A bambusuril macrocycle that binds anions in water with high affinity and selectivity
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- Keywords
- anion recognition, host-guest systems, macrocycles, self-assembly, supramolecular chemistry,
- MeSH
- Anions analysis isolation & purification MeSH
- Imidazoles chemical synthesis chemistry MeSH
- Macrocyclic Compounds chemical synthesis chemistry MeSH
- Models, Molecular MeSH
- Binding Sites MeSH
- Water analysis MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Anions MeSH
- bambus(6)uril MeSH Browser
- Imidazoles MeSH
- Macrocyclic Compounds MeSH
- Water MeSH
Synthetic receptors that function in water are important for the qualitative and quantitative detection of anions, which may act as pollutants in the environment or play important roles in biological processes. Neutral receptors are particularly appealing because they are often more selective than positively charged receptors; however, their affinity towards anions in pure water is only in range of 1-10(3) L mol(-1) . The anion-templated synthesis of a water-soluble bambusuril derivative is shown to be an outstanding receptor for various inorganic anions in pure water, with association constants of up to 10(7) L mol(-1) . Furthermore, the macrocycle discriminates between anions with unprecedented selectivity (up to 500 000-fold). We anticipate that the combination of remarkable affinity and selectivity of this macrocycle will enable the efficient detection and isolation of diverse anions in aqueous solutions, which is not possible with current supramolecular systems.
References provided by Crossref.org
Phase-transfer extraction for the fast quantification of perchlorate anions in water
Bambusuril analogs based on alternating glycoluril and xylylene units
Unsubstituted Bambusurils: Post-Macrocyclization Modification of Versatile Intermediates