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Chiral HPLC and physical characterisation of orthoconic antiferroelectric liquid crystals

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22340%2F16%3A43901616" target="_blank" >RIV/60461373:22340/16:43901616 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378271:_____/16:00468708

  • Result on the web

    <a href="http://dx.doi.org/10.1080/02678292.2016.1166401" target="_blank" >http://dx.doi.org/10.1080/02678292.2016.1166401</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1080/02678292.2016.1166401" target="_blank" >10.1080/02678292.2016.1166401</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Chiral HPLC and physical characterisation of orthoconic antiferroelectric liquid crystals

  • Original language description

    New orthoconic antiferroelectric liquid crystalline materials were synthesised and characterised in their racemic forms and as (S) enantiomers. The materials possess oligo-methylene spacers of different lengths in semi-fluorinated achiral chains and lateral substitution by fluorine at two different positions of the molecular core. For comparison purposes, analogical materials without fluorine lateral substitutions were also prepared. Polysaccharide chiral stationary phases based on two different chiral selectors were used for the separation of the enantiomers of the individual racemic mixtures by high-performance liquid chromatography. A baseline separation of (S) and (R) enantiomers was obtained for four of the six studied liquid crystalline materials. Two of the materials were partially separated under the optimised separation conditions. The elution order of the individual enantiomers in the racemic mixtures was successfully assigned, as pure (S) enantiomers of all the studied materials were available. Both the position of the fluorine atom within the molecular core and the size of the achiral moiety had significant effects on the separation of the individual enantiomers of the studied compounds. Moreover, it was also found that the structure of the chiral stationary phase selector significantly influenced the enantiomeric resolution.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CB - Analytical chemistry, separation

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2016

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Liquid Crystals

  • ISSN

    0267-8292

  • e-ISSN

  • Volume of the periodical

    43

  • Issue of the periodical within the volume

    9

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    7

  • Pages from-to

    1244-1250

  • UT code for WoS article

    000378082500011

  • EID of the result in the Scopus database

    2-s2.0-84962106309