Chinese Journal of Magnetic Resonance ›› 1987, Vol. 4 ›› Issue (4): 345-354.

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ESR STUDY OF ACTIVE RADICALS PRODUCED IN THE PHOTOCHEMICAL HYDROGEN ABSTRACTION REACTIONS BETWEEN BENZOPHENONE AND 2-ARYL-1,3-DITHIOLAN

Ji Haixing1, Xu Guangzhi1, Sun Lijun2, Shi Shujian2   

  1. 1. Institute of Chemistry, Academia Sinica, Beijing;
    2. Beijing Institute of Chemical Technology
  • Received:1987-04-01 Published:1987-12-05 Online:2018-01-22

Abstract: The active radicals produced in the photochemical hydrogen abstraction reactions between benzophenone and 2-ary1-1, 3-dithiolan were studied by combination of spin trapping technique with ESR specroscopy. Results show that the homolytic cleavage of C-H on the 2-C (or 4-C, 6-C) could take place, the produced active radicals  CH2 werestabilized by the conjugation of adjacent sulphur atoms and could be trapped by nitrosodurene (ND) (or 2,4,6-tri-t-butylnitrosobenzene(TBN)) to form two spin adducts the concentration ratio of which was about 1:1.

Key words: Spin trapping technique, 2-aryl-1,3-dithiolan, Radical, Photochemical hydrogen abstraction reaction, ESR