1976
DOI: 10.1021/ja00437a020
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Mechanism of the quenching of the emission of substituted polypyridineruthenium(II) complexes by iron(III), chromium(III), and europium(III) ions

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Cited by 479 publications
(286 citation statements)
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“…For the complexes of the bpy and phen family it has been found that several excited state properties can be "tuned" by changing the nature of the central metal (Table 1) or the type of the ligands, or by appropriate substitutions on the ligand aromatic rings, Substitution of phen for bpy usually increases slightly the excited state lifetime and leaves almost unchanged the other excited state properties, but the introduction of different ligands may have profound consequences (4). Ligand substituents usually cause small changes in the excited state energy, but they can change significantly the excited state lifetime and the excited state reduction and oxidation potentialS (13,14). It is important to note that in these complexes the excitation causes a crossing of the redox potantials ( fig.…”
Section: Excited State Redox Properties Of Bipyridine and Phenanthrolmentioning
confidence: 99%
“…For the complexes of the bpy and phen family it has been found that several excited state properties can be "tuned" by changing the nature of the central metal (Table 1) or the type of the ligands, or by appropriate substitutions on the ligand aromatic rings, Substitution of phen for bpy usually increases slightly the excited state lifetime and leaves almost unchanged the other excited state properties, but the introduction of different ligands may have profound consequences (4). Ligand substituents usually cause small changes in the excited state energy, but they can change significantly the excited state lifetime and the excited state reduction and oxidation potentialS (13,14). It is important to note that in these complexes the excitation causes a crossing of the redox potantials ( fig.…”
Section: Excited State Redox Properties Of Bipyridine and Phenanthrolmentioning
confidence: 99%
“…Some red shift of X max to 473 and 501 nm is observed for Ru(terpy)^+ and Ru(TPTZ)^+ (terpy = 2,2',2"^terpyridine; TPTZ = 2,4,6-tri(2-pyridyl-s-triazine)) (26). These effects are very modest but they show that alternation of the ligand structure is a reasonable approach.…”
Section: -1 -1mentioning
confidence: 97%
“…It being a shame to waste all those potentially perfectly good solar photons, approaches must be taken to improve the absorption characteristics of the medium, especially to the red; there is no lack of chromophores + , substitution of phen (=1,10-phenanthroline) for bpy or substitution on the polypyridyl rings has little effect on X max or the shape of the visible absorption envelope (26,27). Some red shift of X max to 473 and 501 nm is observed for Ru(terpy)^+ and Ru(TPTZ)^+ (terpy = 2,2',2"^terpyridine; TPTZ = 2,4,6-tri(2-pyridyl-s-triazine)) (26).…”
Section: -1 -1mentioning
confidence: 99%
“…Platinum and palladium complexes with octaethylporphyrin (PtOEP 30, PdOEP 31) remain popular indicators due to their strong room temperature phosphorescence with a Taken from [141] b Nbpy0N-(6-aminohexyl)-4′-methyl-2,2′-bipyridine-4-carboxamide c L02,2-bipyridine (a) or 1,10-phenanthroline (b) and R0tert-butyl quantum yields of about 0.5 and 0.2, respectively, and long lifetimes under anoxic conditions (ca. 91 μs and ca.…”
Section: Metalloporphyrinsmentioning
confidence: 99%