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Tuning the size of a redox-active tetrathiafulvalene-based self-assembled ring
The synthesis of a new Pd coordination-driven self-assembled ring M(6)L(3) constructed from a concave tetrapyridyl π-extended tetrathiafulvalene ligand (exTTF) is described. The same ligand is also able to self-assemble in a M(4)L(2) mode as previously described. Herein, we demonstrate that the bulk...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464414/ https://www.ncbi.nlm.nih.gov/pubmed/26124899 http://dx.doi.org/10.3762/bjoc.11.108 |
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author | Bivaud, Sébastien Goeb, Sébastien Croué, Vincent Allain, Magali Pop, Flavia Sallé, Marc |
author_facet | Bivaud, Sébastien Goeb, Sébastien Croué, Vincent Allain, Magali Pop, Flavia Sallé, Marc |
author_sort | Bivaud, Sébastien |
collection | PubMed |
description | The synthesis of a new Pd coordination-driven self-assembled ring M(6)L(3) constructed from a concave tetrapyridyl π-extended tetrathiafulvalene ligand (exTTF) is described. The same ligand is also able to self-assemble in a M(4)L(2) mode as previously described. Herein, we demonstrate that the bulkiness of the ancillary groups in the Pd complex allows for modulating the size and the shape of the resulting discrete self-assembly, which therefore incorporate two (M(4)L(2)) or three (M(6)L(3)) electroactive exTTF sidewalls. |
format | Online Article Text |
id | pubmed-4464414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-44644142015-06-29 Tuning the size of a redox-active tetrathiafulvalene-based self-assembled ring Bivaud, Sébastien Goeb, Sébastien Croué, Vincent Allain, Magali Pop, Flavia Sallé, Marc Beilstein J Org Chem Letter The synthesis of a new Pd coordination-driven self-assembled ring M(6)L(3) constructed from a concave tetrapyridyl π-extended tetrathiafulvalene ligand (exTTF) is described. The same ligand is also able to self-assemble in a M(4)L(2) mode as previously described. Herein, we demonstrate that the bulkiness of the ancillary groups in the Pd complex allows for modulating the size and the shape of the resulting discrete self-assembly, which therefore incorporate two (M(4)L(2)) or three (M(6)L(3)) electroactive exTTF sidewalls. Beilstein-Institut 2015-06-05 /pmc/articles/PMC4464414/ /pubmed/26124899 http://dx.doi.org/10.3762/bjoc.11.108 Text en Copyright © 2015, Bivaud 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 | Letter Bivaud, Sébastien Goeb, Sébastien Croué, Vincent Allain, Magali Pop, Flavia Sallé, Marc Tuning the size of a redox-active tetrathiafulvalene-based self-assembled ring |
title | Tuning the size of a redox-active tetrathiafulvalene-based self-assembled ring |
title_full | Tuning the size of a redox-active tetrathiafulvalene-based self-assembled ring |
title_fullStr | Tuning the size of a redox-active tetrathiafulvalene-based self-assembled ring |
title_full_unstemmed | Tuning the size of a redox-active tetrathiafulvalene-based self-assembled ring |
title_short | Tuning the size of a redox-active tetrathiafulvalene-based self-assembled ring |
title_sort | tuning the size of a redox-active tetrathiafulvalene-based self-assembled ring |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464414/ https://www.ncbi.nlm.nih.gov/pubmed/26124899 http://dx.doi.org/10.3762/bjoc.11.108 |
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