Open-Chain Dications and Betaines with Imidazolium Molecular Motifs: Synthesis and Structural Aspects
✍ Scribed by Ermitas Alcalde; Neus Mesquida; Montserrat Alemany; Carmen Alvarez-Rúa; Santiago García-Granda; Pedro Pacheco; Lluïsa Pérez-García
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 535 KB
- Volume
- 2002
- Category
- Article
- ISSN
- 1434-193X
No coin nor oath required. For personal study only.
✦ Synopsis
The synthesis of trinuclear open-chain prototypes gave variable yields: Ͼ 53% for dications 1•2X and 2•2X and Ͼ 80% for proton-ionizable dications 3•2X-5•2X incorporating 1H-1,2,4-triazole moieties. Deprotonation of the latter compounds resulted in the formation of the betaine counterparts 13•X-15•X. The courses of the dequaternization reactions of compounds 4•2X and 5•2X were also studied. The structural properties of dicationic protophanes 1•2X and 2•2X, containing bis(imidazolium) motifs, were examined by 1 H and [ ‡] Heterocyclic Betaines, 47. Ϫ Part 46: Ref. [1a] [a]
📜 SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v