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Benzothiazoline Converts SO2 to Sulfuric Acid en Route to Benzothiazole

机译:苯并噻唑啉在将二氧化硫转化为硫酸的过程中转化为苯并噻唑

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By a new sustainable strategy, sulfur dioxide (SO2) was converted at room temperature into sulfuric acid by taking advantage of the spontaneous aerial oxidation of benzothiazoline into benzothiazole. 2-(4- Methoxyphenyl)benzothiazoline (HL) was reacted with SO2 at room temperature, and the adduct upon reaction with aerial oxygen produced 2- (4-methoxyphenyl)benzothiazolium bisulfate. The same strategy was applied on [CdL2] and [ZnL2] and found to work better than neat benzothiazoline. Bunte salt, S-(2-((pyridin-1-ium-2-ylmethyl)amino)phenyl) thiosulfate, was obtained upon reacting SO2 with 2-(pyridin-2-yl)-2,3-dihydrobenzothiazole which is an important clue for the intermediates involved in the S-oxygenation of SO2 bound on electron rich centers. This sustainable route offers a new avenue of utilizing the suicidal reaction of benzothiazoline into benzothiazole in the activation of SO2 with the help of aerial oxygen.
机译:通过一种新的可持续发展战略,利用苯并噻唑啉的自发空中氧化作用,将二氧化硫(SO2)在室温下转化为硫酸。使2-(4-甲氧基苯基)苯并噻唑啉(HL)在室温下与SO 2反应,并且该加合物在与空气氧反应时产生硫酸氢2-(4-甲氧基苯基)苯并噻唑鎓。将相同的策略应用于[CdL2]和[ZnL2],发现其效果优于纯苯并噻唑啉。使SO2与2-(吡啶-2-基)-2,3-二氢苯并噻唑反应,制得戊酸酯盐S-(2-((吡啶-1-基-2-基甲基)氨基)苯基)硫代硫酸盐。富电子中心上SO2的S-加氧反应所涉及的中间体的重要线索。这种可持续的途径提供了一条新途径,可以利用苯并噻唑啉的自杀反应转化为苯并噻唑,借助空气中的氧气活化SO2。

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