Abstract
The carbon-13 NMR chemical shifts of a series of substituted 2-hydroxy-1-naphthaldehyde compounds, together with those of two model Schiff bases, are presented. The data for the two model compounds, salicylidine benzylamine and naphthalidine amino quinoline, were used to calculate the percentage keto form in substituted 2-hydroxy-1-naphthaldehyde.
| Original language | English |
|---|---|
| Pages (from-to) | 9-13 |
| Number of pages | 5 |
| Journal | Canadian Journal of Analytical Sciences and Spectroscopy |
| Volume | 42 |
| Issue number | 1 |
| Publication status | Published - 1997 |
| Externally published | Yes |
ASJC Scopus subject areas
- Analytical Chemistry
- Atomic and Molecular Physics, and Optics
- Spectroscopy
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