Journal
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2
Volume -, Issue 5, Pages 808-814Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b008603g
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Isomerically pure 4,5',4,5'-tetra-tert-butyltetrabenzo-24-crown-8 was synthesized by a route that eliminates any need for isomer separation. Its structure was determined using single crystal X-ray diffraction methods. Since the observed saddle-shaped conformation of the crown ether is the same as previously reported for the closely related tetrabenzo-24-crown-8, the presence of the peripheral tert-butyl groups has no apparent effect on ring structure. This structure experiences few intermolecular interactions beyond London forces, suggesting it represents a low energy conformation. Liquid-liquid distribution behavior of CsNO3 and CsClO4 between water and 1,2-dichloro-ethane (1,2-DCE) containing 4,5',4,5'-tetra-tert-butyltetrabenzo)-24-crown-8 was investigated. Equilibrium constants corresponding to the extraction of ion pairs and dissociated ions, formation of the caesium complex, and dissociation of the ion pairs in water-saturated 1,2-DCE at 25 degreesC were obtained from equilibrium modeling using the SXLSQI program. 4,5',4,5'-Tetra-tert-butyltetrabenzo-24-crown-8 exhibits stronger caesium binding and a similarly low tendency towards ion-pairing, in comparison with the previously characterized isomeric 4,4'- and 4,5'-di-tert-octyltetrabenzo-24-crown-8 ethers.
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