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水微滴中紫精化合物的自发还原诱导降解及其主客体络合抑制作用

Spontaneous Reduction-Induced Degradation of Viologen Compounds in Water Microdroplets and Its Inhibition by Host-Guest Complexation.

作者信息

Gong Chu, Li Danyang, Li Xilai, Zhang Dongmei, Xing Dong, Zhao Lingling, Yuan Xu, Zhang Xinxing

机构信息

College of Chemistry, Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Renewable Energy Conversion and Storage Center (ReCAST), Haihe Laboratory of Sustainable Chemical Transformations, Beijing National Laboratory for Molecular Sciences, Frontiers Science Center for New Organic Matter, Shenzhen Research Institute, Nankai University, Tianjin 300071, China.

出版信息

J Am Chem Soc. 2022 Mar 2;144(8):3510-3516. doi: 10.1021/jacs.1c12028. Epub 2022 Feb 15.

Abstract

Water serves as an inert environment for the dispersion and application of many kinds of herbicides. Viologen compounds, a type of widely used but highly toxic herbicide, are stable in bulk water, whose half-life can be up to 23 weeks in natural water, imposing a severe health risk to mammals. In this study, we present the striking results of the spontaneous and ultrafast reduction-induced degradation of three viologen compounds in water microdroplets and provide the concentration, time, temperature dependence, mechanism, and scale-up of the reactions. We postulate that the electrons existing at the air-water interface of the microdroplets due to the unique redox potential therein initiate the reduction, from which further degradation occurs. The host-guest complexation between cucurbit[7]uril and viologens only slightly changes the redox potential of viologens in the bulk but completely inhibits the reactions in microdroplets, adding to the uniqueness of the redox potentials at the air-water interfaces of microdroplets. Taken together, microdroplets might have been functioning as naturally occurring ubiquitous tiny electrochemical cells for a plethora of unique redox reactions that were thought to be impossible in the bulk water.

摘要

水为多种除草剂的分散和应用提供了一个惰性环境。紫精化合物是一种广泛使用但毒性很高的除草剂,在大量水中很稳定,其在天然水中的半衰期可达23周,对哺乳动物构成严重的健康风险。在本研究中,我们展示了三种紫精化合物在微滴水中自发且超快还原诱导降解的惊人结果,并给出了反应的浓度、时间、温度依赖性、机理及放大情况。我们推测,由于微滴气-水界面处独特的氧化还原电位而存在的电子引发了还原反应,进而发生进一步降解。葫芦[7]脲与紫精之间的主客体络合仅略微改变了大量紫精的氧化还原电位,但完全抑制了微滴中的反应,这进一步凸显了微滴气-水界面氧化还原电位的独特性。综上所述,微滴可能一直充当着自然存在的无处不在的微小电化学电池,用于进行大量在大量水中被认为不可能发生的独特氧化还原反应。

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