The temperature dependence of the emission lifetime of the series of complexes Ru(bpy),(4,4'-dpb): ? (bpy = 2,2'-bipyridine, 4,4'-dpb = 4,4'-diphenyL2,2'-bipyridine) has been studied in propionitrile/butyronitrile (4:5 u/u) solutions in the range 90-293 K. The obtained photophysical parameters show
Synthesis and Photophysical Properties of New 2,2′-Bipyridine-Bridged Bis[ruthenium(II)tris-2,2′-bipyridine] Complexes
✍ Scribed by König, Burkhard ;Zieg, Harald ;Cola, Luisa De ;Balzani, Vincenzo ;Nimtz, Manfred ;Balzani, Vincenzo
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1997
- Tongue
- English
- Weight
- 500 KB
- Volume
- 130
- Category
- Article
- ISSN
- 0009-2940
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✦ Synopsis
We have synthesized a new type of tris-2,2'-bipyridine ligand of 7 and 8 do not interact appreciably, as is evident from their with 4,4'-and 6,6'-disubstituted 2,2'-bipyridine (bpy) units. electrochemical and photophysical data. The lifetime of the The terminal 4,4'-disubstituted 2,2'-bipyridine moieties are excited state of compound 7 at 77 K is similar to that of selectively coordinated by Ru( bpy) (bpy = 2,2 'bipyridine) , Ru (bpy) ,(4,4 ' -dimethyl-2,2 ' -bip yridine) , whereas that of whereas the central 2,2'-bipyridine ligand does not partici-compound 8 under the same conditions is comparatively pate in any metdl ion coordination. The two Ru(bpy), units long.
Multimetallic assemblies of defined structure are key design targets for the study of energy-and electron transfer [']. Ruthenium complexes of polypyridinc ligands play a central properties, and favorable photophysical characteristicsr21. Most di-and oligonuclear ruthenium complexes have been synthesized by metal complexation of a multitopic ligandIsl. This procedure does not always provide full control over the final composition of the oligonuclear ~ornplex[~J. The selective synthesis of assemblies with free binding sites is especially ditficult. We report here on the preparation of new tris-2,2'-bipyridine ligands with different binding sites and their selective twofold coordination by R ~( b p y ) ~ [ ~] moieties. The redox, absorption, and luminescence properties of the 2,2'-bipyridine-bridged bis(ruthenium) complexes thus obtained have been investigated.
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## Abstract The existence of two independent chromophores in [Ru(bipy)~2~(H~2~V)]^+^, where H~2~V^−^ = violurate anion and bipy = 2,2′bipyridine, was demonstrated by comparing its resonance Raman spectra with those displayed by the [Ru(H~2~V)~3~]^−^ analogue. In the former, the electronic band at 4
The electrode processes of tris(2,2'-bipyridine)iron(II) and tris(2,2'-bipyridine)iron(III) complexes at the rotated platinum electrode and the dropping mercury electrode (dme) in acetonitrile solutions have been investigated by the measurement of current/potential curves, dc and ac polarograms and