Synthesis and supramolecular properties of glycoluril tetramer

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F14%3A00073515" target="_blank" >RIV/00216224:14310/14:00073515 - isvavai.cz</a>
Result on the web
<a href="http://www.tandfonline.com/doi/abs/10.1080/10610278.2013.842643" target="_blank" >http://www.tandfonline.com/doi/abs/10.1080/10610278.2013.842643</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1080/10610278.2013.842643" target="_blank" >10.1080/10610278.2013.842643</a>

Result language
angličtina
Original language name
Synthesis and supramolecular properties of glycoluril tetramer
Original language description
We have synthesised a tetramer as a new host molecule based on glycoluril. We have demonstrated the ability of it to undergo dimerisation in the solid state. The host?guest properties in the solution have been investigated using 1H NMR spectrometry. It has been found that the tetramer binds organic guests in the same preferences as CB6 although absolute binding constants are about one order of magnitude lower. Different binding properties of tetramer and previously reported derivate indicate that the attachment of functional groups to the terminal units of tetramer can significantly affect the binding affinity and, moreover, selectivity of these acyclic oligomers.
Czech name
—
Czech description
—

Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—

Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2014
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Similar results(10)