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Supramolecular chemistry: from aromatic foldamers to solution-phase supramolecular organic frameworks
This mini-review covers the growth, education, career, and research activities of the author. In particular, the developments of various folded, helical and extended secondary structures from aromatic backbones driven by different noncovalent forces (including hydrogen bonding, donor–acceptor, solvo...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661011/ https://www.ncbi.nlm.nih.gov/pubmed/26664626 http://dx.doi.org/10.3762/bjoc.11.222 |
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author | Li, Zhan-Ting |
author_facet | Li, Zhan-Ting |
author_sort | Li, Zhan-Ting |
collection | PubMed |
description | This mini-review covers the growth, education, career, and research activities of the author. In particular, the developments of various folded, helical and extended secondary structures from aromatic backbones driven by different noncovalent forces (including hydrogen bonding, donor–acceptor, solvophobicity, and dimerization of conjugated radical cations) and solution-phase supramolecular organic frameworks driven by hydrophobically initiated aromatic stacking in the cavity of cucurbit[8]uril (CB[8]) are highlighted. |
format | Online Article Text |
id | pubmed-4661011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-46610112015-12-09 Supramolecular chemistry: from aromatic foldamers to solution-phase supramolecular organic frameworks Li, Zhan-Ting Beilstein J Org Chem Review This mini-review covers the growth, education, career, and research activities of the author. In particular, the developments of various folded, helical and extended secondary structures from aromatic backbones driven by different noncovalent forces (including hydrogen bonding, donor–acceptor, solvophobicity, and dimerization of conjugated radical cations) and solution-phase supramolecular organic frameworks driven by hydrophobically initiated aromatic stacking in the cavity of cucurbit[8]uril (CB[8]) are highlighted. Beilstein-Institut 2015-11-02 /pmc/articles/PMC4661011/ /pubmed/26664626 http://dx.doi.org/10.3762/bjoc.11.222 Text en Copyright © 2015, Li 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 | Review Li, Zhan-Ting Supramolecular chemistry: from aromatic foldamers to solution-phase supramolecular organic frameworks |
title | Supramolecular chemistry: from aromatic foldamers to solution-phase supramolecular organic frameworks |
title_full | Supramolecular chemistry: from aromatic foldamers to solution-phase supramolecular organic frameworks |
title_fullStr | Supramolecular chemistry: from aromatic foldamers to solution-phase supramolecular organic frameworks |
title_full_unstemmed | Supramolecular chemistry: from aromatic foldamers to solution-phase supramolecular organic frameworks |
title_short | Supramolecular chemistry: from aromatic foldamers to solution-phase supramolecular organic frameworks |
title_sort | supramolecular chemistry: from aromatic foldamers to solution-phase supramolecular organic frameworks |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661011/ https://www.ncbi.nlm.nih.gov/pubmed/26664626 http://dx.doi.org/10.3762/bjoc.11.222 |
work_keys_str_mv | AT lizhanting supramolecularchemistryfromaromaticfoldamerstosolutionphasesupramolecularorganicframeworks |