## Abstract ^13^C and ^1^H NMR spectra of six Schiff bases formed from 2‐hydroxy‐1‐naphthaldehyde and substituted anilines were measured and assigned in a variety of solvents. Based on the ^13^C chemical shifts and ^3^__J__(CH,NH), the ratio of the keto‐amine and phenol‐imine tautomers was derived
Schiff Bases from TRIS and ortho-Hydroxyarenecarbaldehydes: Structures and Tautomeric Equilibria in the Solid State and in Solution
✍ Scribed by R. Fernando Martínez; Martín Ávalos; Reyes Babiano; Pedro Cintas; José L. Jiménez; Mark E. Light; Juan C. Palacios
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 856 KB
- Volume
- 2011
- Category
- Article
- ISSN
- 1434-193X
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## Abstract New Schiff bases and new hydrazones were synthesized and studied by ^13^C and ^15^N CP/MAS spectroscopy and by ^1^H^1^H COSY, ^1^H^13^C HMBC, ^1^H^13^C HSQC, ^1^H^15^N HMQC and ^1^H^15^N HSQC correlations. The CP/MAS investigation of gossypol has demonstrated that in the solid stat
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