Articles

Spectroscopic, Electrochemistry and Thermal Properties of Monoand 1,1'-Disubstituted 1,2,3-Triazolylferrocene Derivatives

  • Qian Chao ,
  • Chuo Luopeng ,
  • Zhao Haiying ,
  • Bian Zhanxi
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  • College of Chemistry and Chemical Engineering, Inner Mongolia University, Inner Mongolia Key Laboratory of Fine Organic Synthesis, Hohhot 010021

Received date: 2017-03-29

  Revised date: 2017-04-27

  Online published: 2017-05-17

Supported by

Project supported by National Natural Science Foundation of China (No. 21562032), the Research Program of Science and Technology at Universities of Inner Mongolia (No. NJZZ001) and the Natural Science Foundation of Inner Mongolia (Nos. 2013MS0207).

Abstract

A series of mono-and 1,1'-disubstituted 1,2,3-triazolylferrocene derivatives have been synthesized and characterized. In UV-Vis spectroscopy, 1,1'-disubstituted compounds have the larger molar absorption coefficient than those of monosubstituted compounds. The fluorescence intensity weakened with increasing the number of alkoxy chain and further weakened after introduction of the highly electronegative chlorine atom. All new compounds showed quasireversible redox process. The potentials for 1,1'-disubstituted 1,2,3-triazolylferrocene derivatives anodically shifted about 150 mV compared with those of monosubstituted compounds, indicating harder oxidation by loss of an electron for the former. These compounds started to decompose at about 285~305℃. The 1,2,3-triazolylferrocene derivative with one terminal alkoxy chain had high melting point, and suffered from degradation reaction before changing into isotropic liquid, and those with multiterminal alkoxy chains showed either simple melting and freezing process or crystal polymorphic phase to isotropic liquid phase transitions in the heating and cooling cycles.

Cite this article

Qian Chao , Chuo Luopeng , Zhao Haiying , Bian Zhanxi . Spectroscopic, Electrochemistry and Thermal Properties of Monoand 1,1'-Disubstituted 1,2,3-Triazolylferrocene Derivatives[J]. Chinese Journal of Organic Chemistry, 2017 , 37(9) : 2328 -2335 . DOI: 10.6023/cjoc201703049

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