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Oxide radical ion
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Mezyk, S.P.; Elliot, A.J.
J. Chem. Soc., Faraday Trans. 90, 831-836 (1994)
Reaction: O·- + IO3- ®
IO42-
Solvent: H2O
k = 1.8 × 109(L mol-1 s-1), pH = 14
Experimental method: Pulse radiolysis
Analytical method: vis-UV absorption
Data type: Absolute value measured directly
Product buildup kinetics at 360 nm in N2O-satd. soln. contg. (1-10) × 10-4 mol L-1 iodate.
Tendler, Y.; Faraggi, M.
J. Chem. Phys. 58, 848-853 (1973)
Reaction: O·- + IO3- ®
IO3 + OH-
Solvent: H2O
k = 1.6 × 109(L mol-1 s-1), pH = 12.0
Experimental method: Pulse radiolysis
Analytical method: vis-UV absorption
Data type: Absolute value measured directly
Product buildup kinetics at 360 nm (IO3)2·-.
Barat, F.; Gilles, L.; Hickel, B.; Lesigne, B.
J. Phys. Chem. 76, 302-307 (1972)
Reaction: O·- + IO3- ®
IO3 + OH-
Solvent: H2O
k = 3 × 109(L mol-1 s-1), pH = 12.6
Experimental method: Pulse radiolysis
Analytical method: vis-UV absorption
Data type: Absolute value measured directly
Product buildup kinetics at 360 nm; cor. for ·OH reaction.
Amichai, O.; Treinin, A.
J. Phys. Chem. 74, 830-835 (1970)
Reaction: O·- + IO3- ®
IO3 + OH-
Reference Reaction: O·- + O2 ®
Solvent: H2O
pH range 12.4 to 13.6
k = 1.3 × 109(L mol-1 s-1), kreference = 3.6 × 109(L mol-1 s-1)
Experimental method: Flash photolysis
Analytical method: chemical analysis
Data type: Relative value measured directly
Competition kinetics