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Sequential Pore Wall Modification in a Covalent Organic Framework for Application in Lactic Acid Adsorption

Open access
Lohse, Maria S., Stassin, Timothée, Naudin, Guillaume, Wuttke, Stefan, Ameloot, Rob, De Vos, Dirk, Medina, Dana D., Bein, Thomas·2016·Chemistry of Materials

Abstract

Abstract Here we describe the synthesis and postsynthetic modification of the stable β-ketoenamine TpBD(NH2)2 covalent organic framework (COF), having primary amine groups integrated into the pore walls. For this purpose we initially synthesized the nitro version of this COF, TpBD(NO2)2. Afterward, TpBD(NO2)2 was reduced to afford the desired framework having primary amine functionality. We demonstrate the accessibility of the primary amine groups and the robustness of the framework by a second modification step, the aminolysis of acetic anhydride, to obtain the corresponding amide form TpBD(NHCOCH3)2. Taking advantage of the high stability of these frameworks under acidic conditions, we study the liquid-phase adsorption of lactic acid, revealing the strong impact of a pore wall modification on the adsorption performance.

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Metadata

Authors
Lohse, M. S., Stassin, T., Naudin, G., Wuttke, S., Ameloot, R., De Vos, D., Medina, D. D., & Bein, T.
Venue
Chemistry of Materials
Published
2016-01-04
Volume
28
Issue
2
Pages
626-631
ISSN
  • 0897-4756 (ISSN-L)
  • 1520-5002
OpenAlex
W2317592737
Cited by
233
References
1
FWCI
6.66
Type
journal article
Language
en
Open access
hybrid

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The paper
Lohse, M. S., Stassin, T., Naudin, G., Wuttke, S., Ameloot, R., De Vos, D., Medina, D. D., & Bein, T. (2016). Sequential Pore Wall Modification in a Covalent Organic Framework for Application in Lactic Acid Adsorption. Chemistry of Materials. https://doi.org/10.1021/acs.chemmater.5b04388

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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