Cyclodextrins as Chiral Selectors in Capillary Electrophoresis Enantioseparations

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11160%2F19%3A10400759" target="_blank" >RIV/00216208:11160/19:10400759 - isvavai.cz</a>
Result on the web
<a href="http://link.springer.com/protocol/10.1007/978-1-4939-9438-0_18" target="_blank" >http://link.springer.com/protocol/10.1007/978-1-4939-9438-0_18</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/978-1-4939-9438-0_18" target="_blank" >10.1007/978-1-4939-9438-0_18</a>

Result language
angličtina
Original language name
Cyclodextrins as Chiral Selectors in Capillary Electrophoresis Enantioseparations
Original language description
Due to their structural variability and their commercial availability, cyclodextrins are the most frequently used chiral selectors in capillary electrophoresis. A variety of migration modes can be realized depending on the characteristics of the cyclodextrins and the analytes. The basic considerations regarding the development of a chiral CE method employing cyclodextrins as chiral selectors are briefly discussed. The presented examples illustrate the separation modes of an acidic and a basic analyte with native and charged cyclodextrin derivatives as a function of the pH of the background electrolyte and the concentration of the cyclodextrin.
Czech name
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Czech description
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Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2019
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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