New fluorescent bis-β-cyclodextrin-indolizine sensor. Synthesis and sensing ability
✍ Scribed by Georgiana G. Surpateanu; David Landy; Neculai C. Lungu; Sophie Fourmentin; Gheorghe Surpateanu
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2007
- Tongue
- English
- Weight
- 368 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
magnified image
The synthesis of 1,3‐[bis‐N‐6A‐deoxy‐β‐cyclodextrin‐6A‐yl‐aminocabonyl]‐7‐pyridin‐4‐yl indolizine is reported. The reaction proceeds by an amidation between 6‐amino‐β‐cyclodextrin and 1,3‐[bis‐(‐4‐nitrophenoxycarbonyl)‐7‐[pyridine‐4‐yl)] and yields the first sensor having in its structure the fluorescent indolizine and two β‐cyclodextrin fragments. The sensing ability towards phenol, p‐cresol and adamantan‐1‐ol has been evaluated by fluorescence spectroscopy. The molecular modelling study realised by MM3 and AM1 methods shows that non cooperative conformations are favoured, thus explaining that inclusion ability is not increased by such dimer, and that sensitivity is not enhanced as compared to corresponding monomeric sensors.
📜 SIMILAR VOLUMES
## Abstract A novel 4,4′‐sulfonyldianiline‐bridged bis(__β__‐cyclodextrin (CD)) **2** was synthesized, and its complex stability constants (__K__~s~) for the 1 : 1 inclusion complexation with bile salts, __i.e.__, cholate (CA), deoxycholate (DCA), glycocholate (GCA), and taurocholate (TCA) have bee