Department of Civil and Environmental Engineering, Louisiana State University, 3255 Patrick Taylor Hall, Baton Rouge, Louisiana 70803, United States.
Utah Water Research Laboratory, Department of Civil and Environmental Engineering, Utah State University, 4110 Old Main Hill, Logan Utah 84322-4110, United States.
ACS Nano. 2022 May 24;16(5):8309-8317. doi: 10.1021/acsnano.2c02281. Epub 2022 May 9.
Fullerene's low water solubility was a serious challenge to researchers aiming to harness their excellent photochemical properties for aqueous applications. Cationic functionalization of the fullerene cage provided the most effective approach to increase water solubility, but common synthesis practices inadvertently complicated the photochemistry of these systems by introducing iodide as a counterion. This problem was overlooked until recent work noted a potentiation effect which occurred when photosensitizers were used to inactivate microorganisms with added potassium iodide. In this work, several photochemical pathways were explored to determine the extent and underlying mechanisms of iodide's interference in the photosensitization of singlet oxygen by cationic fulleropyrrolidinium ions and rose bengal. Triplet excited state sensitizer lifetimes were measured via laser flash photolysis to probe the role of I in triplet sensitizer quenching. Singlet oxygen production rates were compared across sensitizers in the presence or absence of I, SO, and other anions. 3,5-Dimethyl-1-pyrazole was employed as a chemical probe for iodine radical species, such as I·, but none were observed in the photochemical systems. Molecular iodine and triiodide, however, were found in significant quantities when photosensitizers were irradiated in the presence of I and O. The formation of I in these photochemical systems calls into question the interpretations of prior studies that used I as a counterion for photosensitizer materials. As an example, MS2 bacteriophages were inactivated here by cationic fullerenes with and without I present, showing that I moderately accelerated the MS2 deactivation, likely by producing I. Production of I did not appear to be directly correlated with estimates of O concentration, suggesting that the relevant photochemical pathways are more complex than direct reactions between O and I in the bulk solution. On the basis of the results here, iodine photochemistry may be underappreciated and misunderstood in other environmental systems.
富勒烯的低水溶性是研究人员在将其优异的光化学性质应用于水相时面临的一个严重挑战。富勒烯笼的阳离子官能化提供了提高水溶性的最有效方法,但常见的合成方法通过引入碘化物作为抗衡离子,无意中使这些体系的光化学复杂化。直到最近的工作注意到一种增效作用,即在使用光敏剂灭活添加碘化钾的微生物时会发生这种作用,这个问题才被忽视。在这项工作中,探索了几种光化学途径,以确定碘化物在阳离子富勒烯吡咯啉离子和玫瑰红孟加拉敏化单线态氧的光化学中的干扰程度和潜在机制。通过激光闪光光解测量三重态激发态敏化剂的寿命,以探测 I 在三重态敏化剂猝灭中的作用。在存在或不存在 I、SO 和其他阴离子的情况下,比较了敏化剂的单线态氧产生速率。3,5-二甲基-1-吡唑被用作碘自由基物种(如 I·)的化学探针,但在光化学体系中未观察到。然而,当在存在 I 和 O 的情况下照射光敏剂时,发现了大量的分子碘和三碘化物。在这些光化学体系中形成 I 使得先前使用 I 作为光敏剂材料的抗衡离子的研究的解释受到质疑。例如,这里用带和不带 I 的阳离子富勒烯使 MS2 噬菌体失活,表明 I 适度加速了 MS2 的失活,可能是通过产生 I 来实现的。I 的产生似乎与 O 浓度的估计没有直接相关性,这表明相关的光化学途径比在体相溶液中 O 和 I 之间的直接反应更为复杂。基于这里的结果,碘光化学在其他环境系统中可能被低估和误解。