Chem. J. Chinese Universities ›› 2003, Vol. 24 ›› Issue (7): 1231.

• Preface • Previous Articles     Next Articles

Effect of Functional Groups on the Activity of Water-soluble β-Alanine C60Derivatives for Superoxide Anion Radical Scavenging

SUN Tao, XU Zhu-De, JIA Zhi-Shen   

  1. Department of Chemistry, Yuquan Campus, Zhejiang University, Hangzhou 310027, China
  • Received:2002-01-12 Online:2003-07-24 Published:2003-07-24

Abstract: Three water-soluble β-alanine C60 adducts with different addition numbers, C60(NHCH2CH2COONa) nH n(n=1,5,9), were synthesized. The products were characterized by FTIR, 1HNMR and elemental analysis. The antioxidant activity of these C60 adducts as the quencher for superoxide anion radical O2 was evaluated by chemiluminescence in the system of pyrogallol-luminol. The results indicate that the three C60 derivatives are all excellent quencher for superoxide anion radical O2. The concentrations of 50% inhibition are 252, 140, 112 μmol/L respectively. This high efficiency should be attributed to many factors such as the numbers of remaining double bonds, donor effect of amino group and steric effect. However, the above results also suggest the effect of the adducted β-alanine groups is predominated in this system.

Key words: β-Alanine C60 derivatives, Superoxide anion radical O2, Auto-oxidation of pyrogallol, Chemiluminescence

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