Zobrazeno 1 - 10
of 148
pro vyhledávání: '"Jan O. Jeppesen"'
Autor:
Mathias S. Neumann, Amanda F. Smith, Sofie K. Jensen, Rikke Frederiksen, Mathias L. Skavenborg, Jan O. Jeppesen
Publikováno v:
Chemical Communications. 59:6335-6338
An out-of-equilibrium bistable [2]rotaxane was used to make a complete profiling of the energy landscape when a tetracationic ring (blue) moves across a stimuli-induced electrostatic barrier (green) carrying two positive charges.
Autor:
Rikke Kristensen, Mathias S. Neumann, Sissel S. Andersen, Paul C. Stein, Amar H. Flood, Jan O. Jeppesen
Publikováno v:
Kristensen, R, Neumann, M S, Andersen, S S, Stein, P C, Flood, A H & Jeppesen, J O 2022, ' Quantifying the barrier for the movement of cyclobis(paraquat-p-phenylene) over the dication of monopyrrolotetrathiafulvalene ', Organic & Biomolecular Chemistry, vol. 20, no. 11, pp. 2233-2248 . https://doi.org/10.1039/d1ob02263f
A bistable [2]pseudorotaxane 1⊂CBPQT·4PF6 and a bistable [2]rotaxane 2·4PF6 have been synthesised to measure the height of an electrostatic barrier produced by double molecular oxidation (0 to +2). Both systems have monopyrrolotetrathiafulvalene
Autor:
Luke J. O’Driscoll, Sissel S. Andersen, Marta V. Solano, Dan Bendixen, Morten Jensen, Troels Duedal, Jess Lycoops, Cornelia van der Pol, Rebecca E. Sørensen, Karina R. Larsen, Kenneth Myntman, Christian Henriksen, Stinne W. Hansen, Jan O. Jeppesen
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 1112-1122 (2015)
The electron-donor and unique redox properties of the tetrathiafulvalene (TTF, 1) moiety have led to diverse applications in many areas of chemistry. Monopyrrolotetrathiafulvalenes (MPTTFs, 4) and bispyrrolotetrathiafulvalenes (BPTTFs, 5) are useful
Externí odkaz:
https://doaj.org/article/92c2979bbee14b42bd2077ef60ae3b96
Publikováno v:
Jensen, M, Kristensen, R, Andersen, S S, Bendixen, D & Jeppesen, J O 2020, ' Probing the Electrostatic Barrier of Tetrathiafulvalene Dications using a Tetra-stable Donor–Acceptor [2]Rotaxane ', Chemistry-A European Journal, vol. 26, no. 28, pp. 6165-6175 . https://doi.org/10.1002/chem.202000302
A tetra-stable donor–acceptor [2]rotaxane 1⋅4PF6 has been synthesized. The dumbbell component is comprised of an oxyphenylene (OP), a tetrathiafulvalene (TTF), a monopyrrolo-TTF (MPTTF), and a hydroquinone (HQ) unit, which can act as recognition
Publikováno v:
European Journal of Organic Chemistry. 2019:7532-7540
Publikováno v:
Bähring, S, Root, H D, Sessler, J L & Jeppesen, J O 2019, ' Tetrathiafulvalene-calix[4]pyrrole : a versatile synthetic receptor for electron-deficient planar and spherical guests ', Organic & Biomolecular Chemistry, vol. 17, no. 10, pp. 2594-2613 . https://doi.org/10.1039/c8ob02514b
The first tetrakis-tetrathiafulvalene-calix[4]pyrrole (TTF-C[4]P) was reported in 2004. Early on it and related π-extended TTF-C[4]Ps were found to function as both anion receptors and as hosts for planar electron deficient neutral guests, including
Publikováno v:
Jensen, M, Kristensen, R, Andersen, S S, Bendixen, D & Jeppesen, J O 2020, ' Cover Feature: Probing the Electrostatic Barrier of Tetrathiafulvalene Dications using a Tetra-stable Donor–Acceptor [2]Rotaxane (Chem. Eur. J. 28/2020) ', Chemistry-A European Journal, vol. 26, no. 28, pp. 6087-6087 . https://doi.org/10.1002/chem.202000973
