E-pub ahead of print - 11 Jun 2025 |
Keywords
- homologous series
- mononuclear gold
- intramolecular dispersion interactions
- Ad-substituted ligands
- gold(I) complexes
- Gold
- phosphane ligands
- coordination chemistry
- P ligands
- solid‐state structures
- solid-state structures