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Reversible mechanical protection: building a 3D “suit” around a T-shaped benzimidazole axle

The T-shaped benzimidazolium/crown ether recognition motif was used to prepare suit[1]anes. These novel mechanically interlocked molecules (MIMs) were fully characterized by (1)H and (13)C NMR spectroscopy, single-crystal X-ray diffraction, UV-vis absorption and fluorescence spectroscopy. By convers...

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Detalles Bibliográficos
Autores principales: Zhu, Kelong, Baggi, Giorgio, Vukotic, V. Nicholas, Loeb, Stephen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465563/
https://www.ncbi.nlm.nih.gov/pubmed/28626559
http://dx.doi.org/10.1039/c7sc00790f
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author Zhu, Kelong
Baggi, Giorgio
Vukotic, V. Nicholas
Loeb, Stephen J.
author_facet Zhu, Kelong
Baggi, Giorgio
Vukotic, V. Nicholas
Loeb, Stephen J.
author_sort Zhu, Kelong
collection PubMed
description The T-shaped benzimidazolium/crown ether recognition motif was used to prepare suit[1]anes. These novel mechanically interlocked molecules (MIMs) were fully characterized by (1)H and (13)C NMR spectroscopy, single-crystal X-ray diffraction, UV-vis absorption and fluorescence spectroscopy. By conversion to a suit[1]ane, a simple benzimidazole was shown to be protected from deprotonation by strong base. Moreover, it was demonstrated that this unique three-dimensional encapsulation can be made reversible, thus introducing the concept of “reversible mechanical protection”; a protecting methodology that may have potential applications in synthetic organic chemistry and the design of molecular machinery.
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spelling pubmed-54655632017-06-16 Reversible mechanical protection: building a 3D “suit” around a T-shaped benzimidazole axle Zhu, Kelong Baggi, Giorgio Vukotic, V. Nicholas Loeb, Stephen J. Chem Sci Chemistry The T-shaped benzimidazolium/crown ether recognition motif was used to prepare suit[1]anes. These novel mechanically interlocked molecules (MIMs) were fully characterized by (1)H and (13)C NMR spectroscopy, single-crystal X-ray diffraction, UV-vis absorption and fluorescence spectroscopy. By conversion to a suit[1]ane, a simple benzimidazole was shown to be protected from deprotonation by strong base. Moreover, it was demonstrated that this unique three-dimensional encapsulation can be made reversible, thus introducing the concept of “reversible mechanical protection”; a protecting methodology that may have potential applications in synthetic organic chemistry and the design of molecular machinery. Royal Society of Chemistry 2017-05-01 2017-03-28 /pmc/articles/PMC5465563/ /pubmed/28626559 http://dx.doi.org/10.1039/c7sc00790f Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Zhu, Kelong
Baggi, Giorgio
Vukotic, V. Nicholas
Loeb, Stephen J.
Reversible mechanical protection: building a 3D “suit” around a T-shaped benzimidazole axle
title Reversible mechanical protection: building a 3D “suit” around a T-shaped benzimidazole axle
title_full Reversible mechanical protection: building a 3D “suit” around a T-shaped benzimidazole axle
title_fullStr Reversible mechanical protection: building a 3D “suit” around a T-shaped benzimidazole axle
title_full_unstemmed Reversible mechanical protection: building a 3D “suit” around a T-shaped benzimidazole axle
title_short Reversible mechanical protection: building a 3D “suit” around a T-shaped benzimidazole axle
title_sort reversible mechanical protection: building a 3d “suit” around a t-shaped benzimidazole axle
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465563/
https://www.ncbi.nlm.nih.gov/pubmed/28626559
http://dx.doi.org/10.1039/c7sc00790f
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