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Squarephaneic Tetraanhydride: A Conjugated Square‐Shaped Cyclophane for the Synthesis of Porous Organic Materials
Aromatic carboxylic anhydrides are ubiquitous building blocks in organic materials chemistry and have received considerable attention in the synthesis of organic semiconductors, pigments, and battery electrode materials. Here we extend the family of aromatic carboxylic anhydrides with a unique new m...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827958/ https://www.ncbi.nlm.nih.gov/pubmed/36178733 http://dx.doi.org/10.1002/anie.202212623 |
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author | Eder, Simon Ding, Bowen Thornton, Daisy B. Sammut, Darlene White, Andrew J. P. Plasser, Felix Stephens, Ifan E. L. Heeney, Martin Mezzavilla, Stefano Glöcklhofer, Florian |
author_facet | Eder, Simon Ding, Bowen Thornton, Daisy B. Sammut, Darlene White, Andrew J. P. Plasser, Felix Stephens, Ifan E. L. Heeney, Martin Mezzavilla, Stefano Glöcklhofer, Florian |
author_sort | Eder, Simon |
collection | PubMed |
description | Aromatic carboxylic anhydrides are ubiquitous building blocks in organic materials chemistry and have received considerable attention in the synthesis of organic semiconductors, pigments, and battery electrode materials. Here we extend the family of aromatic carboxylic anhydrides with a unique new member, a conjugated cyclophane with four anhydride groups. The cyclophane is obtained in a three‐step synthesis and can be functionalised efficiently, as shown by the conversion into tetraimides and an octacarboxylate. Crystal structures reveal the high degree of porosity achievable with the new building block. Excellent electrochemical properties and reversible reduction to the tetraanions are shown for the imides; NMR and EPR measurements confirm the global aromaticity of the dianions and evidence the global Baird aromaticity of the tetraanions. Considering the short synthesis and unique properties, we expect widespread use of the new building block in the development of organic materials. |
format | Online Article Text |
id | pubmed-9827958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98279582023-01-10 Squarephaneic Tetraanhydride: A Conjugated Square‐Shaped Cyclophane for the Synthesis of Porous Organic Materials Eder, Simon Ding, Bowen Thornton, Daisy B. Sammut, Darlene White, Andrew J. P. Plasser, Felix Stephens, Ifan E. L. Heeney, Martin Mezzavilla, Stefano Glöcklhofer, Florian Angew Chem Int Ed Engl Research Articles Aromatic carboxylic anhydrides are ubiquitous building blocks in organic materials chemistry and have received considerable attention in the synthesis of organic semiconductors, pigments, and battery electrode materials. Here we extend the family of aromatic carboxylic anhydrides with a unique new member, a conjugated cyclophane with four anhydride groups. The cyclophane is obtained in a three‐step synthesis and can be functionalised efficiently, as shown by the conversion into tetraimides and an octacarboxylate. Crystal structures reveal the high degree of porosity achievable with the new building block. Excellent electrochemical properties and reversible reduction to the tetraanions are shown for the imides; NMR and EPR measurements confirm the global aromaticity of the dianions and evidence the global Baird aromaticity of the tetraanions. Considering the short synthesis and unique properties, we expect widespread use of the new building block in the development of organic materials. John Wiley and Sons Inc. 2022-10-25 2022-11-25 /pmc/articles/PMC9827958/ /pubmed/36178733 http://dx.doi.org/10.1002/anie.202212623 Text en © 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Eder, Simon Ding, Bowen Thornton, Daisy B. Sammut, Darlene White, Andrew J. P. Plasser, Felix Stephens, Ifan E. L. Heeney, Martin Mezzavilla, Stefano Glöcklhofer, Florian Squarephaneic Tetraanhydride: A Conjugated Square‐Shaped Cyclophane for the Synthesis of Porous Organic Materials |
title | Squarephaneic Tetraanhydride: A Conjugated Square‐Shaped Cyclophane for the Synthesis of Porous Organic Materials
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title_full | Squarephaneic Tetraanhydride: A Conjugated Square‐Shaped Cyclophane for the Synthesis of Porous Organic Materials
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title_fullStr | Squarephaneic Tetraanhydride: A Conjugated Square‐Shaped Cyclophane for the Synthesis of Porous Organic Materials
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title_full_unstemmed | Squarephaneic Tetraanhydride: A Conjugated Square‐Shaped Cyclophane for the Synthesis of Porous Organic Materials
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title_short | Squarephaneic Tetraanhydride: A Conjugated Square‐Shaped Cyclophane for the Synthesis of Porous Organic Materials
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title_sort | squarephaneic tetraanhydride: a conjugated square‐shaped cyclophane for the synthesis of porous organic materials |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827958/ https://www.ncbi.nlm.nih.gov/pubmed/36178733 http://dx.doi.org/10.1002/anie.202212623 |
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