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Title: Reductive quenching of the excited states of ruthenium(II) complexes containing 2,2[prime]-bipyridine, 2,2[prime]-bipyrazine, and 2,2[prime]-bipyrimidine ligands

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100096a015· OSTI ID:7079590
;  [1]
  1. Boston Univ., MA (United States)

The reductive quenching of the luminescent excited states of Ru(II) complexes of the general formula Ru-(bpy)[sub 3-m-z](bpm)[sub m](bpz)[sub z][sup 2+] (bpy = 2,2[prime]-bipyridine, bpm = 2,2[prime]-bipyrimidine, bpz = 2,2[prime]-bipyrazine, m and z = 0, 1,2,3 and m + z [le] 3) by aromatic amines and methoxybenzenes as nonsacrificial electron donors and by C[sub 2]O[sub 4][sup 2[minus]], EDTA, and TEOA as sacrificial donors in aqueous, acetonitrile, and propylene carbonate solution was examined by continuous and pulsed laser flash photolysis techniques. From k[sup q], a value of E[sup o] for the irreversible oxidation of TEOA ([minus]0.84 [+-] 0.12 V vs NHE) in acetonitrile was obtained. Values of the cage escape yield of redox products ([eta][sub cc]) showed weak or no dependencies on the driving forces of back electron transfer within the geminate redox pair in the solvent cage ([Delta]G[sub bt][degree]), suggesting that the simple model of competition between cage escape and back electron transfer may be inadequate to describe the results. A modification of the simple model, in which is introduced a kinetically important reorientation of the geminate redox pair, is proposed. 46 refs., 5 figs., 5 tabs.

OSTI ID:
7079590
Journal Information:
Journal of Physical Chemistry; (United States), Vol. 98:45; ISSN 0022-3654
Country of Publication:
United States
Language:
English