SUPRAMOLECULAR RU AND OR OS COMPLEXES OF TRIS(BIPYRIDINE) BRIDGING LIGANDS - SYNTHESES, ABSORPTION-SPECTRA, LUMINESCENCE PROPERTIES, ELECTROCHEMICAL-BEHAVIOR, INTERCOMPONENT ENERGY, AND ELECTRON-TRANSFER

Citation
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
Citations number
65
Categorie Soggetti
Chemistry
ISSN journal
00027863
Volume
115
Issue
10
Year of publication
1993
Pages
4076 - 4086
Database
ISI
SICI code
0002-7863(1993)115:10<4076:SRAOOC>2.0.ZU;2-8
Abstract
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.