Chinese Journal of Magnetic Resonance ›› 1987, Vol. 4 ›› Issue (1): 35-46.

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ESR STUDY ON THE FREE RADICALS IN THE PHOTOCHEMICAL HYDROGEN ABSTRACTION REACTION BETWEEN THE N-SUBSTITUTED AMIDE AND BENZOPHENONE

Wang Wending1, Xu Guangzhi1, Sha Qinggui2   

  1. 1. Institute of Chemistry, Academia Sinica;
    2. Department of Chemistry, Qinghua University
  • Received:1986-07-27 Published:1987-03-05 Online:2018-01-22

Abstract: By use of spin trapping reagents, 2, 3,5,6-four metyl nitrosobenzene and phenyl t-butyl nitrone, in combination with ESR technique, the active free radicals were studied in the photochemical hydrogen abstraction reaction between benzophenone and twelve substituted amides, RC6H4NHC(O)CH3 (R=CH3, CI, Br, H, NO2), C6H5N(R)C(O)CH3 or HC(O)NR2(R=CH3, C2H5). The results show that:(1) for RC6H4NHC(O)CH3,benzophenone abstracts H from nitrogen to form RC6H4NC(O)CH3. (2)for C6H5N(R)C(O)CH3 or HC(O)NR2,benzophenone adstracts H from the methyl group linked with the carbonyl,from the carbony or from the carbon linked with nitrogen, respectively,to form C6H5N(R) C(O)CH2, C(O)NR2,C6H5N (CHR')C(O) CH3 or HC(O).

Key words: Benzophenone, Spin trapping, Photochemical abstraction reaction ESR, Free ridical