Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Karine Fournel-Marotte"'
Publikováno v:
Molecules, Vol 18, Iss 9, Pp 11553-11575 (2013)
The synthesis of a peptide-containing lasso molecular switch by a self-entanglement strategy is described. The interlocked [1] rotaxane molecular machine consists of a benzometaphenylene[25]crown-8 (BMP25C8) macrocycle surrounding a molecular axle. T
Externí odkaz:
https://doaj.org/article/bef745649fc644538d3ca2a4d8ef264b
Autor:
Victor Koehler, Maxime Gauthier, Chenhao Yao, Karine Fournel-Marotte, Philip Waelès, Brice Kauffmann, Ivan Huc, Frédéric Coutrot, Yann Ferrand
Publikováno v:
Chemical Communications
Chemical Communications, 2022, 58 (62), pp.8618-8621. ⟨10.1039/D2CC03066G⟩
Chemical Communications, 2022, 58 (62), pp.8618-8621. ⟨10.1039/D2CC03066G⟩
The wrapping of an aromatic oligoamide helix around an active ester-containing [2]rotaxane enforced the sliding and the sequestration of the surrounding macrocycle around a part of the axle for which it has no formal affinity. The foldamer-mediated c
Publikováno v:
Chemistry - A European Journal. 23
Publikováno v:
Nature chemistry. 9(2)
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2017, 23 (48), pp.11529-11539. ⟨10.1002/chem.201701912⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2017, 23 (48), pp.11529-11539. ⟨10.1002/chem.201701912⟩
International audience; This paper reports on the synthesis of a tri-stable [2]rotaxane molecular shuttle, in which the motion of the macrocycle is triggered by either selective protonation/deprotonation or specific carbamoylation/decarbamoylation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e073a11b7fd579ef094e085d42bda63b
https://hal.archives-ouvertes.fr/hal-01581078
https://hal.archives-ouvertes.fr/hal-01581078
Publikováno v:
Nature Chemistry. 9:105-106
Molecular daisy-chain structures are typically made up of two interlocked components and can exhibit muscle-like contraction and extension in one dimension. Zinc-based multicomponent systems that can operate in two and three dimensions have now been
Publikováno v:
Chemical Science
Chemical Science, The Royal Society of Chemistry, 2015, 6 (8), pp.4828-4836. ⟨10.1039/c5sc01722j⟩
Chemical Science, The Royal Society of Chemistry, 2015, 6 (8), pp.4828-4836. ⟨10.1039/c5sc01722j⟩
International audience; We report a diverted route to [1]rotaxane and tris-branched [1]rotaxane that are devoid of any efficient template and which could not be obtained by classical straightforward strategies. The described chemical route relies on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db6e812b0e010c9a94ba71a178f82959
https://hal.archives-ouvertes.fr/hal-01191700/file/c5sc01722j.pdf
https://hal.archives-ouvertes.fr/hal-01191700/file/c5sc01722j.pdf
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2014, 53 (27), pp.6914-6919. ⟨10.1002/anie.201403765⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2014, 53 (27), pp.6914-6919. ⟨10.1002/anie.201403765⟩
International audience; A general synthesis of triazolium-containing [2]rotaxanes, which could not be accessed by other methods, is reported. It is based on a sequential strategy starting from a well-designed macrocycle transporter which contains a t
Publikováno v:
Molecules
Molecules, MDPI, 2013, 18, pp.11553-11575. ⟨10.3390/molecules180911553⟩
Molecules, Vol 18, Iss 9, Pp 11553-11575 (2013)
Volume 18
Issue 9
Pages 11553-11575
Molecules, MDPI, 2013, 18, pp.11553-11575. ⟨10.3390/molecules180911553⟩
Molecules, Vol 18, Iss 9, Pp 11553-11575 (2013)
Volume 18
Issue 9
Pages 11553-11575
International audience; The synthesis of a peptide-containing lasso molecular switch by a self-entanglement strategy is described. The interlocked [1] rotaxane molecular machine consists of a benzometaphenylene[25]crown-8 (BMP25C8) macrocycle surroun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4ec1f9059674962c701f712b27df18d
https://hal.archives-ouvertes.fr/hal-00862684/file/molecules-18-11553.pdf
https://hal.archives-ouvertes.fr/hal-00862684/file/molecules-18-11553.pdf