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Chiral Nafion membranes prepared by strong electrostatic binding of multiply positively charged β-cyclodextrin derivatives for tryptophan racemic mixtures’ separation.

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    SYSNO ASEP0541140
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleChiral Nafion membranes prepared by strong electrostatic binding of multiply positively charged β-cyclodextrin derivatives for tryptophan racemic mixtures’ separation.
    Author(s) Kasal, P. (CZ)
    Michel, Marine (UCHP-M)
    Gaálová, Jana (UCHP-M) RID, SAI, ORCID
    Cuřínová, Petra (UCHP-M) RID, SAI, ORCID
    Izák, Pavel (UCHP-M) RID, ORCID, SAI
    Jindřich, J. (CZ)
    Article number102234
    Source TitleMaterials Today Communications. - : Elsevier - ISSN 2352-4928
    Roč. 27, JUN 2021 (2021)
    Number of pages9 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordsoptical resolution ; cyclodextrins ; racemic mixtures
    Subject RIVCI - Industrial Chemistry, Chemical Engineering
    OECD categoryChemical process engineering
    R&D ProjectsGA20-09980S GA ČR - Czech Science Foundation (CSF)
    FV10082 GA MPO - Ministry of Industry and Trade (MPO)
    Method of publishingOpen access with time embargo (01.07.2023)
    Institutional supportUCHP-M - RVO:67985858
    UT WOS000683034600005
    EID SCOPUS85102622535
    DOI10.1016/j.mtcomm.2021.102234
    AnnotationThree multiply positively charged β-cyclodextrin derivatives were prepared and ionically bound to a Nafion® 117 membrane. The derivatives differed only in the length of the linker, which connects the positively charged anchor to the cyclodextrin moiety. The resulting membranes exert preferential sorption of l-enantiomer of tryptophan from its racemic mixture (ee reaching 44 % for the medium linker length). The membrane follows the retarded transport mechanism. Using a fluorophore-tagged cyclodextrin modifier, we confirmed no leaching of the modifier from the membrane. Thus, we proved the potential of the approach of electrostatic binding of chiral selectors for the enantioseparation of chiral drugs.
    WorkplaceInstitute of Chemical Process Fundamentals
    ContactEva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227
    Year of Publishing2022
    Electronic addresshttp://hdl.handle.net/11104/0318741
Number of the records: 1  

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