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Table 5 1H and 13C NMR signals of OBH and its diamagnetic complexes

From: Spectral, thermal, molecular modeling and biological studies on mono- and binuclear complexes derived from oxalo bis(2,3-butanedionehydrazone)

Compound

NH

CH3

13C signals

OBH

11.924 (s, 2H)

2.129 (s, 6H)

196.65 (C=O)ketonic

167.58; (C=O)amidic

148.81 (C=N)

23.90 (CH3)

[Zn(OBH–H)2]

11.781 (s, 1H)

11.565 (s, 1H)

2.371 (s, 3H)

2.118 (s, 3H)

196.68 (C=O)ketonic

168.02 (C=O)amidic free

166.21 (C=O)amidic bonded

149.44 (C=N), (C=N)*

23.94 (CH3)

[VO(OBH-H)2]·H2O

11.769 (s, 1H)

2.087 (s, 3H)

2.053 (s, 3H)

197.12 (C=O)ketonic

172.50 (C=O)amidic (free)

168.44–167.47 (C=O)amidic (bonded)

149.60–148.86 (C=N), (C=N)*

124.68 (C–O)

24.68; 24.98 (CH3)

[Pd2(OBH)(H2O)2Cl4]·2H2O

11.766 (s, 1H)

11.566 (s, 1H)

2.290 (s, 6H)

196.75 (C=O)ketonic

167.98; (C=O)amidic

148.88 (C=N)

22.90 (CH3)

  1. *New azomethine group as a result of enolization