We report the synthesis of six new dendrimers built around a [Ru(bpy)3]2+-type core (bpy = 2,2'-bipyridine) and bearing up to 24 4'- tert-butylphenyloxy or 48 benzyl units in the periphery. The metallodendrimers were obtained by complexation of ruthenium trichloride or Ru(bpy)2Cl2 with bipyridine ligands carrying dendritic wedges in the 4,4'- positions. The absorption spectra and luminescence properties (spectra and lifetimes at 77 and 298 K; quantum yields at 298 K) of the six novel compounds are reported. All of them show the characteristic luminescence of the [Ru(bpy)3]2+-type core unit. The dendritic branches protect the luminescent excited state of the core by dioxygen quenching. For the three compounds containing the 4'-tert-butylphenyloxy peripheral units, the electrochemical behavior and the excited-state quenching via electron transfer were also studied. The electrochemical experiments have evidenced an oxidation and three reduction one-electron processes centered in the [Ru(bpy)3]2+-type core and two multielectron oxidation processes involving the dioxybenzene- and oxybenzene-type units of the dendritic branches. The core of the largest dendrimer shows an electrochemical behavior typical of encapsulated electroactive units. The reaction of the luminescent excited state of the [Ru(bpy)3]2+-type core with three electron-transfer quenchers (namely, methyl viologen dication, tetrathiafulvalene, and anthraquinone- 2,6-disulfonate anion) was found to take place by a dynamic mechanism in all cases. The quenching rate constants, obtained by Stern-Volmer kinetic analysis, are compared with those found for the simple [Ru(bpy)3]2+ complex. The results show that, for each quencher, the value of the rate constant decreases with increasing number and size of the dendritic branches. For the second-generation dendrimer containing 24 4'-tert-butylphenyloxy units at the periphery, the rate constant of the reaction with methyl viologen is more than 1 order of magnitude smaller than that of the 'naked' [Ru(bpy)3]2+ complex. All the experiments were performed in acetonitrile solution, except for luminescence experiments at 77 K where butyronitrile was used.
Vogtle, F., Plevoets, M., Nieger, M., Azzellini, G.C., Credi, A., De Cola, L., et al. (1999). Dendrimers with a photoactive and redox-active [Ru(bpy)3]2+-type core: Photophysical properties, electrochemical behavior, and excited-state electron-transfer reactions. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 121(26), 6290-6298 [10.1021/ja990430t].
Dendrimers with a photoactive and redox-active [Ru(bpy)3]2+-type core: Photophysical properties, electrochemical behavior, and excited-state electron-transfer reactions
Credi A.;De Cola L.;Venturi M.;Balzani V.
1999
Abstract
We report the synthesis of six new dendrimers built around a [Ru(bpy)3]2+-type core (bpy = 2,2'-bipyridine) and bearing up to 24 4'- tert-butylphenyloxy or 48 benzyl units in the periphery. The metallodendrimers were obtained by complexation of ruthenium trichloride or Ru(bpy)2Cl2 with bipyridine ligands carrying dendritic wedges in the 4,4'- positions. The absorption spectra and luminescence properties (spectra and lifetimes at 77 and 298 K; quantum yields at 298 K) of the six novel compounds are reported. All of them show the characteristic luminescence of the [Ru(bpy)3]2+-type core unit. The dendritic branches protect the luminescent excited state of the core by dioxygen quenching. For the three compounds containing the 4'-tert-butylphenyloxy peripheral units, the electrochemical behavior and the excited-state quenching via electron transfer were also studied. The electrochemical experiments have evidenced an oxidation and three reduction one-electron processes centered in the [Ru(bpy)3]2+-type core and two multielectron oxidation processes involving the dioxybenzene- and oxybenzene-type units of the dendritic branches. The core of the largest dendrimer shows an electrochemical behavior typical of encapsulated electroactive units. The reaction of the luminescent excited state of the [Ru(bpy)3]2+-type core with three electron-transfer quenchers (namely, methyl viologen dication, tetrathiafulvalene, and anthraquinone- 2,6-disulfonate anion) was found to take place by a dynamic mechanism in all cases. The quenching rate constants, obtained by Stern-Volmer kinetic analysis, are compared with those found for the simple [Ru(bpy)3]2+ complex. The results show that, for each quencher, the value of the rate constant decreases with increasing number and size of the dendritic branches. For the second-generation dendrimer containing 24 4'-tert-butylphenyloxy units at the periphery, the rate constant of the reaction with methyl viologen is more than 1 order of magnitude smaller than that of the 'naked' [Ru(bpy)3]2+ complex. All the experiments were performed in acetonitrile solution, except for luminescence experiments at 77 K where butyronitrile was used.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
