- Properties of cationic monosubstituted tetraalkylammonium cyclodextri…
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Properties of cationic monosubstituted tetraalkylammonium cyclodextrin derivatives – their stability, complexation ability in solution or when deposited on solid anionic surface

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    SYSNO ASEP0440651
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleProperties of cationic monosubstituted tetraalkylammonium cyclodextrin derivatives – their stability, complexation ability in solution or when deposited on solid anionic surface
    Author(s) Popr, M. (CZ)
    Filippov, Sergey K. (UMCH-V) RID, ORCID, SAI
    Matushkin, Nikolai (UMCH-V)
    Dian, J. (CZ)
    Jindřich, J. (CZ)
    Source TitleBeilstein Journal of Organic Chemistry. - : Beilstein - Institut zur Foerderung der Chemischen Wissenschaften - ISSN 1860-5397
    Roč. 11, February (2015), s. 192-199
    Number of pages8 s.
    Languageeng - English
    CountryDE - Germany
    Keywordscyclodextrins ; inclusion properties ; solid surface
    Subject RIVCD - Macromolecular Chemistry
    R&D ProjectsGAP108/12/0640 GA ČR - Czech Science Foundation (CSF)
    Institutional supportUMCH-V - RVO:61389013
    UT WOS000349118000001
    EID SCOPUS84922196411
    DOI https://doi.org/10.3762/bjoc.11.20
    AnnotationThe thermal stability of the monosubstituted cationic cyclodextrin (CD) derivatives PEMEDA-β-CD and PEMPDA-β-CD, which differ in their substituent linker length (ethylene and propylene, respectively), was studied via 1H NMR experiments. PEMPDA-β-CD exhibited higher resistance towards the Hofmann degradation and was chosen as a more suitable host molecule for further studies. Inclusion properties of PEMPDA-β-CD in solution with a series of simple aromatic guests (salicylic acid, p-methoxyphenol and p-nitroaniline) were determined by isothermal titration calorimetry (ITC) and compared to the native β-CD. Permanently charged cationic CD derivatives were successfully deposited on the anionic solid surface of polymeric Nafion® 117 membrane via electrostatic interactions. Deposition kinetics and coverage of the surface were determined by ELSD. Finally, the ability of the CD derivatives bound to the solid surface to encapsulate aromatic compounds from aqueous solution was measured by UV–vis spectroscopy. The obtained results are promising for future industrial applications of the monosubstituted β-CD derivatives, because the preparation of cationic CD derivatives is applicable in large scale, without the need of chromatographic purification. Their ionic deposition on a solid surface is simple, yet robust and a straightforward process as well.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2015
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