Chem. J. Chinese Universities ›› 2012, Vol. 33 ›› Issue (03): 496.doi: 10.3969/j.issn.0251-0790.2012.03.012

• Organic Chemistry • Previous Articles     Next Articles

Synthesis and Characterization of Bis-porphyrins with Different Substituents

SUN Yuan-Yuan, SHAN Ning, WANG Bin-Bin, LIAN Wen-Hui, YU Miao, SHI Tong-Shun   

  1. College of Chemistry, Jilin University, Changchun 130021, China
  • Received:2011-07-16 Online:2012-03-10 Published:2012-03-10

Abstract:

Bis-porphyrins with different substituents were synthesized via the linkage of (E)-2-butenedioyl dichloride and characterized by IR, UV-Vis, 1H NMR and MS spectra. Also, their spectroscopic properties were studied by SPS, fluorescence spectra and Raman spectra. The results show that the substituents have great influences on the quantum yield of fluorescence, the methoxy groups increase the intensity and the quantum yield of the porphyin while the chloric groups decrease them. This suggests that electron-withdrawing groups(-Cl) have stronger influence on fluorescence property of porphyrin than electron-donating groups(-OCH3). The electronic effects of substituent group influence on the Raman spectra of porphyrin dimers are also great.

Key words: (E)-2-Butenedioyl dichloride, Bis-porphyrins, Raman spectrum, Fluorescence spectrum, Substituent effect

CLC Number: 

TrendMD: