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From Highly Crystalline to Outer Surface-Functionalized Covalent Organic Frameworks—A Modulation Approach

[Image: see text] Crystallinity and porosity are of central importance for many properties of covalent organic frameworks (COFs), including adsorption, diffusion, and electronic transport. We have developed a new method for strongly enhancing both aspects through the introduction of a modulating age...

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Autores principales: Calik, Mona, Sick, Torben, Dogru, Mirjam, Döblinger, Markus, Datz, Stefan, Budde, Harald, Hartschuh, Achim, Auras, Florian, Bein, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742964/
https://www.ncbi.nlm.nih.gov/pubmed/26694214
http://dx.doi.org/10.1021/jacs.5b10708
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author Calik, Mona
Sick, Torben
Dogru, Mirjam
Döblinger, Markus
Datz, Stefan
Budde, Harald
Hartschuh, Achim
Auras, Florian
Bein, Thomas
author_facet Calik, Mona
Sick, Torben
Dogru, Mirjam
Döblinger, Markus
Datz, Stefan
Budde, Harald
Hartschuh, Achim
Auras, Florian
Bein, Thomas
author_sort Calik, Mona
collection PubMed
description [Image: see text] Crystallinity and porosity are of central importance for many properties of covalent organic frameworks (COFs), including adsorption, diffusion, and electronic transport. We have developed a new method for strongly enhancing both aspects through the introduction of a modulating agent in the synthesis. This modulator competes with one of the building blocks during the solvothermal COF growth, resulting in highly crystalline frameworks with greatly increased domain sizes reaching several hundreds of nanometers. The obtained materials feature fully accessible pores with an internal surface area of over 2000 m(2) g(–1). Compositional analysis via NMR spectroscopy revealed that the COF-5 structure can form over a wide range of boronic acid-to-catechol ratios, thus producing frameworks with compositions ranging from highly boronic acid-deficient to networks with catechol voids. Visualization of an −SH-functionalized modulating agent via iridium staining revealed that the COF domains are terminated by the modulator. Using functionalized modulators, this synthetic approach thus also provides a new and facile method for the external surface functionalization of COF domains, providing accessible sites for post-synthetic modification reactions. We demonstrate the feasibility of this concept by covalently attaching fluorescent dyes and hydrophilic polymers to the COF surface. We anticipate that the realization of highly crystalline COFs with the option of additional surface functionality will render the modulation concept beneficial for a range of applications, including gas separations, catalysis, and optoelectronics.
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spelling pubmed-47429642016-02-16 From Highly Crystalline to Outer Surface-Functionalized Covalent Organic Frameworks—A Modulation Approach Calik, Mona Sick, Torben Dogru, Mirjam Döblinger, Markus Datz, Stefan Budde, Harald Hartschuh, Achim Auras, Florian Bein, Thomas J Am Chem Soc [Image: see text] Crystallinity and porosity are of central importance for many properties of covalent organic frameworks (COFs), including adsorption, diffusion, and electronic transport. We have developed a new method for strongly enhancing both aspects through the introduction of a modulating agent in the synthesis. This modulator competes with one of the building blocks during the solvothermal COF growth, resulting in highly crystalline frameworks with greatly increased domain sizes reaching several hundreds of nanometers. The obtained materials feature fully accessible pores with an internal surface area of over 2000 m(2) g(–1). Compositional analysis via NMR spectroscopy revealed that the COF-5 structure can form over a wide range of boronic acid-to-catechol ratios, thus producing frameworks with compositions ranging from highly boronic acid-deficient to networks with catechol voids. Visualization of an −SH-functionalized modulating agent via iridium staining revealed that the COF domains are terminated by the modulator. Using functionalized modulators, this synthetic approach thus also provides a new and facile method for the external surface functionalization of COF domains, providing accessible sites for post-synthetic modification reactions. We demonstrate the feasibility of this concept by covalently attaching fluorescent dyes and hydrophilic polymers to the COF surface. We anticipate that the realization of highly crystalline COFs with the option of additional surface functionality will render the modulation concept beneficial for a range of applications, including gas separations, catalysis, and optoelectronics. American Chemical Society 2015-12-22 2016-02-03 /pmc/articles/PMC4742964/ /pubmed/26694214 http://dx.doi.org/10.1021/jacs.5b10708 Text en Copyright © 2015 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Calik, Mona
Sick, Torben
Dogru, Mirjam
Döblinger, Markus
Datz, Stefan
Budde, Harald
Hartschuh, Achim
Auras, Florian
Bein, Thomas
From Highly Crystalline to Outer Surface-Functionalized Covalent Organic Frameworks—A Modulation Approach
title From Highly Crystalline to Outer Surface-Functionalized Covalent Organic Frameworks—A Modulation Approach
title_full From Highly Crystalline to Outer Surface-Functionalized Covalent Organic Frameworks—A Modulation Approach
title_fullStr From Highly Crystalline to Outer Surface-Functionalized Covalent Organic Frameworks—A Modulation Approach
title_full_unstemmed From Highly Crystalline to Outer Surface-Functionalized Covalent Organic Frameworks—A Modulation Approach
title_short From Highly Crystalline to Outer Surface-Functionalized Covalent Organic Frameworks—A Modulation Approach
title_sort from highly crystalline to outer surface-functionalized covalent organic frameworks—a modulation approach
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742964/
https://www.ncbi.nlm.nih.gov/pubmed/26694214
http://dx.doi.org/10.1021/jacs.5b10708
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