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实时观察水溶液中碳酸的形成。

Real-time observation of carbonic acid formation in aqueous solution.

机构信息

Max Born Institut für Nichtlineare Optik und Kurzzeitspektroskopie, Max Born Strasse 2A, D-12489 Berlin, Germany.

出版信息

Science. 2009 Dec 18;326(5960):1690-4. doi: 10.1126/science.1180060. Epub 2009 Nov 12.

Abstract

Despite the widespread importance of aqueous bicarbonate chemistry, its conjugate acid, carbonic acid, has remained uncharacterized in solution. Here we report the generation of deuterated carbonic acid in deuterium oxide solution by ultrafast protonation of bicarbonate and its persistence for nanoseconds. We follow the reaction dynamics upon photoexcitation of a photoacid by monitoring infrared-active marker modes with femtosecond time resolution. By fitting a kinetic model to the experimental data, we directly obtain the on-contact proton-transfer rate to bicarbonate, previously inaccessible with the use of indirect methods. A Marcus free-energy correlation supports an associated pKa (Ka is the acid dissociation constant) of 3.45 +/- 0.15, which is substantially lower than the value of 6.35 that is commonly assumed on the basis of the overall carbon dioxide-to-bicarbonate equilibrium. This result should spur further exploration of acid-base reactivity in carbon dioxide-rich aqueous environments such as those anticipated under sequestration schemes.

摘要

尽管水合碳酸氢盐化学具有广泛的重要性,但它的共轭酸——碳酸——在溶液中仍未被描述。在这里,我们报告了通过超快质子化碳酸氢盐在重水溶液中生成氘代碳酸,其在纳秒时间内稳定存在。我们通过监测飞秒时间分辨率的红外活性标记模式来跟踪光酸光解后的反应动力学。通过将动力学模型拟合到实验数据中,我们直接获得了之前无法通过间接方法获得的与碳酸氢盐的接触质子转移速率。马库斯自由能相关支持相关的 pKa(pKa 是酸离解常数)为 3.45 +/- 0.15,这明显低于通常根据二氧化碳到碳酸氢盐的整体平衡假设的 6.35 值。这一结果应该会进一步激发对富含二氧化碳的水相环境中的酸碱反应性的探索,例如封存方案中预期的环境。

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