The pulse radiolysis of aqueous solutions of simple RCN compounds

I.G. Draganić, Z.D. Draganić, V.M. Marković
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引用次数: 19

Abstract

Fast kinetic spectrophotometry was used to study the absorption spectra of short-living intermediates produced by reactions of RCN molecules with H, eaq and OH. The spectra were obtained on the microsecond time scale after an electron pulse from a Febetron 707 accelerator in aqueous solutions of the following compounds: hydrocyanic acid, acetonitrile, propionitrile, malononitrile and succinonitrile. It has been found that all intermediates absorb in the U.V. range (λ⩽300 nm) and disappear by fast bimolecular processes with decay rate constants of about 109dm3mol−1s−1. In the presence of an efficient scavenger for hydroxyl radicals, the same transient spectra were registered in acid and neutral solutions suggesting that the protonations of eaq adducts of these RCN molecules were complete within a submicrosecond time interval.

简单RCN化合物水溶液的脉冲辐射分解
采用快速动力学分光光度法研究了RCN分子与H、eaq−和OH反应产生的短寿命中间体的吸收光谱。用Febetron 707加速器在氢氰酸、乙腈、丙腈、丙二腈和丁二腈的水溶液中施加电子脉冲后,在微秒时间尺度上获得了光谱。结果表明,所有中间体均在uv波段(λ≤300 nm)吸收,并以快速的双分子过程消失,衰变速率常数约为109dm3mol−1s−1。在羟基自由基的有效清除剂的存在下,在酸性和中性溶液中记录了相同的瞬态光谱,这表明这些RCN分子的eaq -加合物的质子化在亚微秒的时间间隔内完成。
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