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RESEARCH PRODUCT
Anion Receptors Based on a Quinoline Backbone
Gerhard RaabeMarkus AlbrechtOlga OsetskaTriyantiStefanie SchiffersThomas WielandKari RissanenLuca Russosubject
chemistry.chemical_compoundChloroformchemistryStereochemistryOrganic ChemistryQuinolineSide chainHalidePhysical and Theoretical ChemistryReceptorSelectivityFluorideFluorescencedescription
2-Amido-8-urea substituted quinoline derivatives are potent receptors for the binding of halide or benzoate anions in chloroform. The selectivity and affinity of the receptors for fluoride can be tuned by variation of the substituents at the receptor side chains. Computational considerations show that the cleft of the receptors provides space for effective binding of F–, but not bigger anions.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2007-06-01 | European Journal of Organic Chemistry |