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Supramolecular structures based on regioisomers of cinnamyl-α-cyclodextrins – new media for capillary separation techniques

This work focuses on the preparation and application of supramolecular structures based on mono-cinnamyl-α-cyclodextrins (Cin-α-CD). Pure regioisomers of Cin-α-CD having the cinnamyl moiety at the 2-O- or at the 3-O-position, respectively, were prepared, characterized and applied in capillary electr...

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Autores principales: Benkovics, Gabor, Hodek, Ondrej, Havlikova, Martina, Bosakova, Zuzana, Coufal, Pavel, Malanga, Milo, Fenyvesi, Eva, Darcsi, Andras, Beni, Szabolcs, Jindrich, Jindrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734354/
https://www.ncbi.nlm.nih.gov/pubmed/26877812
http://dx.doi.org/10.3762/bjoc.12.11
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author Benkovics, Gabor
Hodek, Ondrej
Havlikova, Martina
Bosakova, Zuzana
Coufal, Pavel
Malanga, Milo
Fenyvesi, Eva
Darcsi, Andras
Beni, Szabolcs
Jindrich, Jindrich
author_facet Benkovics, Gabor
Hodek, Ondrej
Havlikova, Martina
Bosakova, Zuzana
Coufal, Pavel
Malanga, Milo
Fenyvesi, Eva
Darcsi, Andras
Beni, Szabolcs
Jindrich, Jindrich
author_sort Benkovics, Gabor
collection PubMed
description This work focuses on the preparation and application of supramolecular structures based on mono-cinnamyl-α-cyclodextrins (Cin-α-CD). Pure regioisomers of Cin-α-CD having the cinnamyl moiety at the 2-O- or at the 3-O-position, respectively, were prepared, characterized and applied in capillary electrophoresis as additives to the background electrolyte. These new monomer units with a potential to self-organize into supramolecular structures were synthesized via a straightforward one-step synthetic procedure and purified using preparative reversed-phase chromatography allowing a large scale separation of the regioisomers. The ability of the monomers to self-assemble was proved by various methods including NMR spectroscopy and dynamic light scattering (DLS). The light scattering experiments showed that the monomer units have distinguishable ability to form supramolecular structures in different solvents and the size distribution of the aggregates in water can be easily modulated using different external stimuli, such as temperature or competitive guest molecules. The obtained results indicated that the two regioisomers of Cin-α-CD formed different supramolecular assemblies highlighting the fact that the position of the cinnamyl group plays an important role in the intermolecular complex formation.
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spelling pubmed-47343542016-02-12 Supramolecular structures based on regioisomers of cinnamyl-α-cyclodextrins – new media for capillary separation techniques Benkovics, Gabor Hodek, Ondrej Havlikova, Martina Bosakova, Zuzana Coufal, Pavel Malanga, Milo Fenyvesi, Eva Darcsi, Andras Beni, Szabolcs Jindrich, Jindrich Beilstein J Org Chem Full Research Paper This work focuses on the preparation and application of supramolecular structures based on mono-cinnamyl-α-cyclodextrins (Cin-α-CD). Pure regioisomers of Cin-α-CD having the cinnamyl moiety at the 2-O- or at the 3-O-position, respectively, were prepared, characterized and applied in capillary electrophoresis as additives to the background electrolyte. These new monomer units with a potential to self-organize into supramolecular structures were synthesized via a straightforward one-step synthetic procedure and purified using preparative reversed-phase chromatography allowing a large scale separation of the regioisomers. The ability of the monomers to self-assemble was proved by various methods including NMR spectroscopy and dynamic light scattering (DLS). The light scattering experiments showed that the monomer units have distinguishable ability to form supramolecular structures in different solvents and the size distribution of the aggregates in water can be easily modulated using different external stimuli, such as temperature or competitive guest molecules. The obtained results indicated that the two regioisomers of Cin-α-CD formed different supramolecular assemblies highlighting the fact that the position of the cinnamyl group plays an important role in the intermolecular complex formation. Beilstein-Institut 2016-01-19 /pmc/articles/PMC4734354/ /pubmed/26877812 http://dx.doi.org/10.3762/bjoc.12.11 Text en Copyright © 2016, Benkovics et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Benkovics, Gabor
Hodek, Ondrej
Havlikova, Martina
Bosakova, Zuzana
Coufal, Pavel
Malanga, Milo
Fenyvesi, Eva
Darcsi, Andras
Beni, Szabolcs
Jindrich, Jindrich
Supramolecular structures based on regioisomers of cinnamyl-α-cyclodextrins – new media for capillary separation techniques
title Supramolecular structures based on regioisomers of cinnamyl-α-cyclodextrins – new media for capillary separation techniques
title_full Supramolecular structures based on regioisomers of cinnamyl-α-cyclodextrins – new media for capillary separation techniques
title_fullStr Supramolecular structures based on regioisomers of cinnamyl-α-cyclodextrins – new media for capillary separation techniques
title_full_unstemmed Supramolecular structures based on regioisomers of cinnamyl-α-cyclodextrins – new media for capillary separation techniques
title_short Supramolecular structures based on regioisomers of cinnamyl-α-cyclodextrins – new media for capillary separation techniques
title_sort supramolecular structures based on regioisomers of cinnamyl-α-cyclodextrins – new media for capillary separation techniques
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734354/
https://www.ncbi.nlm.nih.gov/pubmed/26877812
http://dx.doi.org/10.3762/bjoc.12.11
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