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
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CB - Analytical chemistry, separation
OECD FORD branch
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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
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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