Novel self-assembling system based on resorcinarene and cationic surfactant

Mixed association of calix[4]resorcinarene with ethyl sulfonate groups on the lower rim and dimethylaminomethyl groups on the upper rim (CR) and cationic surfactant 4-aza-1-hexadecyl-azoniabicyclo[2.2.2]octane bromide (DABCO-16) is studied by methods of tensiometry, conductometry, potentiometry and...

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Bibliographic Details
Main Authors: Kashapov, Ruslan R., Pashirova, Tatiana N., Kharlamov, Sergey V., Ziganshina, Albina Yu., Ziltsova, Elena P., Lukashenko, Svetlana S., Zakharova, Lucia Ya., Habicher, Wolf D., Latypov, Shamil K., Konovalov, Alexander I.
Other Authors: Royal Society of Chemistry,
Format: Article
Language:English
Published: Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden 2014
Subjects:
nmr
Online Access:http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-138802
http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-138802
http://www.qucosa.de/fileadmin/data/qucosa/documents/13880/10.1039c1cp20906j.pdf
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Summary:Mixed association of calix[4]resorcinarene with ethyl sulfonate groups on the lower rim and dimethylaminomethyl groups on the upper rim (CR) and cationic surfactant 4-aza-1-hexadecyl-azoniabicyclo[2.2.2]octane bromide (DABCO-16) is studied by methods of tensiometry, conductometry, potentiometry and NMR spectroscopy at fixed CR concentration and varied surfactant concentration. Beyond ca. 0.4 mM of DABCO-16, mixed aggregates enriched by CR are proved to be formed due to electrostatic forces, while beyond ca. 5 mM, aggregates enriched by surfactant occur due to the hydrophobic effect. Spectrophotometry monitoring of the solubilization of a hydrophobic dye, Orange OT, demonstrated that only the second type of mixed aggregate enriched by DABCO-16 is capable of binding the organic probe, while the mixed system where the surfactant is a minor component shows no binding capacity towards Orange OT. This finding can be used for the design of nanocontainers with controllable binding/release properties. === Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.