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Advantages of polar organic solvent chromatography for enantioseparation of chiral liquid crystals

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378271%3A_____%2F23%3A00580266" target="_blank" >RIV/68378271:_____/23:00580266 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11310/23:10470994

  • Result on the web

    <a href="https://doi.org/10.1016/j.chroma.2023.464383" target="_blank" >https://doi.org/10.1016/j.chroma.2023.464383</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.chroma.2023.464383" target="_blank" >10.1016/j.chroma.2023.464383</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Advantages of polar organic solvent chromatography for enantioseparation of chiral liquid crystals

  • Original language description

    Three sets of fluorinated chiral liquid crystals were used to explore the polar organic solvent chromatography mode for their enantioseparation. The materials include a set of newly synthesized compounds with chiral center derived from 2-hexanol and two sets of compounds with chiral center derived from 2-/3-octanol. Baseline enantioseparation of all materials was achieved using binary mobile phases without additives.The mobile phases tested included whole range of acetonitrile/methanol mixtures to demonstrate that acetonitrile-rich and alcohol-rich mobile phases offer different enantiorecognition mechanisms and can provide complementarity to some extent. The effect of temperature on enantioseparation was investigated on Chiralpak IA-U by constructing van’t Hoff plots for selected liquid crystals in pure acetonitrile and pure methanol as mobile phases.

  • 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

    10406 - Analytical chemistry

Result continuities

  • Project

    <a href="/en/project/GA22-16499S" target="_blank" >GA22-16499S: Chirality as a tool for controlling photoresponsiveness of supramolecular arrangements</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Chromatography A

  • ISSN

    0021-9673

  • e-ISSN

    1873-3778

  • Volume of the periodical

    1709

  • Issue of the periodical within the volume

    Oct

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    7

  • Pages from-to

    464383

  • UT code for WoS article

    001079632700001

  • EID of the result in the Scopus database

    2-s2.0-85171367373