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13 C NMR and azomethine 1 H NMR spectra of substituted N ‐benzylideneanilines and hammett correlations
Author(s) -
Echevarria Aurea,
Miller Joseph,
Nascimento M. Graça
Publication year - 1985
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/mrc.1260231005
Subject(s) - chemistry , nmr spectra database , carbon 13 nmr , carbon atom , spectral line , proton nmr , chemical shift , carbon 13 nmr satellite , medicinal chemistry , stereochemistry , nuclear magnetic resonance spectroscopy , crystallography , fluorine 19 nmr , organic chemistry , ring (chemistry) , physics , astronomy
Twenty‐four N ‐benzyliaeneanilines (four being new compounds) have been prepared, which are divided conveniently into three series: (I) with 4‐substituents, plus one compound with 3‐ and 4‐substituents; (II) with 4′‐substituents, plus one compound with 3′‐ and 4′‐substituents; and (III) with 4‐ and 4′‐substituents. Their 13 C NMR spectra and the 1 H NMR absorption of the hydrogen attached to the imidoyl carbon atom have been studied and their Hammett correlations were tested.

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