Phanquinone

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Phanquinone
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Names
Other names
4,7-phenanthroline-5,6-dione
Identifiers
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3D model (JSmol)
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365810
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  • InChI=1S/C12H6N2O2/c15-11-9-7(3-1-5-13-9)8-4-2-6-14-10(8)12(11)16/h1-6H
    Key: VLPADTBFADIFKG-UHFFFAOYSA-N
  • O=C3c1ncccc1c2c(nccc2)C3=O
Properties
C12H6N2O2
Molar mass 210.192 g·mol−1
Appearance yellow solid
Melting point 295 °C (563 °F; 568 K)
Hazards
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

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Phanquinone is an organic compound with the formula Page Module:Chem2/styles.css has no content.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]

References

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  1. ^ Page Module:Citation/CS1/styles.css has no content.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.
  2. ^ Page Module:Citation/CS1/styles.css has no content.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. Bibcode:1983JAChS.105.4431E. doi:10.1021/ja00351a049.
  3. ^ Page Module:Citation/CS1/styles.css has no content.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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