高等学校化学学报 ›› 1998, Vol. 19 ›› Issue (7): 1026.

• 研究简报 • 上一篇    下一篇

四(α-萘基)四苯并卟啉钴配合物的光谱电化学性质

师同顺1, 张旭光2, 柳巍1, 贾伯文1, 刘国发1   

  1. 1. 吉林大学化学系, 长春, 130023;
    2. 吉林工业大学电子系, 长春, 130024
  • 收稿日期:1997-07-10 出版日期:1998-07-24 发布日期:1998-07-24
  • 通讯作者: 师同顺,男,52岁,副教授.
  • 作者简介:师同顺,男,52岁,副教授.
  • 基金资助:

    国家自然科学基金(批准号:79783001)和吉林省科委科学基金资助课题.

Spectroelectrochemical Characteristics of Tetra-(α-naphythyl) Tetrabenzoporphyrin Cobalt Complex

SHI Tong-Shun1, ZHANG Xu-Guang2, LIU Wei1, JIA Bai-Wen1, LIU Guo-Fa1   

  1. 1. Department of Chemistry, Jilin University, Changchun, 130023;
    2. Department of Electronics, Jilin Industry University, Changchun, 130024
  • Received:1997-07-10 Online:1998-07-24 Published:1998-07-24

摘要: Kelet等[1]研究CoTMAPI催化水制取氢气的反应时指出,活性中心是一价钴卟啉。曹锡章等[2]研究钴卟啉催化CO2电化学还原时指出,活性中心也是一价钴卟啉。然而,不稳定价态的金属卟啉配合物的制备和性质研究较为困难。

关键词: 四(&alpha, -萘基)四苯并卟啉, 循环伏安法, 现场紫外可见光谱电化学, 现场红外光谱电化学

Abstract: The electrochemical and spectroelectrochemical behaviour of tetra (α-naphythyl) tetrabenzoporphyrin cobalt complex, TNTBPCo, was studied by cyclic voltammetry, in situ FTIR and in situ UV-V is spectroelectrochemistry. The different oxidation states of the complex were obtained by controlling potential electrolysis at different potentials, and this electronic spectra and molecular vibration spectra were studied. The first and second redox processes of TNTBPCo(Ⅱ) correspond to the centre metal cobalt(Ⅱ) to form TNTBPCo(Ⅲ)+or TNTBPCo(Ⅰ)-. The third reduction step is the addition of one electron to the porphyrin ring. The Soret band of TNTBPCo moves to low wavelength as the oxidation state of the complex decreases. The oxidation state sensitive bands of TNTBPCo were found to be in the 1660, 1476, 1142, 924 and 998 cm-1and these bands shift to low frequency as the oxidation state of the centre metal decreases.

Key words: Tetra-(α-naphythyl)tetrabenzoporphyrin cobalt complex, Cyclic voltammetry, In situ UV-V is spectroelectrochemistry, In situ FTIR spectroelectrochemistry

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