English  |  正體中文  |  简体中文  |  Items with full text/Total items : 18270/20497 (89%)
Visitors : 11757789      Online Users : 839
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/30474


    標題: Oxidation of Flavonoids by Pentaammineruthium (III) complexes
    作者: Jay Sung (宋杰)
    Kaisheng Huang (黃凱聲)
    Andrew Yeh (葉玉堂)
    貢獻者: Department of Chemistry, Tunghai Univerity
    日期: 2008-07
    上傳時間: 2017-12-04 15:52:02 (UTC+8)
    摘要: Kinetic study of the oxidation of catechin and rutin, subclass of flavonoids mainly found in teas and red wine, by Ru(NH3)5L3+(L=pzCH3+,pz, isn) complexes were carried out over a pH range 0-7.6.The rate law of the reaction involves a rate determining step of one electron oxidation of the flavonoids in the form of H2X (k0), HX- (k1) and X2- (k2) by Ru(NH3)5L3+ complexes to from the cooresponding radicals, following the rapid scavenge of radicals by Ru(lll) complexes. The rate constants of oxidation in different forms of flavonoids were summarized in Table 1. With the measured k0, k1 and k2, the self-exchange rate constants (kex) can be calculated on the basis of Marcus theory, and the results are listed in Table 2. The comparison of kex of flavonoids with that of the catechol and the ascorbic acid suggest that active sites of flavonoids with that of the catechol and the ascorbic acid suggest that the active sites of oxidation go to the catechol ring of the flavonoids and the antioxidative reactivity of flavonoids is greater than that of the ascorbic acid by at least 3 orders of magnitude.
    關聯: 第五屆海峽化學、生物及材料研討會,起迄日:2008/07/21-2008/07/22,地點:嘉南藥理科技大學
    Appears in Collections:[藥理學院] 2008第五屆海峽化學、生物及材料研討會

    Files in This Item:

    File Description SizeFormat
    A7.pdf376KbAdobe PDF323View/Open


    All items in CNU IR are protected by copyright, with all rights reserved.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback