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Soccer goes BOXing: Synthetic access to novel [6:0] hexakis[(bisoxazolinyl)methano]fullerenes

The syntheses of [6:0] hexakis[(bisoxazolinyl)methano]fullerenes are presented. Two derivatives could be directly obtained using conditions developed by the Sun group. For the remaining products, a two stage protocol had to be developed. All compounds we obtained in synthetically useful scales and w...

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Autores principales: Seifermann, Stefan M., Réthoré, Céline, Muller, Thierry, Bräse, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3788375/
https://www.ncbi.nlm.nih.gov/pubmed/24085228
http://dx.doi.org/10.1038/srep02817
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author Seifermann, Stefan M.
Réthoré, Céline
Muller, Thierry
Bräse, Stefan
author_facet Seifermann, Stefan M.
Réthoré, Céline
Muller, Thierry
Bräse, Stefan
author_sort Seifermann, Stefan M.
collection PubMed
description The syntheses of [6:0] hexakis[(bisoxazolinyl)methano]fullerenes are presented. Two derivatives could be directly obtained using conditions developed by the Sun group. For the remaining products, a two stage protocol had to be developed. All compounds we obtained in synthetically useful scales and were purified via column chromatography with standard achiral phase. These new fullerene adducts bear six metal-chelation sites which are aligned in the three orthogonal space directions and are disposed on a completely rigid scaffold. First experiments indicate that the generation of six-fold metal-complexes is possible with these structures. This makes them very appealing as ligands in asymmetric catalysis and as building blocks in higher supra-molecular assemblies.
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spelling pubmed-37883752013-10-18 Soccer goes BOXing: Synthetic access to novel [6:0] hexakis[(bisoxazolinyl)methano]fullerenes Seifermann, Stefan M. Réthoré, Céline Muller, Thierry Bräse, Stefan Sci Rep Article The syntheses of [6:0] hexakis[(bisoxazolinyl)methano]fullerenes are presented. Two derivatives could be directly obtained using conditions developed by the Sun group. For the remaining products, a two stage protocol had to be developed. All compounds we obtained in synthetically useful scales and were purified via column chromatography with standard achiral phase. These new fullerene adducts bear six metal-chelation sites which are aligned in the three orthogonal space directions and are disposed on a completely rigid scaffold. First experiments indicate that the generation of six-fold metal-complexes is possible with these structures. This makes them very appealing as ligands in asymmetric catalysis and as building blocks in higher supra-molecular assemblies. Nature Publishing Group 2013-10-02 /pmc/articles/PMC3788375/ /pubmed/24085228 http://dx.doi.org/10.1038/srep02817 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Article
Seifermann, Stefan M.
Réthoré, Céline
Muller, Thierry
Bräse, Stefan
Soccer goes BOXing: Synthetic access to novel [6:0] hexakis[(bisoxazolinyl)methano]fullerenes
title Soccer goes BOXing: Synthetic access to novel [6:0] hexakis[(bisoxazolinyl)methano]fullerenes
title_full Soccer goes BOXing: Synthetic access to novel [6:0] hexakis[(bisoxazolinyl)methano]fullerenes
title_fullStr Soccer goes BOXing: Synthetic access to novel [6:0] hexakis[(bisoxazolinyl)methano]fullerenes
title_full_unstemmed Soccer goes BOXing: Synthetic access to novel [6:0] hexakis[(bisoxazolinyl)methano]fullerenes
title_short Soccer goes BOXing: Synthetic access to novel [6:0] hexakis[(bisoxazolinyl)methano]fullerenes
title_sort soccer goes boxing: synthetic access to novel [6:0] hexakis[(bisoxazolinyl)methano]fullerenes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3788375/
https://www.ncbi.nlm.nih.gov/pubmed/24085228
http://dx.doi.org/10.1038/srep02817
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