Abstract
2-Thienylamine (Hata) and 2-furfurylamine (Hafa) reacted with bis(acetylacetonato)palladium(II) [Pd(acac)2] in dichloromethane at room temperature to give Pd(acac)2(Hata) and Pd(acac)2(Hafa), respectively. In refluxing toluene the former amine gave [Pd(acac)(ata)]2, while with the latter no further reaction took place. In Pd(acac)2(Hata) and Pd(acac)2(Hafa) the amines were coordinated through the amino group, with one acac ligand as an OO chelate and the other γ-carbon bonded. X-ray analysis revealed that [Pd(acac)(ata)]2 was a dimer where the palladium atoms were bridged by deprotonated amino groups and coordinated with OO chelating acac ligands.
| Original language | English |
|---|---|
| Pages (from-to) | 1027-1030 |
| Number of pages | 4 |
| Journal | Polyhedron |
| Volume | 12 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - May 1993 |
| Externally published | Yes |
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Inorganic Chemistry
- Materials Chemistry