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By Richard C. Alkire, Charles W. Tobias

ISBN-10: 352729385X

ISBN-13: 9783527293858

This sequence, previously edited by means of Heinz Gerischer and Charls V. Tobias, now edited by way of Richard C. Alkire and Dieter M. Kolb, has been warmly welcomed via scientists world-wide that is mirrored within the studies of the former volumes: 'This is a necessary booklet for researchers in electrochemistry; it covers components of either primary and functional significance, with studies of top of the range. the fabric is particularly good awarded and the alternative of issues displays a balanced editorial coverage that's welcomed.' The Analyst

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Extra resources for Advances in electrochemical science and engineering

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66) may be further simplified: + + Appropriate values of these rates are not directly available, but a quantitative estimate is possible in view of the experimental values of ECL efficiencies that have 38 " ' - 0 A. Kapturkiewicz I 1 2 3 4 5 6 Fig. 18. Values of the km/k3 ratio (evaluated from the experimental efficiencies of formation of the excited state) as a function of the solvent longitudinal relaxation time TL. Data for 4-(9-anthryl)-N,N,3,5-tetramethylaniline in acetonitrile (ACN), propionitrile (PN), butyronitrile (BN), propylene carbonate (PC), sulfolane (TMS) and y-butyrolactone (BL) solutions.

36, which is in agreement with the value of 1/3 expected for the case of a fully dissociative triplet-triplet encounter pair. 74 CPat 293 K) their larger PF values suggest that in this particular case the triplet-triplet upconversion has already take place at room temperature. Resuming, the statistical factors evaluated as described above depend on temperature, changing from near unity (at low temperatures) to 1/3 (at room temperature); this indicates that the T dependence of q5ecl may be described in the terms of Eq.

The electron transfer reaction is still extremely rapid, but much less energy needs to be dissipated. The formation of the excited singlet is the least (if at all) exergonic and much less thermodynamically favored. The preference for the given reaction pathway is related to the free-energy difference between the oxidized and reduced precursors. The formation of the excited product requires this difference to be equal to or higher than the energy difference between the excited and ground electronic states.

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Advances in electrochemical science and engineering by Richard C. Alkire, Charles W. Tobias


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