## Abstract magnified image __O__βphenyleneβdiamine derivative containing colorimetric dinitroquinoxaline has been synthesized. Its UVβvis spectroscopy and ^1^H NMR investigation reveal that the receptor shows the strong binding ability for AcO^β^, F^β^, and H~2~PO, moderate binding abilities for
Anion recognition properties of the neutral receptors bearing amide macrocycle
β Scribed by X.-F. Shang; Z.-S. Cai; H.-K. Lin; H. Lin
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2008
- Tongue
- English
- Weight
- 382 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-152X
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β¦ Synopsis
Abstract
magnified image
Neutral classes of amideβbased macrocycle have been synthesized and the anion binding abilities are assessed by UVβvis titration and ^1^H nmr experiments. Results indicate that higher anion binding abilities are observed for H~2~PO~4~^β^, F^β^ and AcO^β^, but almost no affinity for Cl^β^, Br^β^, I^β^ and OH^β^. The ^1^H nmr spectra shows that the interactions between the receptors and fluoride anion depend on two factors, respectively: one is depend on hydrogen bonding, the other on deprotonation.
π SIMILAR VOLUMES
Two new neutral receptors (1 and 2) containing (thio)urea and amide groups were synthesized by simple steps in g o d yields. The binding properties for anions of 1 and 2 were characterized by W-vis and fluorescence spectra. Receptor 1 had 811 excellent selectivity for A&-in comparison with other ani