Chinese Journal of Magnetic Resonance ›› 2020, Vol. 37 ›› Issue (4): 496-504.doi: 10.11938/cjmr20202803

• Short Communications • Previous Articles     Next Articles

Assignments of NMR Spectral Data of a Novel Carbazole-Triazinoindole Based N-Acylhydrazone Derivative

LI Ying-jun1, YANG Hong-jing1, LIU Ji-hong2, JIN Kun3, LIN Le-di1, LIU Xue-jie1   

  1. 1. College of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian 116029, China;
    2. Chemistry Analysis and Inspection Center, Dalian University of Technology, Dalian 116024, China;
    3. State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116023, China
  • Received:2020-01-19 Online:2020-11-05 Published:2020-03-23

Abstract: N-acylhydrazone compounds have two isomers, E/cis and E/trans, in polar solvents. In this work, 1H and 13C nuclear magnetic resonance (NMR) signals, coupling constants (J), and the spatial structures of the two isomers (E/cis and E/trans) of a novel carbazole-triazinoindole based N-acylhydrazone derivative 3, 2-(5H-[1,2,4] triazine[5,6-b]indol-3-ylthio)-N'-(9-ethylcarbazol-3-ylmethylene)acetylhydrazine, were obtained by one-dimensional and two-dimensional NMR techniques, infrared spectroscopy (IR) and elemental analysis. The ratios of the two isomers were determined.

Key words: nuclear magnetic resonance (NMR), assignment, 2D NMR, carbazole-triazinoindole, N-acylhydrazone derivative

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