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Characterization of new R-naphthylethyl cyclofructan 6 chiral stationary phase and its comparison with R-naphthylethyl beta-cyclodextrin-based column

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F11%3A10089765" target="_blank" >RIV/00216208:11310/11:10089765 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.chroma.2011.01.023" target="_blank" >http://dx.doi.org/10.1016/j.chroma.2011.01.023</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.chroma.2011.01.023" target="_blank" >10.1016/j.chroma.2011.01.023</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Characterization of new R-naphthylethyl cyclofructan 6 chiral stationary phase and its comparison with R-naphthylethyl beta-cyclodextrin-based column

  • Original language description

    Derivatized cyclofructans have been recently introduced as a new class of chiral selectors with great application potential. In this study, a R-naphthylethyl-functionalized cyclofructan 6 based chiral stationary phase (RN CF6 CSP) was used for separationof substituted binaphthyl catalysts in the normal phase HPLC mode. Dominant interaction types that play a role in the separation mechanism were revealed by a linear free energy relationship (LFER) method. In order to evaluate the contribution of the substituent on the cyclofructan structure to retention, the R-naphthylethyl-functionalized beta-cyclodextrin (RN CD) CSP was chosen for comparison. Retention factors of 46 widely different solutes. with known solvation parameters, were determined on each ofthe columns under the same mobile phase compositions used for the enantiomeric separations. The LEER results showed that hydrogen bond acidity and polarity/polarizibility have the greatest impact on retention and enantioresolution on the

  • 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

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2011

  • 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

    1218

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    6

  • Pages from-to

    1393-1398

  • UT code for WoS article

    000288186900010

  • EID of the result in the Scopus database