Synthesis, binding properties and theoretical studies of p-tert-butylhexahomotrioxacalix[3]arene tri(adamantyl)ketone with alkali, alkaline earth, transition, heavy metal and lanthanide cations |
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Authors: | Paula M. Marcos,José R. Ascenso,Raul J. Bernardino |
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Affiliation: | a Centro de Ciências Moleculares e Materiais, Faculdade de Ciências da Universidade de Lisboa, Edifício C8, 1749-016 Lisboa, Portugal b Faculdade de Farmácia da Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003 Lisboa, Portugal c Instituto Superior Técnico, Complexo I, Av. Rovisco Pais, 1049-001 Lisboa, Portugal d Escola Superior de Tecnologia do Mar, Instituto Politécnico de Leiria, Santuário N.a Sra. dos Remédios, Apartado 126, 2524-909 Peniche, Portugal e School of Pharmacy and Biomolecular Sciences, University of Brighton, Brighton BN2 4GJ, UK |
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Abstract: | p-tert-Butylhexahomotrioxacalix[3]arene tri(adamantyl)ketone (1b) was synthesized for the first time. Compound 1b was obtained in a cone conformation in solution at room temperature, as established by NMR spectroscopy (1H and 13C). The binding properties of ligand 1b for alkali, alkaline earth, transition, heavy metal and lanthanide cations have been assessed by phase transfer and proton NMR titration experiments. Molecular mechanics and ab initio techniques were also employed to complement the NMR data. The results are compared to those obtained with other closely related homooxacalixarene derivatives. Although triketone 1b is a weak extractant, it shows a strong peak selectivity for Na+ and also some preference for Ag+. Proton NMR titrations indicate the formation of 1:1 complexes between 1b and the cations studied, and also that they should be located inside the cavity defined by the phenoxy and carbonyl oxygen atoms. Although the molecular mechanics results show little correlation with the NMR data, a good agreement was obtained with the ab initio models. |
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Keywords: | Calixarenes Hexahomotrioxacalix[3]arene ketone Metal cation extraction Proton NMR titration Molecular mechanics Ab initio |
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