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Novel supramolecular affinity materials based on (−)-isosteviol as molecular templates
The readily available ex-chiral-pool building block (−)-isosteviol was combined with the C(3)-symmetric platforms hexahydroxytriphenylene and hexaaminotriptycene providing large and rigid molecular architectures. Because of the persistent cavities these scaffolds are very potent supramolecular affin...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869372/ https://www.ncbi.nlm.nih.gov/pubmed/24367446 http://dx.doi.org/10.3762/bjoc.9.317 |
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author | Lohoelter, Christina Brutschy, Malte Lubczyk, Daniel Waldvogel, Siegfried R |
author_facet | Lohoelter, Christina Brutschy, Malte Lubczyk, Daniel Waldvogel, Siegfried R |
author_sort | Lohoelter, Christina |
collection | PubMed |
description | The readily available ex-chiral-pool building block (−)-isosteviol was combined with the C(3)-symmetric platforms hexahydroxytriphenylene and hexaaminotriptycene providing large and rigid molecular architectures. Because of the persistent cavities these scaffolds are very potent supramolecular affinity materials for head space analysis by quartz crystal microbalances. The scaffolds serve in particular as templates for tracing air-borne arenes at low concentration. The affinities of the synthesized materials towards different air-borne arenes were determined by 200 MHz quartz crystal microbalances. |
format | Online Article Text |
id | pubmed-3869372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-38693722013-12-23 Novel supramolecular affinity materials based on (−)-isosteviol as molecular templates Lohoelter, Christina Brutschy, Malte Lubczyk, Daniel Waldvogel, Siegfried R Beilstein J Org Chem Full Research Paper The readily available ex-chiral-pool building block (−)-isosteviol was combined with the C(3)-symmetric platforms hexahydroxytriphenylene and hexaaminotriptycene providing large and rigid molecular architectures. Because of the persistent cavities these scaffolds are very potent supramolecular affinity materials for head space analysis by quartz crystal microbalances. The scaffolds serve in particular as templates for tracing air-borne arenes at low concentration. The affinities of the synthesized materials towards different air-borne arenes were determined by 200 MHz quartz crystal microbalances. Beilstein-Institut 2013-12-09 /pmc/articles/PMC3869372/ /pubmed/24367446 http://dx.doi.org/10.3762/bjoc.9.317 Text en Copyright © 2013, Lohoelter 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 Lohoelter, Christina Brutschy, Malte Lubczyk, Daniel Waldvogel, Siegfried R Novel supramolecular affinity materials based on (−)-isosteviol as molecular templates |
title | Novel supramolecular affinity materials based on (−)-isosteviol as molecular templates |
title_full | Novel supramolecular affinity materials based on (−)-isosteviol as molecular templates |
title_fullStr | Novel supramolecular affinity materials based on (−)-isosteviol as molecular templates |
title_full_unstemmed | Novel supramolecular affinity materials based on (−)-isosteviol as molecular templates |
title_short | Novel supramolecular affinity materials based on (−)-isosteviol as molecular templates |
title_sort | novel supramolecular affinity materials based on (−)-isosteviol as molecular templates |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869372/ https://www.ncbi.nlm.nih.gov/pubmed/24367446 http://dx.doi.org/10.3762/bjoc.9.317 |
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