Chinese Journal of Magnetic Resonance ›› 2000, Vol. 17 ›› Issue (3): 183-190.

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NMR STUDIES FOR THE 1,2-DIHYDRO-4-PHENYL (2H)PHTHALAZINONE

MAO Shizhen1, ZHANG Tao1, YUAN Hanzhen1, CHENG Lin2, MIAO Xijia1   

  1. 1 State Key Lab. Magn. Reson. At. Mol. Phys., Wuhan Inst. Phys. and Math., The Chinese Academy of Sciences, Wuhan 430071;
    2 Wuhan Institute of Chemical Technology, Laboratory of advanced Aromatic Heterocyclic Materials, Wuhan 430074
  • Received:2000-02-16 Revised:2000-03-29 Published:2000-06-05 Online:2018-01-11

Abstract: A novel heterocyclic diamine, 1,2-dihydro-2-(4-amino-phenyl)-4-[4-(4-amino-phenoxyl) phenyl](2H)phthalazin-1-one was synthesized. Its 1H and 13C NMR spectra were completely assigned by utilizing the two-dimensional heteronuclear 13C-1Hmultiple-bond coherence(HMBC) spectroscopy, and heteronuclear 13C-1H one-bond coherence spectroscopy, homonuclear shift correlation spectroscopy(1H,1H-COSY) and the rotating frame overhauser enhancement spectroscopy(ROESY).The structure of the compound was proven to be phthalazinone instead of phthalazine ether.

Key words: Two-dimensional NMR, Phthalzinone, Assignment