Chem. J. Chinese Universities ›› 2000, Vol. 21 ›› Issue (3): 386.

• Articles • Previous Articles     Next Articles

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

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

CLC Number: 

TrendMD: