College of Food and Biological Engineering, Jimei University, Xiamen, 361021, PR China.
Key Laboratory of Bioorganic Phosphorous Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing, 100084, PR China.
Phytochemistry. 2021 Oct;190:112853. doi: 10.1016/j.phytochem.2021.112853. Epub 2021 Jun 30.
A series of naturally occurring 3',4'-dihydroxy aurones have been studied with regard to multiple free radical scavenging reactions in the gas and two liquid phases using density functional theory (DFT). All of the aurones prefer to perform (2 + n)-HAT mechanism to trap 2 + n free radicals, where n is the sum of the numbers of catechol and guaiacyl units in the gas and benzene phases. The second HAT reaction favours occurring in the same catechol moiety of the first HAT mechanism occurring OH group due to the formation of a stable quinone and the highly exothermic step of the final stable product formation. The catechol and guaiacyl moieties show increased potency for the second and fourth H/e reactions. In the water phase, aurones can perform multiple H/e reactions through nPL-ET-nHAT-(n+1-n)ET mechanism, where n is the number of OH groups and n is the number of guaiacyl moieties.
一系列天然存在的 3',4'-二羟基苯并吡喃酮已被研究,以了解其在气相和两种液相中通过密度泛函理论(DFT)进行的多种自由基清除反应。所有的苯并吡喃酮都倾向于通过(2 + n)-HAT 机制来捕获 2 + n 自由基,其中 n 是气相和苯相中山柰酚和愈创木酚单元数的总和。由于形成稳定的醌和最终稳定产物形成的高度放热步骤,第二个 HAT 反应有利于在第一个 HAT 机制发生 OH 基团的同一儿茶酚部分发生。儿茶酚和愈创木酚部分对第二个和第四个 H/e 反应表现出更强的活性。在水相,苯并吡喃酮可以通过 nPL-ET-nHAT-(n+1-n)ET 机制进行多次 H/e 反应,其中 n 是 OH 基团的数量,n 是愈创木酚部分的数量。