Abstract
The 4-pyrazoline-3-one 1 reacts with 4-dimethylaminobenzaldehyde to yield the stable asymmetric cyanine dye 2b which reacts with 1 to give the colorless (aryl) (dipyrazolyl) methane 3b. Using aldehydes with less cationstabilizing groups the polymethines 2 are not isolated but only the methanes 3. The structures of 2b and 3 are discussed by1H,13C and Hetero NMR spectra.
| Translated title of the contribution | Synthesis and structure of pyrazolyl cations with polymethine and methane framework |
|---|---|
| Original language | German |
| Pages (from-to) | 219-225 |
| Number of pages | 7 |
| Journal | Monatshefte für Chemie Chemical Monthly |
| Volume | 114 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 1983 |
Keywords
- Cyanine dyes
- Dipyrazolylmethanes
- Heterocycles
- N-15-NMR
- O-17-NMR
- Phenazon