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Chiral separation of novel diazenes on a polysaccharide-basedstationary phase in the reversed-phase mode

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    SYSNO ASEP0483337
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleChiral separation of novel diazenes on a polysaccharide-basedstationary phase in the reversed-phase mode
    Author(s) Vojtylová, Terézia (FZU-D)
    Hamplová, Věra (FZU-D) RID, ORCID, SAI
    Galewski, Z. (PL)
    Korbecka, I. (PL)
    Sýkora, D. (CZ)
    Number of authors5
    Source TitleJournal of Separation Science. - : Wiley - ISSN 1615-9306
    Roč. 40, č. 7 (2017), s. 1465-1469
    Number of pages5 s.
    Publication formPrint - P
    Languageeng - English
    CountryDE - Germany
    Keywordsazobenzene ; chiral separation ; high-performance liquid chromatography ; liquid-crystalline materials ; photo-induced isomerization
    Subject RIVCB - Analytical Chemistry, Separation
    OECD categoryAnalytical chemistry
    R&D ProjectsGA15-02843S GA ČR - Czech Science Foundation (CSF)
    Institutional supportFZU-D - RVO:68378271
    UT WOS000399782900004
    EID SCOPUS85016956613
    DOI10.1002/jssc.201601386
    AnnotationChiral HPLC separation of two recently synthesized liquid crystalline materials C1 and C2 was studied in the reversed-phase mode. Both materials have an azo-moiety and one chiral center in their molecular structures. The compounds were analyzed in both of their possible forms, the more thermodynamically stable E form and the labile Z form. The conditions and time scale of the UV-induced E toZ transition were briefly evaluated. Under the optimized conditions, we were able to baseline separate S and R enantiomers of both of the studied materials not only in their E forms, but also in their Z forms. In comparison to the separation in the normal-phase mode, which we have reported recently, the resolution in the reversed-phase mode is significantly better. Interestingly, peak reversal was noticed for the S and R enantiomers when the separation was carried out with E versus Z forms of both compounds.
    WorkplaceInstitute of Physics
    ContactKristina Potocká, potocka@fzu.cz, Tel.: 220 318 579
    Year of Publishing2018
Number of the records: 1  

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