Abstract |
Carbon monoxide (CO) has recently been shown to impart beneficial effects in mammalian physiology and considerable research attention is now being directed toward metal-carbonyl complexes as a means of delivering CO to biological targets. Two ruthenium carbonyl complexes, namely trans-dicarbonyldichlorido(4,5-diazafluoren-9-one-κ(2)N,N')ruthenium(II), [RuCl2(C11H6N2O)(CO)2], (1), and fac-tricarbonyldichlorido(4,5-diazafluoren-9-one-κN)ruthenium(II), [RuCl2(C11H6N2O)(CO)3], (2), have been isolated and structurally characterized. In the case of complex (1), the trans-directing effect of the CO ligands allows bidentate coordination of the 4,5-diazafluoren-9-one (dafo) ligand despite a larger bite distance between the N-donor atoms. In complex (2), the cis disposition of two chloride ligands restricts the ability of the dafo molecule to bind ruthenium in a bidentate fashion. Both complexes exhibit well defined (1)H NMR spectra confirming the diamagnetic ground state of Ru(II) and display a strong absorption band around 300 nm in the UV.
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Authors | Jorge Jimenez, Indranil Chakraborty, Pradip Mascharak |
Journal | Acta crystallographica. Section C, Structural chemistry
(Acta Crystallogr C Struct Chem)
Vol. 71
Issue Pt 11
Pg. 965-8
(Nov 2015)
ISSN: 2053-2296 [Electronic] England |
PMID | 26524168
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, Non-P.H.S.)
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Chemical References |
- Coordination Complexes
- Fluorenes
- Ligands
- Ruthenium Compounds
- fac-tricarbonyldichlorido(4,5-diazafluoren-9-one-kappaN)ruthenium(II)
- trans-dicarbonyldichlorido(4,5-diazafluoren-9-one-kappa(2)N,N')ruthenium(II)
- Ruthenium
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Topics |
- Coordination Complexes
(chemical synthesis, chemistry)
- Crystallography, X-Ray
- Fluorenes
(chemistry)
- Hydrogen Bonding
- Ligands
- Magnetic Resonance Spectroscopy
- Quantum Theory
- Ruthenium
(chemistry)
- Ruthenium Compounds
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