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

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F21%3A10430801" target="_blank" >RIV/00216208:11310/21:10430801 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11320/21:10430801

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=adkDH1wQvZ" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=adkDH1wQvZ</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.mtcomm.2021.102234" target="_blank" >10.1016/j.mtcomm.2021.102234</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

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

  • Original language description

    Three multiply positively charged beta-cyclodextrin derivatives were prepared and ionically bound to a Nafion (R) 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.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10401 - Organic chemistry

Result continuities

  • Project

    <a href="/en/project/FV10082" target="_blank" >FV10082: Novel stationary phases for chromatographic separation of chiral compounds</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2021

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Materials Today Communications [online]

  • ISSN

    2352-4928

  • e-ISSN

  • Volume of the periodical

    27

  • Issue of the periodical within the volume

    June

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    9

  • Pages from-to

    102234

  • UT code for WoS article

    000683034600005

  • EID of the result in the Scopus database

    2-s2.0-85102622535