Abstract
Four nano-baskets of calixarene including cone 25,27-di(carboxymethoxy)calix[4]arene-crown-5, 1,3-alternate 25,27-di[carboxymethoxy]-calix[4]arene-crown-5, cone 25,27-bis[carboxymethoxy]calix[4]arene-crown-6 and 1,3-alternate 25,27-di[carboxymethoxy]-calix[4]arene-crown-6 were synthesized and their binding abilities towards alkali and alkaline earth metals as well as some lanthanides were studied using differential pulse voltammetry. The novelty of this study was investigation of those macrocyclic complexes by voltammetric behaviors of two acidic moieties in each scaffold during complexation of crown ether ring. Their voltammetric behaviors were closely related to the complex formation by entrapment of cation into crown ether cavity and ion–dipole interaction between cation and acidic moieties in calixcrowns. The results revealed the selective changes in voltammetric behavior of synthesized scaffolds toward the cations. Moreover, the position of crown ether in 1,3-alternate instead of cone enhanced the domain of binding ability to more cations. Furthermore, it was shown that those carboxylic acid moieties, which were far from the crown ether ring in the 1,3-alternate, did not affected by encapsulated cations in the coordination space of crown ether and showed no voltammetric behavior.
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 callMore From: Journal of Inclusion Phenomena and Macrocyclic Chemistry
Disclaimer: 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.
