首页> 外文期刊>Journal of the Chemical Society. Perkin Transactions 2 >Reaction of OH radicals with benzoquinone in aqueous solutions. A pulse radiolysis study
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Reaction of OH radicals with benzoquinone in aqueous solutions. A pulse radiolysis study

机译:OH自由基与苯醌在水溶液中的反应。脉冲放射分解研究

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Hydroxyl radicals have been generated by pulse radiolysis in N2O-saturated aqueous solutions, Their addition to 1,4-benzoquinone BQ (k(3) = 6.6 x 10(9) dm(3) mol(-1) s(-1) by competition with thiocyanate) in neutral solution leads to a build-up of optical absorption that shows different rates at wavelengths at around 330 and at >400 nm, At 330 nm the rate of build-up is proportional to the benzoquinone concentration, and its rate constant agrees with the value (k(3)) obtained by competition. At the longer wavelengths, it becomes independent of benzoquinone concentration beyond 4 x 10(-4) mol dm(-3) (k(6) = 6.9 x 10(5) s(-1)). Kinetic analysis in the ns time-range show that the primarily-generated benzoquinone-OH-adduct radical 1 undergoes rapid (k(4) = 2.5 x 10(6) s(-1)) keto-enol tautomerization yielding the 2,4-dihydroxyphenoxyl radical 2, To gain support for this proposed reaction, radical 2 [pK(a)(2) approximate to 4.9 +/- 0.2] has been independently generated by one-electron oxidation of 1,2,4-trihydroxybenzene using (OH)-O-. in acidic or N-3(.) in neutral and basic solution. Its absorption characteristics compare favourably with those observed in the benzoquinone system. On the basis of spectrophotometric and conductometric data it is proposed that in neutral solution the radical anion 2a is rapidly oxidized by benzoquinone itself (k(15) greater than or equal to 2 x 10(9) dm(3) mol(-1)) into the end product 2-hydroxy-1,4-benzoquinone anion 4a [pK(a)(3) = 4.1 +/- 0.1; lambda(max)(4) = 380 nm; lambda(max)(4a) = 482 nm] and the semibenzoquinone radical anion 3a, The latter decays bimolecularly into benzoquinone and hydroquinone (2k(16) = 3.1 x 10(18) dm(3) mol(-1) s(-1)). In acidic solution the rate of oxidation of 2 by benzoquinone is considerably slower (k(13) less than or equal to 2.4 x 10(7) dm(3) mol(-1) s(-1)). The assignment of the final product to 2-hydroxy-1,4-benzoquinone 4 has been confirmed by the absorption characteristics and pK(a) value of the authentic material obtained by the two-electron electrochemical oxidation of 1,2,4-trihydroxybenzene. [References: 19]
机译:在N2O饱和水溶液中通过脉冲辐射分解产生了羟基自由基,它们添加到1,4-苯醌BQ(k(3)= 6.6 x 10(9)dm(3)mol(-1)s(-1)通过与硫氰酸盐竞争)在中性溶液中导致光吸收的累积,该吸收在波长约330和> 400 nm处显示出不同的速率。在330 nm处,该累积速率与苯醌浓度成正比,速率常数与通过竞争获得的值(k(3))一致。在更长的波长处,它变得与苯醌浓度无关,超过4 x 10(-4)mol dm(-3)(k(6)= 6.9 x 10(5)s(-1))。在ns时间范围内的动力学分析表明,初生的苯醌-OH加合物自由基1迅速发生(k(4)= 2.5 x 10(6)s(-1))酮-烯醇互变异构,生成2,4 -二羟基苯氧基基团2,为了获得对该拟议反应的支持,基团2 [pK(a)(2)约为4.9 +/- 0.2]是通过使用()进行1,2,4-三羟基苯的单电子氧化而独立生成的OH)-O-。在酸性或N-3(。)中和碱性溶液中。它的吸收特性与在苯醌体系中观察到的吸收特性相比具有优势。根据分光光度法和电导数据,建议在中性溶液中自由基阴离子2a被苯醌本身快速氧化(k(15)大于或等于2 x 10(9)dm(3)mol(-1) )生成最终产物2-羟基-1,4-苯醌阴离子4a [pK(a)(3)= 4.1 +/- 0.1; lambda(max)(4)= 380纳米; lambda(max)(4a)= 482 nm]和半苯醌醌阴离子3a,后者双分子衰减成苯醌和对苯二酚(2k(16)= 3.1 x 10(18)dm(3)mol(-1)s(- 1))。在酸性溶液中,苯醌对2的氧化速度要慢得多(k(13)小于或等于2.4 x 10(7)dm(3)mol(-1)s(-1))。通过1,2,4-三羟基苯的双电子电化学氧化获得的真实材料的吸收特性和pK(a)值已确认最终产物为2-羟基-1,4-苯醌4 。 [参考:19]

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