Imidazolium Based Multitopic Guest with 1,3-Adamantylene Centerpiece
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70883521%3A28110%2F14%3A43871675" target="_blank" >RIV/70883521:28110/14:43871675 - isvavai.cz</a>
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Imidazolium Based Multitopic Guest with 1,3-Adamantylene Centerpiece
Popis výsledku v původním jazyce
Supramolecular host-guest systems involving adamantane derivatives as building units or regulators of an aggregation process have been extensively studied. As adamantane is a lipophilic and round-shaped hydrocarbon, its derivatives fit precisely the interior cavity of b-cyclodextrin (b-CD) and cucurbit[7]uril (CB7) to form water-soluble, highly stable inclusion complexes with the association constants up to 106 m-1 and 1015 m-1, respectively. Accordingly, we designed a novel multitopic guest molecules based on bisimidazolium salts with 1,3-adamantylene centerpiece. Commercial 1,3-adamantanediacetic acid was transformed via sequential esterification, reduction, Appel reaction and quarternization to produce three final guests 1?3 as depicted in Scheme 1.The binding ability of prepared ligands towards b-CD, g-CD, CB7 and CB8, was studied in water solution using NMR and titration calorimetry and in the gas phase using ESI-MS.
Název v anglickém jazyce
Imidazolium Based Multitopic Guest with 1,3-Adamantylene Centerpiece
Popis výsledku anglicky
Supramolecular host-guest systems involving adamantane derivatives as building units or regulators of an aggregation process have been extensively studied. As adamantane is a lipophilic and round-shaped hydrocarbon, its derivatives fit precisely the interior cavity of b-cyclodextrin (b-CD) and cucurbit[7]uril (CB7) to form water-soluble, highly stable inclusion complexes with the association constants up to 106 m-1 and 1015 m-1, respectively. Accordingly, we designed a novel multitopic guest molecules based on bisimidazolium salts with 1,3-adamantylene centerpiece. Commercial 1,3-adamantanediacetic acid was transformed via sequential esterification, reduction, Appel reaction and quarternization to produce three final guests 1?3 as depicted in Scheme 1.The binding ability of prepared ligands towards b-CD, g-CD, CB7 and CB8, was studied in water solution using NMR and titration calorimetry and in the gas phase using ESI-MS.
Klasifikace
Druh
O - Ostatní výsledky
CEP obor
CC - Organická chemie
OECD FORD obor
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Návaznosti výsledku
Projekt
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Návaznosti
S - Specificky vyzkum na vysokych skolach
Ostatní
Rok uplatnění
2014
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů