| Literature DB >> 22057428 |
Ángel L Fuentes de Arriba1, María G Turiel, Luis Simón, Francisca Sanz, Juan F Boyero, Francisco M Muñiz, Joaquín R Morán, Victoria Alcázar.
Abstract
Carbazole-based receptors functionalized with two sulfonamide groups have been synthesized and their properties as anion receptors have been evaluated. The receptor with bis(trifluoromethyl)aniline groups has shown a very high affinity for halide ions, especially remarkable as only two hydrogen bonds are formed in the complexes. (1)H NMR and fluorescence titrations have been carried out and binding constants up to 7.9 × 10(6) M(-1) have been reached. X-ray structures have been obtained and a modelling study has shown the possible reasons for the large affinity of these compounds for halide anions.Entities:
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Year: 2011 PMID: 22057428 DOI: 10.1039/c1ob06126g
Source DB: PubMed Journal: Org Biomol Chem ISSN: 1477-0520 Impact factor: 3.876