Abstract
Encapsulation of ion pairs in small spaces that are isolated from the medium is expected to result in amplified interactions between the ions. Yet, sequestration of ion pairs in self-assembled capsules is complicated by competition of the acids and bases for binding directly to the assembly components. We describe here a hydrogen-bonded capsule 1.2(8).1 that accommodates two γ-picolines and two acids as ion pairs. The supramolecular structure of the discrete 14-component assembly is characterized by NMR spectroscopy. The structure reveals the acids in the tapered ends of the capsule and γ-picoliniums near the glycoluril spacers in the capsule's center. Similar acid-base ion pairs are also obtained with 4-ethylpyridine, γ-picoline with difluoroacetic acid, and γ-picoline with trifluoromethanesulfonic acid. The (1)H NMR spectrum of the γ-picoline/trifluoroacetic acid ion pair shows a signal at δ = 18.7 ppm, indicating the acidic proton is in contact with both the picoline nitrogen and the trifluoroacetate oxygen. Further details about the unusual structures of ion pairs in small spaces are reported.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
