| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1326490 | Journal of Organometallic Chemistry | 2012 | 7 Pages |
The mixed ruthenium(II) complexes trans-[RuCl2(PPh3)2(bipy)] (1), trans-[RuCl2(PPh3)2(Me2bipy)](2), cis-[RuCl2(dcype)(bipy)](3), cis-[RuCl2(dcype)(Me2bipy)](4) (PPh3 = triphenylphosphine, dcype = 1,2-bis(dicyclohexylphosphino)ethane, bipy = 2,2′-bipyridine, Me2bipy = 4,4′-dimethyl-2,2′-bipyridine) were used as precursors to synthesize the associated vinylidene complexes. The complexes [RuCl(CCHPh)(PPh3)2(bipy)]PF6 (5), [RuCl(CCHPh)(PPh3)2(Me2bipy)]PF6 (6), [RuCl(CCHPh)(dcype)(bipy)]PF6 (7), [RuCl(CCHPh)(dcype)(bipy)]PF6 (8) were characterized and their spectral, electrochemical, photochemical and photophysical properties were examined. The emission assigned to the π–π∗ excited state from the vinylidene ligand is irradiation wavelength (340, 400, 430 nm) and solvent (CH2Cl2, CH3CN, EtOH/MeOH) dependent. The cyclic voltammograms of (6) and (7) show a reversible metal oxidation peak and two successive ligand reductions in the +1.5-(−0.64) V range. The reduction of the vinylidene leads to the formation of the acetylide complex, but due the hydrogen abstraction the process is irreversible. The studies described here suggest that for practical applications such as functional materials, nonlinear optics, building blocks and supramolecular photochemistry.
Graphical abstractThe mixed ruthenium(II) complexes were used as precursors to synthesize vinylidene complexes, which were characterized and their spectral, electrochemical, photochemical and photophysical properties were examined. The emission intensities obtained is surprising in view of the previous studies described for similar complexes, which suggest practical applications such as functional materials, nonlinear optics, building blocks and supramolecular photochemistry.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Ruthenium(II) complexes were used as precursors to synthesize vinylidene complexes. ► Electrochemical, photochemical and photophysical properties were examined. ► Formation of the acetylide complex was studied by electrochemistry and DFT. ► Emission intensities are surprising in view of the previous studies described.
