Kinetic Evidence of Tautomerism of Thiourea Dioxide in Aqueous Acidic Solutions

被引:13
|
作者
Cseko, Gyoergy [1 ,2 ]
Hu, Ying [1 ]
Song, Yanan [1 ]
Kegl, Timea R. [3 ]
Gao, Qingyu [1 ]
Makarov, Sergei V. [4 ]
Horvath, Attila K. [2 ]
机构
[1] China Univ Min & Technol, Sch Chem Engn, Xuzhou 2221111, Jiangsu, Peoples R China
[2] Univ Pecs, Dept Inorgan Chem, H-7624 Pecs, Hungary
[3] Univ Pecs, Janos Szentagothai Res Ctr, H-7624 Pecs, Hungary
[4] State Univ Chem & Technol, Ivanovo 153000, Russia
基金
中国国家自然科学基金;
关键词
Tautomerism; Kinetics; Autocatalysis; Reactivity; Sulfur; OXYHALOGEN-SULFUR CHEMISTRY; CHLORINE DIOXIDE; CHEMICAL OSCILLATORS; HYDROGEN-PEROXIDE; SYSTEMATIC DESIGN; GRAPHENE OXIDE; OXIDATION; MECHANISM; REDUCTANT; SULFITE;
D O I
10.1002/ejic.201400059
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Indirect experimental evidence of the existence of a sluggish tautomerism of thiourea dioxide in acidic aqueous solution was discovered while studying its oxidation by chlorine dioxide. Thiourea dioxide slowly rearranges into aminoiminomethanesulfinic acid, but the reactivity of these two species towards chlorine dioxide marginally differs. It was clearly demonstrated that thiourea dioxide reacts with chlorine dioxide in a relatively slow reaction in an autocatalytic fashion with respect to the carbon(IV) species. In contrast, reaction of aminoiminomethanesulfinic acid with chlorine dioxide is orders of magnitude faster but proceeds through a normal second-order process.
引用
收藏
页码:1875 / 1879
页数:5
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