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Oligothiophene-Bridged Conjugated Covalent Organic Frameworks
[Image: see text] Two-dimensional covalent organic frameworks (2D-COFs) are crystalline, porous materials comprising aligned columns of π-stacked building blocks. With a view toward the application of these materials in organic electronics and optoelectronics, the construction of oligothiophene-base...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400432/ https://www.ncbi.nlm.nih.gov/pubmed/28586200 http://dx.doi.org/10.1021/jacs.7b01631 |
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author | Keller, Niklas Bessinger, Derya Reuter, Stephan Calik, Mona Ascherl, Laura Hanusch, Fabian C. Auras, Florian Bein, Thomas |
author_facet | Keller, Niklas Bessinger, Derya Reuter, Stephan Calik, Mona Ascherl, Laura Hanusch, Fabian C. Auras, Florian Bein, Thomas |
author_sort | Keller, Niklas |
collection | PubMed |
description | [Image: see text] Two-dimensional covalent organic frameworks (2D-COFs) are crystalline, porous materials comprising aligned columns of π-stacked building blocks. With a view toward the application of these materials in organic electronics and optoelectronics, the construction of oligothiophene-based COFs would be highly desirable. The realization of such materials, however, has remained a challenge, in particular with respect to laterally conjugated imine-linked COFs. We have developed a new building block design employing an asymmetric modification on an otherwise symmetric backbone that allows us to construct a series of highly crystalline quaterthiophene-derived COFs with tunable electronic properties. Studying the optical response of these materials, we have observed for the first time the formation of a charge transfer state between the COF subunits across the imine bond. We believe that our new building block design provides a general strategy for the construction of well-ordered COFs from various extended building blocks, thus greatly expanding the range of applicable molecules. |
format | Online Article Text |
id | pubmed-6400432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-64004322019-03-06 Oligothiophene-Bridged Conjugated Covalent Organic Frameworks Keller, Niklas Bessinger, Derya Reuter, Stephan Calik, Mona Ascherl, Laura Hanusch, Fabian C. Auras, Florian Bein, Thomas J Am Chem Soc [Image: see text] Two-dimensional covalent organic frameworks (2D-COFs) are crystalline, porous materials comprising aligned columns of π-stacked building blocks. With a view toward the application of these materials in organic electronics and optoelectronics, the construction of oligothiophene-based COFs would be highly desirable. The realization of such materials, however, has remained a challenge, in particular with respect to laterally conjugated imine-linked COFs. We have developed a new building block design employing an asymmetric modification on an otherwise symmetric backbone that allows us to construct a series of highly crystalline quaterthiophene-derived COFs with tunable electronic properties. Studying the optical response of these materials, we have observed for the first time the formation of a charge transfer state between the COF subunits across the imine bond. We believe that our new building block design provides a general strategy for the construction of well-ordered COFs from various extended building blocks, thus greatly expanding the range of applicable molecules. American Chemical Society 2017-06-06 2017-06-21 /pmc/articles/PMC6400432/ /pubmed/28586200 http://dx.doi.org/10.1021/jacs.7b01631 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Keller, Niklas Bessinger, Derya Reuter, Stephan Calik, Mona Ascherl, Laura Hanusch, Fabian C. Auras, Florian Bein, Thomas Oligothiophene-Bridged Conjugated Covalent Organic Frameworks |
title | Oligothiophene-Bridged
Conjugated Covalent Organic
Frameworks |
title_full | Oligothiophene-Bridged
Conjugated Covalent Organic
Frameworks |
title_fullStr | Oligothiophene-Bridged
Conjugated Covalent Organic
Frameworks |
title_full_unstemmed | Oligothiophene-Bridged
Conjugated Covalent Organic
Frameworks |
title_short | Oligothiophene-Bridged
Conjugated Covalent Organic
Frameworks |
title_sort | oligothiophene-bridged
conjugated covalent organic
frameworks |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400432/ https://www.ncbi.nlm.nih.gov/pubmed/28586200 http://dx.doi.org/10.1021/jacs.7b01631 |
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