碳酸
碳酸氢盐
二氧化碳
化学
水溶液
碳酸酐酶
无机化学
动力学
红外光谱学
有机化学
量子力学
物理
酶
作者
Katrin Adamczyk,Mirabelle Prémont‐Schwarz,Dina Pines,Ehud Pines,Erik T. J. Nibbering
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2009-12-18
卷期号:326 (5960): 1690-1694
被引量:266
标识
DOI:10.1126/science.1180060
摘要
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.
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