SUPRAMOLECULAR RU AND OR OS COMPLEXES OF TRIS(BIPYRIDINE) BRIDGING LIGANDS - SYNTHESES, ABSORPTION-SPECTRA, LUMINESCENCE PROPERTIES, ELECTROCHEMICAL-BEHAVIOR, INTERCOMPONENT ENERGY, AND ELECTRON-TRANSFER
P. Belser et al., SUPRAMOLECULAR RU AND OR OS COMPLEXES OF TRIS(BIPYRIDINE) BRIDGING LIGANDS - SYNTHESES, ABSORPTION-SPECTRA, LUMINESCENCE PROPERTIES, ELECTROCHEMICAL-BEHAVIOR, INTERCOMPONENT ENERGY, AND ELECTRON-TRANSFER, Journal of the American Chemical Society, 115(10), 1993, pp. 4076-4086
The tris(bipyridine) tripod ligands bipyridyl-5-yl)carbonyl)benzylamin
o)methyl]benzene (1), dyl-5-ylcarbonyl)benzylamino)methyl)phenyl]benze
ne (2), and arbonyl)benzylamino)methyl)phenylyl)phenyl]benzene (3) hav
e been synthesized and their complexes 1[Ru(bpy)2]2+, 1[Ru(bpy)2]2(4+)
, 1[Ru(bpy)2]3(6+), 1[Os(bpy)2]3(6+), 1[Ru(bpy)2]2[Os(bpy)2]6+, 2[Ru(b
py)2]3(6+), 2[Os-bpy)2]3(6+), 2[Ru(bpy)2]2[Os(bpy)2]6+, and 3[Ru(bpy)2
]3(6+) have been prepared. All the complexes display very intense, lig
and centered absorption bands in the UV region and moderately intense
metal-to-ligand charge-transfer bands in the visible. Electrochemical
oxidation of each Ru(II) or Os(II) metal center occurs always at the s
ame potential (+1.30 V for Ru(II), +0.87 V for Os(II)), regardless of
tripod ligand and number and type of metal-based units that are presen
t in the supramolecular structure. The five homometallic Ru(II) specie
s exhibit the same luminescence properties, and this is also the case
for the two homometallic Os(II) species. The luminescence data obtaine
d for the two mixed-metal species show that electronic energy transfer
takes place from the Ru-based to the Os-based components. The efficie
ncy of energy transfer decreases in going from 1[Ru(bpy)2]2[Os(bpy)2]6
+ to 2[Ru(bpy)2]2[Os(bpy)2]6+, i.e., as the size of the spacer which l
inks the three arms of the bridging ligand increases. Oxidation of 1[R
u(bpy)2]3(6+), 2[Ru(bpy)2]3(6+), 1[Os(bpy)2]3(6+), and 2[Os(bpy)2]3(6) by Ce(IV) leads to mixed-valence species where the oxidized metal-ba
sed units quench the luminescent excited state of the units that are n
ot oxidized. The quenching efficiency decreases as the size of the spa
cer increases. The mechanisms of the quenching processes are discussed
. The results obtained indicate that at least in the case of the trinu
clear species of 2, there are conformers in which the quenching can ta
ke place very rapidly and conformers where it does not take place at a
ll.