Control of directionality is of paramount importance if rectified motion in electroactive molecular machines should be realized. As illustrated in the cover artwork, the tetracationic ring (blue) in a tetraoxidized [2]rotaxane can follow two differen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f5ae072906f19231a9a02d5f2b57cc0
https://portal.findresearcher.sdu.dk/da/publications/46ba955d-3bd1-410e-8bf0-4f25cea7d52b
https://portal.findresearcher.sdu.dk/da/publications/46ba955d-3bd1-410e-8bf0-4f25cea7d52b
Autor:
Kazuo Takimiya, Charlotte Burgdorf Guldager Rasmussen, Jan O. Jeppesen, Eric Levillain, Eigo Miyazaki, Jacob Kongsted, Gunnar Olsen, Troels Duedal, Tony Breton, Steffen Bähring, Kent A. Nielsen
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2017, 82 (4), pp.2123-2128. ⟨10.1021/acs.joc.6b02944⟩
Duedal, T, Nielsen, K, Olsen, G, Burgdorf Guldager Rasmussen, C, Kongsted, J, Levillain, E, Breton, T, Miyazaki, E, Takimiya, K, Bähring, S & Jeppesen, J O 2017, ' Very Strong Binding for a Neutral Calix[4]pyrrole Receptor Displaying Positive Allosteric Binding ', Journal of Organic Chemistry, vol. 82, no. 4, pp. 2123–2128 . https://doi.org/10.1021/acs.joc.6b02944
Journal of Organic Chemistry, American Chemical Society, 2017, 82 (4), pp.2123-2128. ⟨10.1021/acs.joc.6b02944⟩
Duedal, T, Nielsen, K, Olsen, G, Burgdorf Guldager Rasmussen, C, Kongsted, J, Levillain, E, Breton, T, Miyazaki, E, Takimiya, K, Bähring, S & Jeppesen, J O 2017, ' Very Strong Binding for a Neutral Calix[4]pyrrole Receptor Displaying Positive Allosteric Binding ', Journal of Organic Chemistry, vol. 82, no. 4, pp. 2123–2128 . https://doi.org/10.1021/acs.joc.6b02944
The dual-analyte responsive behavior of tetraTTF-calix[4]pyrrole receptor 1 has been shown to complex electron-deficient planar guests in a 2:1 fashion by adopting a so-called 1,3-alternate conformation. However, stronger 1:1 complexes have been demo
Publikováno v:
Kristensen, R, Andersen, S S, Olsen, G & Jeppesen, J O 2017, ' Probing the Role of Glycol Chain Lengths in π-Donor–Acceptor [2]Pseudorotaxanes Based on Monopyrrolo-Tetrathiafulvalene and Cyclobis(paraquat-p-phenylene) ', The Journal of Organic Chemistry, bind 82, nr. 3, s. 1371-1379 . https://doi.org/10.1021/acs.joc.6b02466
We have investigated and quantified the role that the glycol chain length has on the strength of the noncovalent bonding interactions taking place between cyclobis(paraquat-p-phenylene) (CBPQT4+) and five different monopyrrolo-tetrathiafulvalene (MPT
Autor:
María D. Marcos, Lluís Pascual, Jan O. Jeppesen, Ramón Martínez-Máñez, Beatriz Lozano-Torres, Andrea Bernardos, Félix Sancenón, Yolanda Salinas
Publikováno v:
Lozano-Torres, B, Pascual, L, Bernardos, A, Marcos, M D, Jeppesen, J O, Salinas, Y, Martínez-Mánez, R & Sancenón, F 2017, ' Pseudorotaxane capped mesoporous silica nanoparticles for 3,4-methylenedioxymethamphetamine (MDMA) detection in water ', Chemical Communications, vol. 53, no. 25, pp. 3559-3562 . https://doi.org/10.1039/c7cc00186j
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
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RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
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[EN] Mesoporous silica nanoparticles loaded with fluorescein and capped by a pseudorotaxane, formed between a naphthalene derivative and cyclobis(paraquat-p-phenylene) (CBPQT(4+)), were used for the selective and sensitive fluorogenic detection of 3,