Abstract
Ruthenium 1,2-naphthoquinone-1-oxime (1-nqoH) complexes cis, cis-[Ru(η2-N(O)C10H6O)2(CO)(vpy)] (3) and trans, cis-[Ru(η2-N(O)C10H6O)2(CO)(vpy)] (4) were synthesised by substituted decarbonylation reactions of dicarbonyl complexes cis, cis-[Ru(η2-N(O)C10H6O)2(CO)2] (1) and trans, cis-[Ru(η2-N(O)C10H6O)2(CO)2] (2), respectively. In addition, a dipyridine product trans, trans-[Ru(η2-N(O)C10H6O)2(vpy)2] (5) was also obtained in both reaction routes as the result of a ligand rearrangement during the substitution process of the second carbonyl ligand. The molecular structure of 3 was established by X-ray analysis. Co-polymerisation reactions were conducted on 3 with styrene as the co-monomer. The metal-containing moieties maintain the coordination geometry of the starting monomer 3 on the carbon-backbone chain.
Original language | English |
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Pages (from-to) | 231-238 |
Number of pages | 8 |
Journal | Inorganica Chimica Acta |
Volume | 312 |
Issue number | 1-2 |
DOIs | |
Publication status | Published - 29 Jan 2001 |
Externally published | Yes |
Keywords
- 1,2-Naphthoquinone-1-oxime complexes
- Copolymerisation
- Ruthenium complexes
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Inorganic Chemistry
- Materials Chemistry