Chem. J. Chinese Universities ›› 1993, Vol. 14 ›› Issue (2): 257.

• Articles • Previous Articles     Next Articles

The Influence of Molecular Configuration and Substltuent Electron Effect on 13C NMR Spectra of Diethyl 2,3-Dicyano-2,3-di(p-X substituted phenyl)succinate

YANG Di-Lun, QI Chen-Ze, WU Jing-Jia, CUI Yu-Xin, LIU You-Cheng   

  1. Department of Chemistry, Lanzhou University, Lanzhou, 730000
  • Received:1992-06-05 Revised:1992-07-14 Online:1993-02-24 Published:1993-02-24

Abstract: Meso- and dl-diethyl 2, 3-dicyano-2, 3-di(p-Xsubstituted phenyl)succinates(X=OCH3, CH3, H, Cl, NO2) are studied by means of 13C NMRspectra, The results indicate that the chemical shifts of carbon atoms in the same group on both sides of central carbon-carbon bond are equivalent, and the chemical shifts of C7-C9 atoms in the dl-isomers are smaller than that in corresponding meso-isomers.The average difference Δδβ-menvare found to be 1.80±0.16 ppm for C7, 0.39±0.16 ppm for C8 and 0.23±0.16 ppm for C9 respectivly.The plots of chemical shifts of C6, C7 and C8 atoms versus Hammett constant σ of substituents on p-position of benzene ring are good in linear line.

Key words: Diethyl2, 3-dicyano-2, 3-di(p-X substituted phenyl)succinate, 13C NMR chemical shift, Hammett substitutent constant

TrendMD: