Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Victor Maurizot"'
Autor:
Albano Galan, Kristijan Lulic, Jingqi Wang, Barbara Wicher, Ivan Huc, Jean Duhamel, Victor Maurizot
Publikováno v:
Chemical Communications. 59:5253-5256
A new ligation method for piling up helical aromatic foldamers into rigid coaxial stacks has allowed the formation of discrete dimers and of dynamic supramolecular polymers.
Publikováno v:
Chemical Science. 14:3742-3751
When linked with a flexible linker, two aromatic helices displaying hydrogen bond donors and acceptors may fold back on each other. They may also generate larger complex assemblies.
Autor:
Friedericke S. Menke, Daniela Mazzier, Barbara Wicher, Lars Allmendinger, Brice Kauffmann, Victor Maurizot, Ivan Huc
Publikováno v:
Organic & Biomolecular Chemistry. 21:1275-1283
Fulfilling stabilizing hydrogen bonds in a synthetic helix–turn–helix structure may concomitantly generate conformational frustration.
Autor:
Dennis Meier, Benedikt Schoof, Jinhua Wang, Xuesong Li, Andreas Walz, Annette Huettig, Hartmut Schlichting, Frédéric Rosu, Valérie Gabelica, Victor Maurizot, Joachim Reichert, Anthoula C. Papageorgiou, Ivan Huc, Johannes V. Barth
Publikováno v:
Chemical Communications. 58:8938-8941
Aromatic foldamers are promising for applications such as molecular recognition and molecular machinery. For many of these, defect free, 2D-crystaline monolayers are needed. To this end, submonolayers were prepared in ultra-high vacuum (UHV) on Ag(11
Publikováno v:
Angewandte Chemie International Edition. 62
Publikováno v:
Chemistry – A European Journal. 28
Folded molecules provide complex interaction interfaces amenable to sophisticated self-assembly motifs. Because of their high conformational stability, aromatic foldamers constitute suitable candidates for the rational elaboration of self-assembled a
Autor:
Thierry Buffeteau, Ivan Huc, Barbara Wicher, Victor Maurizot, Alejandro Méndez-Ardoy, Gilles Pecastaings, Jinhua Wang, Xuesong Li, Dario M. Bassani
Publikováno v:
Angewandte Chemie. 133:18609-18614
The very stable helices of 8-amino-2-quinolinecar-boxylic acid oligoamides are shown to uptake CuIIions in theircavity through deprotonation of their amide functions with minimal alteration of their shape, unlike most metallo-organicstructures which
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2020, ⟨10.1002/chem.202003559⟩
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2020, ⟨10.1002/chem.202003559⟩
Quinoline based aromatic amide foldamers are known to adopt stable folded conformations. We have developed a synthetic approach to produce similar oligomers where all amide bonds, or part of them, have been replaced by an isosteric vinylene group. Th
Autor:
Bappaditya Gole, Brice Kauffmann, Arnaud Tron, Victor Maurizot, Nathan McClenaghan, Ivan Huc, Yann Ferrand
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, 2022, 144 (15), pp.6894-6906. ⟨10.1021/jacs.2c01269⟩
Journal of the American Chemical Society, 2022, 144 (15), pp.6894-6906. ⟨10.1021/jacs.2c01269⟩
International audience; A series of aromatic helix-sheet-helix oligoamide foldamers composed of several different photosensitive diazaanthracene units have been designed and synthesized. Molecular objects up to 7 kDa were straightforwardly produced o
Umfangreiche Konformationsänderungen in selbstassemblierten mehrsträngigen aromatischen Faltblättern
Publikováno v:
Angewandte Chemie. 133:2605-2609