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Photoinduced electron transfer within ion pairs. Direct measure of the intramolecular electron-transfer quenching constant
Affiliation:1. Department of Chemistry, Texas A&M University, College Station, TX 77843, USA;5. Sri Venkateswara College, Department of Chemistry, University of Delhi, New Delhi, India;6. Kalindi College, Department of Chemistry, University of Delhi, New Delhi, India
Abstract:The electron-transfer quenching of the luminescence emission of Ru(bpy)32+ (bpy = 2,2′-bipyridine) by CoSiW11O39H2O6− has been studied by steady-state and pulsed techniques. Both static and dynamic quenching were observed. The luminescence emission was found to decrease with time according to two distinct exponential decays. A kinetic analysis of the system shows that the faster decay corresponds to the intramolecular electron transfer rate constant within the =Ru(bpy)32+ -polytungstate ion pair and that the slower decay is related to the dynamic quenching.
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