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Isopropyl derivative of cyclofructan 6 as chiral selector in liquid chromatography and capillary electrophoresis

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F14%3A10210823" target="_blank" >RIV/00216208:11310/14:10210823 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15310/14:33151624

  • Result on the web

    <a href="http://ac.els-cdn.com/S0021967314003082/1-s2.0-S0021967314003082-main.pdf?_tid=4b7d2aa8-a565-11e4-9f63-00000aab0f27&acdnat=1422281700_ba51d203583eb9c739089a75bba077dd" target="_blank" >http://ac.els-cdn.com/S0021967314003082/1-s2.0-S0021967314003082-main.pdf?_tid=4b7d2aa8-a565-11e4-9f63-00000aab0f27&acdnat=1422281700_ba51d203583eb9c739089a75bba077dd</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.chroma.2014.02.061" target="_blank" >10.1016/j.chroma.2014.02.061</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Isopropyl derivative of cyclofructan 6 as chiral selector in liquid chromatography and capillary electrophoresis

  • Original language description

    Cyclofructans and preferentially their derivatives can serve as chiral selectors for the separation of different enantiomers/atropisomers. Moreover, the strong ionophoric nature of the 18-crown-6 ether core of cyclofructan 6 for barium cations may be exploited to enhance or modify enantioselectivity. In this work isopropyl-cyclofructan-6 was used as a chiral selector for the separation of binaphthyl atropisomers in HPLC and CE. The data from both separation systems were compared with each other. While in HPLC the chiral selector was bonded to silica gel to afford a chiral stationary phase, in capillary electrophoresis it was reely mobile n the background electrolytes (BGE). This significant difference is reflected in the separation potential of the twoseparation systems. All five analytes could be baseline separated in HPLC (reversed phase mode) while only one derivative was baseline resolved in CE. This result was attributed to the more rigid nature of the immobilized chiral selector

  • 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

    <a href="/en/project/LH11018" target="_blank" >LH11018: Cyclofructans and their derivatives as new chiral selectors for liquid chromatography and capillary electrophoresis</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2014

  • 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

  • Volume of the periodical

    1338

  • Issue of the periodical within the volume

    APRIL 18

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    4

  • Pages from-to

    197-200

  • UT code for WoS article

    000334137200023

  • EID of the result in the Scopus database