Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/30474
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 18074/20272 (89%)
造访人次 : 4371594      在线人数 : 1043
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: 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
    显示于类别:[藥理學院] 2008第五屆海峽化學、生物及材料研討會

    文件中的档案:

    档案 描述 大小格式浏览次数
    A7.pdf376KbAdobe PDF274检视/开启


    在CNU IR中所有的数据项都受到原著作权保护.

    TAIR相关文章

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