A density functional theory study for the role of end groups on the antioxidative potency of carotenoids

Fu Xing Liao, Ching-Han Hu

研究成果: Article

3 引文 斯高帕斯(Scopus)

摘要

Role of carotenoid end groups on their chainbreaking potency against lipid peroxidation was explored using density functional theory. Hydrogen abstraction and addition of the peroxide and O2 of the resultant radicals were investigated. The protective potency of CARs is exhibited by their faster reactions with the peroxide radical than fatty acid, and by the much reduced reactivity of the initiated radical toward O2. 3,3'-Dihydroxyisorenieratene (DHIR), which consists of hydroxyaryl (3-hydroxy-φ) end groups, is by far the most efficient chain-breaking antioxidant. The quinone form of DHIR is also an effective antioxidant. 4-Oxo functional group in β-ring enhances the antioxidative potency of carotenoids, while 3-hydroxyl functional group in β-ring does not have a noticeable effect.

原文English
頁(從 - 到)1-13
頁數13
期刊Theoretical Chemistry Accounts
132
發行號5
DOIs
出版狀態Published - 2013 三月 22

    指紋

All Science Journal Classification (ASJC) codes

  • Physical and Theoretical Chemistry

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