English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 63246/95943 (66%)
造访人次 : 4822039      在线人数 : 131
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU 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://tkuir.lib.tku.edu.tw/dspace/handle/987654321/32692


    题名: 內雙羥雙加氧酶模型具兒茶酚酶活性之鐵(III)錯合物研究
    其它题名: Studies on intradiol dioxygenase model with catecholase activity of iron(III) complexes
    作者: 羅順益;Lo, Shun-i
    贡献者: 淡江大學化學學系碩士班
    魏和祥;Wei, Ho-hsiang
    关键词: 內雙羥雙加氧酶模型;鐵(III)錯合物;兒茶酚酶活性;X-ray結構;EPR光譜;Intradiol Dioxygenase Model;Iron(III) complexes;Catecholase Activity;X-ray structure;EPR spectrum
    日期: 2008
    上传时间: 2010-01-11 02:34:13 (UTC+8)
    摘要: 本論文合成一系列內雙羥雙加氧酶模型具兒茶酚酶活性之鐵(III)錯合物且性質由X-ray單晶繞射儀、UV-Vis光譜、元素分析儀及電化學方法來分析。

    酵素-受質型錯合物及配位基:
    (1) [Fe(L1)(C6Br4O2)]
    (2) [Fe(L2)(C6Cl4O2)]2
    (3) [Fe(L3)(C6Br4O2)(CH3OH)2]
    (4) [Fe(L4)(C6Br4O2)]
    (5) [Fe(L5)(C6Cl4O2)(CH3CN)]

    L1: 2-((E)-(2-(2-aminoethylamino)ethylimino)methyl)-4-chloro-phenol
    L2: 4-((E)-(2-(2-aminoethylamino)ethylimino)methyl)-benzene-1,3-diol
    L3: 2-((E)-(2-(2-aminoethylamino)ethylimino)methyl)-6-ethoxy-phenol
    L4: 2-((E)-(3-(3-aminopropylamino)propylimino)methyl)-4-bromo-phenol
    L5: 2-((E)-(3-(3-aminopropylamino)propylimino)methyl)-4,6-dibromo-phenol

    加入兒茶酚陰離子3,5-di-tert-butylcatechol(3,5-DTBC)與[Fe(L1~5)Cl2]反應,可藉由UV-Vis光譜測量,根據其吸收位置(λ=400nm)可發現有Diquinone的生成,表示內雙羥雙加氧酶模型的鐵(III)錯合物具有兒茶酚酶活性,且路易士酸性越強的錯合物具有較佳的兒茶酚酶催化反應性。從電化學的分析中,也能得到相同之結果。
    A seiries Intradiol Dioxygenase Model of iron(III) complexes as funtionl model compounds for Catecholase Activity were synthesized and characterized by X-ray single crystal diffraction, UV-Vis spectroscopy, element analyzer, and electronchemical analysises.

    Enzyme-substrate complexes and ligands:
    (1) [Fe(L1)(C6Br4O2)]
    (2) [Fe(L2)(C6Cl4O2)]2
    (3) [Fe(L3)(C6Br4O2)(CH3OH)2]
    (4) [Fe(L4)(C6Br4O2)]
    (5) [Fe(L5)(C6Cl4O2)(CH3CN)]

    L1: 2-((E)-(2-(2-aminoethylamino)ethylimino)methyl)-4-chloro-phenol
    L2: 4-((E)-(2-(2-aminoethylamino)ethylimino)methyl)-benzene-1,3-diol
    L3: 2-((E)-(2-(2-aminoethylamino)ethylimino)methyl)-6-ethoxy-phenol
    L4: 2-((E)-(3-(3-aminopropylamino)propylimino)methyl)-4-bromo-phenol
    L5: 2-((E)-(3-(3-aminopropylamino)propylimino)methyl)-4,6-dibromo-phenol

    Intradiol Dioxygenase Model iron(III) complexes with Catecholase Activity have been performed by UV-Vis spectrum in DMF solutions.The solutions are contained [Fe(L1~5)Cl2] which reacted with catecholate anions of 3,5-di-tert-butylcatechol(3,5-DTBC). The results show that the high lewis acidity of iron(III) complexes exhibits the higher Catecholase reactivity.The analytical results of electrical chemistry have the same as Catecholase reactivity.
    显示于类别:[化學學系暨研究所] 學位論文

    文件中的档案:

    档案 大小格式浏览次数
    0KbUnknown259检视/开启

    在機構典藏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 & TKU Library IR teams. Copyright ©   - 回馈