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Tautomerism in Schiff bases. The cases of 2-hydroxy-1-naphthaldehyde and 1-hydroxy-2-naphthaldehyde investigated in solution and the solid state

✍ Scribed by Martínez, R. Fernando; Ávalos, Martín; Babiano, Reyes; Cintas, Pedro; Jiménez, José L.; Light, Mark E.; Palacios, Juan C.

Book ID
118201256
Publisher
Royal Society of Chemistry
Year
2011
Tongue
English
Weight
627 KB
Volume
9
Category
Article
ISSN
1477-0520

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Tautomerism in 2-hydroxy-1-naphthaldehyd
Tautomerism in 2-hydroxy-1-naphthaldehyde schiff bases in solution and the solid state investigated using 13C NMR spectroscopy
✍ S. R. Salman; J. C. Lindon; R. D. Farrant; T. A. Carpenter 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 282 KB

## 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