高等学校化学学报 ›› 1995, Vol. 16 ›› Issue (9): 1415.

• 论文 • 上一篇    下一篇

多组份氧化还原体系的双二茂铁酰基硫脲及其铜配合物

王积涛, 许育明, 袁耀锋, 王斌, 杨永安, 叶素明   

  1. 南开大学化学系, 天津, 300071
  • 收稿日期:1994-11-25 修回日期:1995-03-25 出版日期:1995-09-24 发布日期:1995-09-24
  • 通讯作者: 袁耀锋
  • 作者简介:王积涛,男,76岁,教授,博士导师.
  • 基金资助:

    国家自然科学基金;南开大学元素有机化学国家重点实验室基金

Multicomponent Redox Systems Consisting of N-Ferrocenoyl-N'-ferrocenyl (ethylferrocene) Thiourea and Its Copper (Ⅱ) Complexes

WANG ji-Tao, XU Yu-Ming, YUAN Yao-Feng, WANG Bin, YANG Yong-An, YE Su-Ming   

  1. Department of Chemistry, Nankai University, Tianjin, 300071
  • Received:1994-11-25 Revised:1995-03-25 Online:1995-09-24 Published:1995-09-24

摘要: 利用不等价双二茂铁酰基硫脲多齿配体与氧化铜、醋酸铜反应合成了4个新型多核配合物,提出了配位模型。总结了配位前后IR、1HNMR的变化特征,并对它们的电化学性质进行了研究,发现2个配体中均含有2个不等价二茂铁,属于多组份氧化还原体系,但其与CuCl2、CuAc2形成多核配合物的电化学性质却呈现出平均化趋势,提出了相应的转化机理。

关键词: 酰基硫脲, 二茂铁衍生物, 多组份氧化还原体系, 循环伏安

Abstract: The two non-equivalent ferrocene fragments N-ferrocenoyl-N'-ferrocenyl thiourea (HL1) and N-ferrocenoyl-N'-ethylferrocene thiourea (HL2)are prepared by the addition of ferrocenoyl isothiocyanate with aminoferrocene and aminoethylferrocene respectively. The copper (Ⅱ) complexes of these ligands are isolated and have been characterized by elementary analyses and spectral (IR, 1HNMR) measurements. The redox behavior of the two ligands and their complexes is investigated by cyclic voltammeter.The legends(HL1,HL2) undergo two distinct and consecutive reversible oneelectron oxidation processes centred on the two non-equivalent ferrocene fragments, but in complex Cu(HL1)2Cl2, it is able to release two electrons at the same potentials.The two ferrocenyl groups change to equivalent ferrocene fragments.In the complex Cu(L2)Ac,it is still able to release two electrons at distinctly different potentials,Ep1, and Ep2.Ep1, and Ep2 values are chaning to close, such an approch is quite interesting. Some factors affecting the magnitude of the potential separation △E(△E=Ep2-Ep1) are envisaged.

Key words: Aeylthiourea, Ferrocene derivative, Multicomponent redox system, Cyclic voltammetry

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