Pierre Kuhn
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Pierre Kuhn has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
- Markus Antonietti
Max Planck Institute of Colloids and Interfaces
5 shared publications Arne Thomas
Max Planck Institute of Colloids and Interfaces Department of Colloid Chemistry Research Campus Golm, 14424 Potsdam, (Germany)
4 shared publications- Arne Thomas
Max-Planck-Institut für Kolloid- und Grenflächenforschung, Wissenschaftspark Golm, 14424 Potsdam, Deutschland, Fax: (+49) 331-567-9502
2 shared publications - Aurelien Forget
Institute for Macromolecular Chemistry Albert‐Ludwigs‐University Freiburg Stefan‐Meier‐Str. 31 79104 Freiburg Germany
2 shared publications Dangsheng Su
Max Planck Institute of Colloids and Interfaces, Department of Colloid Chemistry, Research Campus Golm, 14424 Potsdam, Germany, and Fritz Haber Institute of the Max Planck Society, Department of Inorganic Chemistry, Faradayweg 4-6, 14195 Berlin, Germany
1 shared publicationJürgen Hartmann
Max Planck Institute of Colloids and Interfaces Department of Colloid Chemistry Research Campus Golm, 14424 Potsdam, (Germany)
1 shared publication
Latest Publications
- 19 February 2009
- Published by Wiley in Advanced Materials
- Vol. 21 (8) , 897-901
Template‐Free Tuning of Nanopores in Carbonaceous Polymers through Ionothermal Synthesis
- 19 February 2009
- Published by Wiley in Advanced Materials
- Vol. 21 (8) , 897-901
Template‐Free Tuning of Nanopores in Carbonaceous Polymers through Ionothermal Synthesis
- 9 December 2008
- Published by American Chemical Society (ACS) in Macromolecules
- Vol. 42 (1) , 319-326
Toward Tailorable Porous Organic Polymer Networks: A High-Temperature Dynamic Polymerization Scheme Based on Aromatic Nitriles
- 9 December 2008
- Published by American Chemical Society (ACS) in Macromolecules
- Vol. 42 (1) , 319-326
Toward Tailorable Porous Organic Polymer Networks: A High-Temperature Dynamic Polymerization Scheme Based on Aromatic Nitriles
- 2 October 2008
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- No. 44,p. 5815-5817
“Everything is surface”: tunable polymer organic frameworks with ultrahigh dye sorption capacity
Carbonaceous polymer networks with tunable porosity were found to behave as exceptional adsorbents toward large organic molecules such as organic dyes.
- 2 October 2008
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- No. 44,p. 5815-5817
“Everything is surface”: tunable polymer organic frameworks with ultrahigh dye sorption capacity
Carbonaceous polymer networks with tunable porosity were found to behave as exceptional adsorbents toward large organic molecules such as organic dyes.
- Top Cited Papers
- 13 September 2008
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 130 (40) , 13333-13337
From Microporous Regular Frameworks to Mesoporous Materials with Ultrahigh Surface Area: Dynamic Reorganization of Porous Polymer Networks
High surface area organic materials featuring both micro- and mesopores were synthesized under ionothermal conditions via the formation of polyaryltriazine networks. While the polytrimerization of nitriles in zinc chloride at 400 °C produces microporous polymers, higher reaction temperatures induce the formation of additional spherical mesopores with a narrow dispersity. The nitrogen-rich carbonaceous polymer materials thus obtained present surface areas and porosities up to 3300 m2 g−1 and 2.4 cm3 g−1, respectively. The key point of this synthesis relies on the occurrence of several high temperature polymerization reactions, where irreversible carbonization reactions coupled with the reversible trimerization of nitriles allow the reorganization of the dynamic triazine network. The ZnCl2 molten salt fulfills the requirement of a high temperature solvent, but is also required as catalyst. Thus, this dynamic polymerization system provides not only highly micro- and mesoporous materials, but also allows controlling the pore structure in amorphous organic materials.
- 13 September 2008
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 130 (40) , 13333-13337
Top Cited PapersFrom Microporous Regular Frameworks to Mesoporous Materials with Ultrahigh Surface Area: Dynamic Reorganization of Porous Polymer Networks
High surface area organic materials featuring both micro- and mesopores were synthesized under ionothermal conditions via the formation of polyaryltriazine networks. While the polytrimerization of nitriles in zinc chloride at 400 °C produces microporous polymers, higher reaction temperatures induce the formation of additional spherical mesopores with a narrow dispersity. The nitrogen-rich carbonaceous polymer materials thus obtained present surface areas and porosities up to 3300 m2 g−1 and 2.4 cm3 g−1, respectively. The key point of this synthesis relies on the occurrence of several high temperature polymerization reactions, where irreversible carbonization reactions coupled with the reversible trimerization of nitriles allow the reorganization of the dynamic triazine network. The ZnCl2 molten salt fulfills the requirement of a high temperature solvent, but is also required as catalyst. Thus, this dynamic polymerization system provides not only highly micro- and mesoporous materials, but also allows controlling the pore structure in amorphous organic materials.
- 15 April 2008
- Published by Wiley in Angewandte Chemie
- Vol. 120 (18) , 3499-3502
Ionothermalsynthese von porösen kovalenten Triazin‐ Polymernetzwerken
- 15 April 2008
- Published by Wiley in Angewandte Chemie
- Vol. 120 (18) , 3499-3502
Ionothermalsynthese von porösen kovalenten Triazin‐ Polymernetzwerken
- Top Cited Papers
- 14 April 2008
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 47 (18) , 3450-3453
Porous, Covalent Triazine‐Based Frameworks Prepared by Ionothermal Synthesis
- 14 April 2008
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 47 (18) , 3450-3453
Top Cited PapersPorous, Covalent Triazine‐Based Frameworks Prepared by Ionothermal Synthesis