| Autor: |
Brunetti E; Laboratoire de Chimie Organique, Université Libre de Bruxelles (ULB) , Avenue F.D. Roosevelt 50, CP160/06, B-1050 Brussels, Belgium., Picron JF, Flidrova K, Bruylants G, Bartik K, Jabin I |
| Jazyk: |
angličtina |
| Zdroj: |
The Journal of organic chemistry [J Org Chem] 2014 Jul 03; Vol. 79 (13), pp. 6179-88. Date of Electronic Publication: 2014 Jun 24. |
| DOI: |
10.1021/jo5009146 |
| Abstrakt: |
The association of a concave macrocyclic compound to one or multiple fluorophores is an appealing strategy for the design of chemosensors. Indeed, as with biological systems, a cavity-based selectivity can be expected with such fluorescent receptors. Examples of calix[6]arene-based systems using this strategy are rare in the literature, and to our knowledge, no examples of fluorescent receptors that can bind organic contact ion pairs have been reported. This report describes the straightforward synthesis of fluorescent calix[6]arene-based receptors 4a and 4b bearing three pyrenyl subunits and the study of their binding properties toward anions and ammonium salts using different spectroscopies. It was found that receptor 4a exhibits a remarkable selectivity for the sulfate anion in DMSO, enabling its selective sensing by fluorescence spectroscopy. In CDCl3, the receptor is able to bind ammonium ions efficiently only in association with the sulfate anion. Interestingly, this cooperative binding of ammonium sulfate salts was also evidenced in a protic environment. Finally, a cavity-based selectivity in terms of size and shape of the guest was observed with both receptors 4a and 4b, opening interesting perspectives on the elaboration of fluorescent cavity-based systems for the selective sensing of biologically relevant ammonium salts such as neurotransmitters. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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