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   <subfield code="a">Uranyl-catalyzed chemiluminescent reaction of U4+ oxidation by dioxygen in aqueous HClO4 solution</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[S. Lotnik, L. Khamidullina, V. Kazakov]</subfield>
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   <subfield code="a">Chemiluminescence (CL) accompanying the reaction of U4+ with O2 in 0.0004-0.1M HClO4 was studied. It was found that the electron-excited uranyl ion (UO2 2+)* is the CL emitter. The fact that the reaction rate and the CL yield increase as the solution acidity decreases was explained by different reactivities of the U aq 4+ aquation and the products of its stepwise hydrolysis, UOH3+ and U(OH)2 2+, toward O2. Based on the results of analysis of the chain-radical mechanism of the reaction between U4+ and O2, it was concluded that transfer of an electron from the UO2 + ion to the oxidizing agent (a ·OH radical) is the most plausible elementary step of the reaction of (UO2 2+)* formation. It was found that the reaction rate, as well as the CL yield, increase substantially in the presence of uranyl ion. Catalytic action of UO2 2+ was explained by the formation of a UO2 2+·UO2 + complex, which reduces the rate of the UO2 + disproportionation reaction (UO2 + is an intermediate of the reaction and is involved in chain propagation), and by regeneration of the active center, UO2 +, in the reaction of UO2 2+ with U4+.</subfield>
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   <subfield code="a">uranium(IV)</subfield>
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