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Anion Recognition by Diureido-calix[4]arenes in the 1,3-Alternate Conformation

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    SYSNO ASEP0332779
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleAnion Recognition by Diureido-calix[4]arenes in the 1,3-Alternate Conformation
    TitleAniontové rozpoznání diureido-calix[4]arenů v 1,3-střídavé konformaci
    Author(s) Cuřínová, Petra (UCHP-M) RID, SAI, ORCID
    Stibor, I. (CZ)
    Budka, J. (CZ)
    Sýkora, Jan (UCHP-M) RID, ORCID, SAI
    Lang, Kamil (UACH-T) SAI, RID, ORCID
    Lhoták, P. (CZ)
    Source TitleNew Journal of Chemistry. - : Royal Society of Chemistry - ISSN 1144-0546
    Roč. 33, č. 3 (2009), s. 612-619
    Number of pages8 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordscomplexation ability ; biological systems ; anions
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsGA203/06/0738 GA ČR - Czech Science Foundation (CSF)
    GA203/07/1424 GA ČR - Czech Science Foundation (CSF)
    IAA400720706 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z40720504 - UCHP-M (2005-2011)
    AV0Z40320502 - UACH-T (2005-2011)
    UT WOS000263922500022
    DOI10.1039/b816790g
    AnnotationA series of diureido-calix[4]arenes immobilised in the 1,3-alternate conformation was synthesised and systematically studied for their complexation ability. As revealed by 1H NMR and UV/vis titrations, this structural motif leads to very efficient ligands for anion recognition with high binding constants in nonpolar solvents. The comparison with the corresponding ligands possessing the cone conformation indicates that diureido-calix[4]arene in a 1,3-alternate conformation are very promising anion receptors with pronounced binding ability towards carboxylates.
    WorkplaceInstitute of Chemical Process Fundamentals
    ContactEva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227
    Year of Publishing2010
Number of the records: 1  

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