French
DeutschPhanquinone
 | |
| Names | |
|---|---|
| Other names 4,7-phenanthroline-5,6-dione | |
| Identifiers | |
3D model (JSmol) | |
| ECHA InfoCard | 100.001.378 |
PubChem CID | |
CompTox Dashboard (EPA) | |
| |
| Properties | |
| C12H6N2O2 | |
| Molar mass | 210.192 g·mol−1 |
| Appearance | yellow solid |
| Melting point | 295 °C (563 °F; 568 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Phanquinone is an organic compound with the formula C12H6N2O2. It is derived by oxidation of 4,7-phenanthroline.
It has been investigated as both antiprotozoal agent and for its bactericidal activity .[1] It has an extensive role as a ligand in coordination chemistry.[2][3]
Related compounds
[edit]References
[edit]- ^ Mett H, Gyr K, Zak O, Vosbeck K (July 1984). "Duodeno-pancreatic secretions enhance bactericidal activity of antimicrobial drugs". Antimicrob. Agents Chemother. 26 (1): 35–8. doi:10.1128/aac.26.1.35. PMC 179912. PMID 6236746.
- ^ Eckert, Timothy S.; Bruice, Thomas C. (1983). "Chemical properties of phenanthrolinequinones and the mechanism of amine oxidation by o-quinones of medium redox potentials". Journal of the American Chemical Society. 105 (13): 4431–4441. doi:10.1021/ja00351a049.
- ^ Ksenofontov, Vadim; Gaspar, Ana B.; Niel, Virginie; Reiman, Sergey; Real, José A.; Gütlich, Philipp (2004). "On the Nature of the Plateau in Two-Step Dinuclear Spin-Crossover Complexes". Chemistry – A European Journal. 10 (5): 1291–1298. doi:10.1002/chem.200305275. PMID 15007819.
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