Department of Chemistry, Aarhus University, Aarhus, Denmark.
Photochem Photobiol. 2019 Jan;95(1):202-210. doi: 10.1111/php.12971. Epub 2018 Aug 1.
Uric acid and/or its monoanion has long been used as chemical-trapping agents to demonstrate the presence of singlet oxygen, O (a Δ ), in aqueous systems. "Oxidative bleaching" of uric acid, generally monitored through changes in the uric acid absorption spectrum, is often used in support of claims for the intermediacy of O (a Δ ). The bleaching of uric acid has also been used to quantify photosensitized O (a Δ ) yields in selected systems. Unfortunately, experiments performed to these ends often neglect processes and phenomena that can influence the results obtained. For the present study, we experimentally examined the behavior of uric acid under a variety of conditions relevant to the photoinitiated creation and subsequent removal of O (a Δ ). Although the oxidative destruction of uric acid can indeed be a useful tool in some cases, we conclude that caution must be exercised such as not to incorrectly interpret the data obtained.
尿酸及其一阴离子长期以来一直被用作化学捕获剂,以证明单线态氧 O(aΔ)在水相体系中的存在。尿酸的“氧化漂白”通常通过尿酸吸收光谱的变化来监测,这通常被用于支持 O(aΔ)中间体的说法。尿酸的漂白也被用于定量选定体系中光致产生的 O(aΔ)的产率。不幸的是,为了达到这些目的而进行的实验往往忽略了可能影响所得到结果的过程和现象。在本研究中,我们根据与光引发的 O(aΔ)的生成和随后的去除相关的各种条件,实验性地研究了尿酸的行为。虽然尿酸的氧化破坏在某些情况下确实是一个有用的工具,但我们得出结论,必须谨慎行事,以免错误地解释所得到的数据。