Properties of cationic monosubstituted tetraalkylammonium cyclodextrin derivatives ? their stability, complexation ability in solution or when deposited on solid anionic surface
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F15%3A00440651" target="_blank" >RIV/61389013:_____/15:00440651 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11310/15:10295238 RIV/00216208:11320/15:10295238
Výsledek na webu
<a href="http://dx.doi.org/10.3762/bjoc.11.20" target="_blank" >http://dx.doi.org/10.3762/bjoc.11.20</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3762/bjoc.11.20" target="_blank" >10.3762/bjoc.11.20</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Properties of cationic monosubstituted tetraalkylammonium cyclodextrin derivatives ? their stability, complexation ability in solution or when deposited on solid anionic surface
Popis výsledku v původním jazyce
The thermal stability of the monosubstituted cationic cyclodextrin (CD) derivatives PEMEDA-?-CD and PEMPDA-?-CD, which differ in their substituent linker length (ethylene and propylene, respectively), was studied via 1H NMR experiments. PEMPDA-?-CD exhibited higher resistance towards the Hofmann degradation and was chosen as a more suitable host molecule for further studies. Inclusion properties of PEMPDA-?-CD in solution with a series of simple aromatic guests (salicylic acid, p-methoxyphenol and p-nitroaniline) were determined by isothermal titration calorimetry (ITC) and compared to the native ?-CD. Permanently charged cationic CD derivatives were successfully deposited on the anionic solid surface of polymeric Nafion 117 membrane via electrostaticinteractions. Deposition kinetics and coverage of the surface were determined by ELSD. Finally, the ability of the CD derivatives bound to the solid surface to encapsulate aromatic compounds from aqueous solution was measured by UV?vis sp
Název v anglickém jazyce
Properties of cationic monosubstituted tetraalkylammonium cyclodextrin derivatives ? their stability, complexation ability in solution or when deposited on solid anionic surface
Popis výsledku anglicky
The thermal stability of the monosubstituted cationic cyclodextrin (CD) derivatives PEMEDA-?-CD and PEMPDA-?-CD, which differ in their substituent linker length (ethylene and propylene, respectively), was studied via 1H NMR experiments. PEMPDA-?-CD exhibited higher resistance towards the Hofmann degradation and was chosen as a more suitable host molecule for further studies. Inclusion properties of PEMPDA-?-CD in solution with a series of simple aromatic guests (salicylic acid, p-methoxyphenol and p-nitroaniline) were determined by isothermal titration calorimetry (ITC) and compared to the native ?-CD. Permanently charged cationic CD derivatives were successfully deposited on the anionic solid surface of polymeric Nafion 117 membrane via electrostaticinteractions. Deposition kinetics and coverage of the surface were determined by ELSD. Finally, the ability of the CD derivatives bound to the solid surface to encapsulate aromatic compounds from aqueous solution was measured by UV?vis sp
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
CD - Makromolekulární chemie
OECD FORD obor
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Návaznosti výsledku
Projekt
<a href="/cs/project/GAP108%2F12%2F0640" target="_blank" >GAP108/12/0640: Biokompatibilní nanodimantové sondy pro multimodální zobrazování in vivo</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2015
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Beilstein Journal of Organic Chemistry
ISSN
1860-5397
e-ISSN
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Svazek periodika
11
Číslo periodika v rámci svazku
February
Stát vydavatele periodika
DE - Spolková republika Německo
Počet stran výsledku
8
Strana od-do
192-199
Kód UT WoS článku
000349118000001
EID výsledku v databázi Scopus
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