All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Fast UHPLC enantioseparation of liquid crystalline materials with chiral center based on octanol in reversed-phase and polar organic mode

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378271%3A_____%2F20%3A00560618" target="_blank" >RIV/68378271:_____/20:00560618 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11310/20:10413777

  • Result on the web

    <a href="https://doi.org/10.1007/s00706-020-02622-5" target="_blank" >https://doi.org/10.1007/s00706-020-02622-5</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00706-020-02622-5" target="_blank" >10.1007/s00706-020-02622-5</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Fast UHPLC enantioseparation of liquid crystalline materials with chiral center based on octanol in reversed-phase and polar organic mode

  • Original language description

    Fast baseline enantioseparation of twenty racemic liquid crystalline compounds was carried out via ultra-performance liquid chromatography through direct enantioseparation in polar organic and reversed-phase modes. Tris(3-chloro-5-methylphenylcarbamate) derivative of amylose was used as chiral stationary phase, the chiral selector was covalently mmobilized on sub-2 μm silica particles. Experiments were done using either pure acetonitrile as mobile phase or simple binary mobile phases consisting of acetonitrile/water mixtures. Studied materials are a set of structurally similar compounds comprising two different structures of chiral center, various length of alkoxy spacer and four patterns of lateral substitution of aromatic core by fluorine. The compounds do not contain any ionizable group. The effect of the enantiomer structure on the retention and enantioseparation was evaluated. Flow rate and column temperature were optimized as part of method development.

  • 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/EF16_019%2F0000760" target="_blank" >EF16_019/0000760: Solid State Physics for 21st century</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Monatshefte fur Chemie

  • ISSN

    0026-9247

  • e-ISSN

    1434-4475

  • Volume of the periodical

    151

  • Issue of the periodical within the volume

    8

  • Country of publishing house

    AT - AUSTRIA

  • Number of pages

    6

  • Pages from-to

    1235-1240

  • UT code for WoS article

    000555979300008

  • EID of the result in the Scopus database

    2-s2.0-85085570057