Abstract
The X-ray crystal structures of trans-6,13-dimethyl-6,13-diamino-1,4,8,11-tetraazacyclotetradecane hexahydrochloride dihydrate (trans-diammac.6HCl.2H(2)O) and the product 1 derived by condensation of trans-diammac with pyridine-2-carboxaldehyde, have been determined. For 1 intramolecular attack of macrocycle amine nitrogen atoms on the C=N bonds of the intermediate diimine gives a ring-closed tautomeric form, which comprises two imidazolidine rings fused to the macrocycle.
| Original language | English |
|---|---|
| Pages (from-to) | 234-236 |
| Number of pages | 3 |
| Journal | Journal of Chemical Research |
| Issue number | 3 |
| Publication status | Published - Mar 2004 |
Keywords
- macrocycle
- diammac
- X-ray crystallography
- NMR
- METAL-IONS
- LIGAND
- COBALT(III)
- COMPLEXES
- CATIONS
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