Chinese Journal of Magnetic Resonance ›› 1989, Vol. 6 ›› Issue (2): 239-244.

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STUDY OF 13C-NMR SPECTRA FOR THE COMPOUNDS OF 1-(4-PYRIDINE ACYL)-4-ARYL THIOSEMICARBAZIDE AND 3-(4-PYRIDINE)-4-AROMATIC-1,2,4-TRIAZOLINE-5-THIONE

Song Maosen, Liu Peiqi, Zhang Ziyi, Yang Kexin   

  1. Department of chemistry, Lanzhou University
  • Received:1988-03-23 Revised:1988-06-30 Published:1989-06-05 Online:2018-01-22

Abstract: The carbon-13 NMR spectra of 1-(4-pyridine acyl)-4-phenyl thioscmicarbazide, 1-(4-pyridine acyl)-4-p-chlorO-phenylthiosemicarbazide, 1-(4-pyridine acyl)-4-p-bromo-phenylthiosemicarba/ide, 3-(4-pyridinyl)-4-phenyl-1, 2, 4-triazoline-5-thionc, 3-(4-pyridinyl)-p-chloro phenyl-1, 2, 4-triazoline-5-thione, 3-(4-pyridinyl)-p-bromo phenyl-1, 2, 4-triazoline-5-thione and their derivatives were studied in this paper. The chemical shifts of various carbon resonance peaks were assigned by the proton-noise decoupling, Off-resonance, APT-technique, and use of empirical methods. At the same time, the substituent effects of 4-hydrazide in monosubstituted pyridinc were obtained. These parameters are Z42 (Z46) 0.1ppm Z43 (Z45)-3.3ppm and Z44 3.9ppm (solvent:polysol; reference:TMS).

Key words: The effect of substituent, 13C-NMR