210769-44-1Relevant academic research and scientific papers
N,N'-Ethylenebis(1-phenyl-3-methyl-4-acylpyrazoloneimine) derivatives: Synthesis and UV, IR, 1H and 13C NMR spectral studies
Uzoukwu, B. A.,Gloe, K.,Duddeck, H.
, p. 1180 - 1183 (2007/10/03)
N,N'-Ethylenebis(1-phenyl-3-methyl-4-acylpyrazoloneimine) derivatives have been synthesised and characterised using UV, IR, 1H and 13C NMR spectroscopy, where the substituents R(R')=CH3(H); CH3(CH3); CH3CH2(H); CH3CH2CH2(H). The spectral data show that the compounds behave in solution as quadridentate ligands and the bis(hydroxyimine) tautomer is the most stable tautomeric form in solution. The UV, IR, 1H and 13C NMR spectral assignments have been reported.
