C-13 NMR substituent-induced chemical shifts in 4-(substituted phenyl)-3-phenyl-1,2,4-oxadiazol-5(4H)-ones (thiones)

Kara Y. S.

SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, cilt.149, ss.920-927, 2015 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 149
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1016/j.saa.2015.04.081
  • Dergi Adı: SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.920-927
  • Anahtar Kelimeler: Oxadiazole ring, SSP analyses, DSP analyses, DSP-NLR analyses, Reverse substituent effect, Hammett correlation, FREE-ENERGY RELATIONSHIPS, 1,3,4-OXADIAZOLE DERIVATIVES, QUANTITATIVE TREATMENT, MAGNETIC-RESONANCE, 1,2,4-OXADIAZOLE, TRANSMISSION, ANTIOXIDANT, POLARIZATION, PROPAGATION, AMIDOXIMES
  • Kocaeli Üniversitesi Adresli: Evet

Özet

In the present, study mostly novel ten 4-(substituted phenyl)-3-phenyl-1,2,4-oxadiazol-5(4H)-ones and ten 4-(substituted phenyl)-3-phenyl-1,2,4-oxadiazol-5(4H)-thiones were synthesized. These oxadiazole derivatives were characterized by IR, H-1 NMR, C-13 NMR and elemental analyses. Their C-13 NMR spectra were measured in Deuterochloroform (CDCl3). The correlation analysis for the substituent-induced chemical shift (SCS) with Hammett substituent constants (sigma), Brown Okamoto substituent constants (sigma(+), sigma(-)), inductive substituent constants (sigma(1)) and different of resonance substituent constants (sigma(R), sigma(o)(R)) were performed using SSP (single substituent parameter), DSP (dual substituent parameter) and DSP-NLR (dual substituent parameter-non-linear resonance) methods, as well as single and multiple regression analysis. Negative rho values were found for all correlations (reverse substituent effect). The results of all statistical analyses, C-13 NMR chemical shift of C=N, C=O and C=S carbon of oxadiazole rings have shown satisfactory correlation. (C) 2015 Elsevier B.V. All rights reserved.