高等学校化学学报 ›› 2000, Vol. 21 ›› Issue (3): 386.

• 论文 • 上一篇    下一篇

2-芳胺基-3H-1,3,4-噻二唑-5-硫醇类介离子化合物的X射线光电子能谱研究

张自义1, 褚长虎1, 孙小文1, 齐尚奎2, 李之春3, 廖仁安3   

  1. 1. 兰州大学应用有机化学国家重点实验室, 兰州 730000;
    2. 中国科学院兰州化学物理研究所, 兰州 730000;
    3. 南开大学元素有机化学国家重点实验室, 天津 300071
  • 收稿日期:1999-04-12 出版日期:2000-03-24 发布日期:2000-03-24
  • 通讯作者: 张自义(1933年出生),男,教授,博士生导师,主要从事杂环及杂原子化学研究.

Studies on X-ray Photoelectron Spectra of Meso-ionic Compound 2-Arylamino 1,3,4-thiadiazolium-5-thiolates

ZHANG Zi-Yi1, CHU Chang-Hu1, SUN Xiao-Wen1, QI Shang-Kui2, LI Zhi-Chun3, LIAO Ren-An3   

  1. Department of Chemistry, National Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000;
    2. ChinaLaboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Science, Lanzhou 730000;
    3. ChinaState Key Laboratory of Elemento Organic Chemistry, Nankai University, Tianjin 300071, China
  • Received:1999-04-12 Online:2000-03-24 Published:2000-03-24

摘要: 用XPS表征2-芳胺基-1,3,4-噻二唑-5-硫酮(1)在ω-溴代-ω-(1H-1,2,4-三唑)-苯乙酮诱导下生成的2-芳胺基-3H-1,3,4-噻二唑-5-硫醇类介离子化合物(4).结果表明,化合物4分子中的C1s,N1s,S2p电子结合能均高于化合物1,尤其以N1s,S2p结合能谱最为特征.例如在含3个氮原子的化合物4中由于噻二唑环的两个氮环境不同,故产生3个峰,而在与其结构相近的对照物1中,由于噻二唑环的两个氮环境相近,故产生2个峰.S2p诸状态结合能加合值化合物4均大于化合物1,在化合物4中均是杂环内硫大于杂环外硫.

关键词: X射线光电子能谱(XPS), 1, 3, 4-噻二唑-5-硫醇, 介离子化合物

Abstract: The structures of 2-arylamino-1,3,4-thiadiazolium-5-thiolates(4) were confirmed by Xray photoelectron spectra. The meso ionic were prepared from 2-arylamino 1,3,4-thiadiazol-5-thiones by using ω-bromo-ω-(1H-1,2,4-triazol-1-yl)acetophenone(2). The results showed that the binding energies of C1s, N1s , and S2p in meso-ionic 4 are greater than those in the correspondence compounds 1, which were more obvious in N1s and S2p . For example, N1s showed three signals in mesoionic 4 and only two signals and in compounds 1 because the chemical environment of thiadiazole rings two nitrogen atoms are different in4 and same in1. Furthermore, the additive binding energy of S2p in ring is greater than the exocyclic one for the same mesoionic 4.

Key words: X-ray photoelectron spectra, 1,3,4-Thiazolium-2-thiolates, Meso-ionic

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