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Use of 6-O-mono-substituted derivatives of β-cyclodextrin-bearing substituent with two permanent positive charges in capillary electrophoresis

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F16%3A10325009" target="_blank" >RIV/00216208:11310/16:10325009 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1515/chempap-2016-0053" target="_blank" >http://dx.doi.org/10.1515/chempap-2016-0053</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1515/chempap-2016-0053" target="_blank" >10.1515/chempap-2016-0053</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Use of 6-O-mono-substituted derivatives of β-cyclodextrin-bearing substituent with two permanent positive charges in capillary electrophoresis

  • Original language description

    This study details the use of two permanently positively charged mono-substituted beta-cyclodextrin derivatives, 6(I)-deoxy-6(I)-(N,N,N',N',N'-pentamethyl-ethylene-1,2-diammonio)-cyclomaltoheptose dichloride (PEMEDA-beta-CD) and the newly synthesised 6(I)-deoxy-6(I)-(N,N,N',N',N'-pentamethylpropylene-1,3-diammonio)-cyclomaltoheptose (PEMPDA-beta-CD) as chiral selectors in capillary electrophoresis. Cyclodextrin (CD) derivatives were tested as additives in various buffers at various pH values with the optional addition of an organic modifier. Fourteen anionogenic analytes were tested, including native amino acids, N-blocked amino acids and profens, which were detected using a UV-VIS detector at optimal wavelengths of 214 nm, 254 nm or 280 nm. A borate buffer (15 mmol L-1) at pH 9.5 without the addition of an organic modifier was chosen as a suitable background electrolyte. In addition, the effect of the concentration of the chiral selector on the separation and enantioseparation of selected analytes was monitored. The additions of cyclodextrin derivatives varied within the concentration range of 0.0-5.0 mmol L-1. Both chiral selectors were suitable for the enantioseparation of N-Boc-D, L-tryptophan, which was already separated on the baseline at 0.5 mmol L-1 concentration of the chiral selector. (c) 2016 Institute of Chemistry, Slovak Academy of Sciences

  • 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/GA13-01440S" target="_blank" >GA13-01440S: Chiral supramolecular polymers based on derivatized cyclodextrins as a new environment for capillary separation techniques</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

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

    Chemical Papers

  • ISSN

    0366-6352

  • e-ISSN

  • Volume of the periodical

    70

  • Issue of the periodical within the volume

    9

  • Country of publishing house

    SK - SLOVAKIA

  • Number of pages

    11

  • Pages from-to

    1144-1154

  • UT code for WoS article

    000378599000002

  • EID of the result in the Scopus database

    2-s2.0-84974555859