direkt zum Inhalt springen

direkt zum Hauptnavigationsmenü

Sie sind hier

TU Berlin

Page Content

Convalent Organic Frameworks

Lupe

Covalent organic frameworks are covalently connected, purely organic structures with extended, periodic architectures in two or three dimensions. In general, for the formation of COFs it is necessary that the condensation reaction occur in a reversible or dynamic fashion, that is, chemical bonds of the forming polymer network have to close and open, yielding in consequence the thermodynamically (meta)stable, yet crystalline structure. To create covalently bound organic frameworks, either covalent bonding schemes have to be identified which are rather weak and thus can reopen under mild conditions, or harsher reaction conditions have to be applied which however have to selectively and reversibly open and close on certain bond in the network. COFs have been synthesized in our group by trimerization of dicyano-compounds. To enable reversibility, the reaction had to be carried out under much harsher reaction conditions. Trimerization of 1,4-dicyanobenzene in molten zinc chloride at 400°C yield covalent triazine-based frameworks (CTF) with high chemical and thermal robustness. The synthesis in salt melts also allow to prepare networks at even higher temperatures yielding materials with hierarchical pore structures and high surface areas of up to 3000 m2/g. The formation of the triazine rings inherently yield a high amount of heteroatoms in the networks which can be used for example for the coordination and thus stabilization of metal nanoparticles creating active and stable catalysts.

Relevant Publications

Covalent Triazine Framework as Catalytic Support for Liquid Phase Reaction C. E. Chan-Thaw, A. Villa, P. Katekomol, D. S. Su, A. Thomas, L. Prati, Nano Lett.2010, 10, 537
Solid Catalysts for the Selective Low-Temperature Oxidation of Methane to Methanol R. Palkovits, M. Antonietti, P. Kuhn, A. Thomas, F. Schuth, Angew. Chem.Int. Ed. 2009, 48, 6909
“Toward Tailorable Porous Organic Polymer Networks: A High-Temperature Dynamic Polymerization Scheme Based on Aromatic Nitriles P. Kuhn, A. Thomas, M. Antonietti, Macromolecules 2009, 42, 319-326
Template-Free Tuning of Nanopores in Carbonaceous Polymers through Ionothermal Synthesis
P. Kuhn, A. Forget, J. Hartmann, A. Thomas, M. Antonietti, Adv. Mater. 2009, 21, 897-901
Everything is surface: tunable polymer organic frameworks with ultrahigh dye sorption capacity
P. Kuhn, K. Krüger, A. Thomas, M. Antonietti, Chem. Commun. 2008, 5815-5817
From Microporous Regular Frameworks to Mesoporous Materials with Ultrahigh Surface Area: Dynamic Reorganization of Porous Polymer Networks P. Kuhn, A. Forget, D. Su, A. Thomas, M. Antonietti, J. Amer. Chem. 2008, 130, 13333-13337
Porous, Covalent Triazine-Based Organic Frameworks Prepared by Ionothermal Synthesis P. Kuhn, M. Antonietti, A. Thomas, Angew. Chem. Int. Ed. 2008, 47, 3450-3453

Zusatzinformationen / Extras

Quick Access:

Schnellnavigation zur Seite über Nummerneingabe

Auxiliary Functions

This site uses Matomo for anonymized webanalysis. Visit Data Privacy for more information and opt-out options.

Prof. Dr. Arne Thomas
Functional Materials

Secretary
Anne Svilarov
Functional Materials
sec. BA2
Tel.: +49 30 314 25118
Fax: +49 30 314 29271

Address
TU Berlin
Fak. II
Institute of Chemistry
Functional Materials
Room 216
Hardenbergstraße 40
10623 Berlin