| Year |
Citation |
Score |
| 2021 |
Herasymchuk K, Allain M, MacNeil GA, Carré V, Aubriet F, Leznoff DB, Sallé M, Goeb S, Storr T. Exciton Coupling in Redox-Active Salen based Self-Assembled Metallacycles. Chemistry (Weinheim An Der Bergstrasse, Germany). 27: 16161-16172. PMID 34595790 DOI: 10.1002/chem.202102745 |
0.307 |
|
| 2021 |
Goeb S, Sallé M, Siri O, Pascal S, Dekhtiarenko M, Elhabiri M, Mazan V, Canevet D, Allain M, Carré V, Aubriet F, Voitenko Z. Reversible pH-Controlled Catenation of a Benzobisimidazole-based Tetranuclear Rectangle. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34478209 DOI: 10.1002/chem.202103039 |
0.693 |
|
| 2021 |
Goeb S, Sallé M. Electron-rich Coordination Receptors Based on Tetrathiafulvalene Derivatives: Controlling the Host-Guest Binding. Accounts of Chemical Research. 54: 1043-1055. PMID 33528243 DOI: 10.1021/acs.accounts.0c00828 |
0.332 |
|
| 2021 |
Choisnet T, Canevet D, Sallé M, Lorthioir C, Bouteiller L, Woisel P, Niepceron F, Nicol E, Colombani O. Colored Janus Nanocylinders Driven by Supramolecular Coassembly of Donor and Acceptor Building Blocks. Acs Nano. 15: 2569-2577. PMID 33512151 DOI: 10.1021/acsnano.0c07039 |
0.706 |
|
| 2020 |
Gainar A, Lai TL, Oliveras-Gonzalez C, Pop F, Raynal M, Isare B, Bouteiller L, Linares M, Canevet D, Avarvari N, Sallé M. Tuning the organogelating and spectroscopic properties of a C3-symmetric pyrene-based gelator through charge transfer. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33175405 DOI: 10.1002/chem.202003914 |
0.697 |
|
| 2020 |
Dekhtiarenko M, Krykun S, Carré V, Aubriet F, Canevet D, Allain M, Voitenko Z, Sallé M, Goeb S. Tuning the structure and the properties of dithiafulvene metalla-assembled tweezers Organic Chemistry Frontiers. 7: 2040-2046. DOI: 10.1039/D0Qo00641F |
0.737 |
|
| 2019 |
Ðorđević L, Valentini C, Demitri N, Folli A, Murphy D, Meziere C, Allain M, Sallé M, Mañas-Valero S, Coronado E, Bonifazi D. O-doped nanographenes: the pyrano/pyrylium route towards semiconducting cationic mixed valence complexes. Angewandte Chemie (International Ed. in English). PMID 31889372 DOI: 10.1002/Anie.201914025 |
0.369 |
|
| 2019 |
Krykun S, Dekhtiarenko M, Canevet D, Carré V, Aubriet F, Levillain E, Allain M, Voitenko Z, Sallé M, Goeb S. Metalla-Assembled Electron-Rich Tweezers: Original Redox-Controlled Guest Release through Supramolecular Dimerization. Angewandte Chemie (International Ed. in English). PMID 31670452 DOI: 10.1002/Anie.201912016 |
0.725 |
|
| 2019 |
Choisnet T, Canevet D, Sallé M, Nicol E, Niepceron F, Jestin J, Colombani O. Robust supramolecular nanocylinders of naphthalene diimide in water. Chemical Communications (Cambridge, England). PMID 31329201 DOI: 10.1039/C9Cc04723A |
0.696 |
|
| 2019 |
Adam C, Faour L, Bonnin V, Breton T, Levillain E, Sallé M, Gautier C, Canevet D. Supramolecular chemistry of helical foldamers at the solid-liquid interface: self-assembled monolayers and anion recognition. Chemical Communications (Cambridge, England). 55: 8426-8429. PMID 31259345 DOI: 10.1039/C9Cc03851E |
0.717 |
|
| 2019 |
Herasymchuk K, Miller JJ, MacNeil GA, Sergeenko AS, McKearney D, Goeb S, Sallé M, Leznoff DB, Storr T. Coordination-driven assembly of a supramolecular square and oxidation to a tetra-ligand radical species. Chemical Communications (Cambridge, England). PMID 31066383 DOI: 10.1039/C9Cc02320H |
0.353 |
|
| 2019 |
Faour L, Adam C, Gautier C, Goeb S, Allain M, Levillain E, Canevet D, Sallé M. Redox-controlled hybridization of helical foldamers. Chemical Communications (Cambridge, England). PMID 31038524 DOI: 10.1039/C9Cc02498K |
0.692 |
|
| 2018 |
Jana A, Bähring S, Ishida M, Goeb S, Canevet D, Sallé M, Jeppesen JO, Sessler JL. Functionalised tetrathiafulvalene- (TTF-) macrocycles: recent trends in applied supramolecular chemistry. Chemical Society Reviews. 47: 5614-5645. PMID 30033473 DOI: 10.1039/C8Cs00035B |
0.705 |
|
| 2018 |
Szalóki G, Krykun S, Croué V, Allain M, Morille Y, Aubriet F, Carré V, Voitenko Z, Goeb S, Sallé M. Redox-Driven Transformation of a Discrete Molecular Cage into an Infinite 3D Coordination Polymer. Chemistry (Weinheim An Der Bergstrasse, Germany). 24: 11273-11277. PMID 29920805 DOI: 10.1002/Chem.201801653 |
0.401 |
|
| 2018 |
Belén Marco A, Gindre D, Iliopoulos K, Franco S, Andreu R, Canevet D, Sallé M. (Super)gelators derived from push-pull chromophores: synthesis, gelling properties and second harmonic generation. Organic & Biomolecular Chemistry. PMID 29561017 DOI: 10.1039/C8Ob00251G |
0.739 |
|
| 2018 |
Colomban C, Fuertes-Espinosa C, Goeb S, Sallé M, Costas M, Blancafort L, Ribas X. Self-assembled Cofacial Zinc Porphyrin Supramolecular Nanocapsules as tuneable 1O2 Photosensitizers. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29315876 DOI: 10.1002/Chem.201705531 |
0.365 |
|
| 2018 |
Krykun S, Croué V, Allain M, Voitenko Z, Aragó J, Ortí E, Goeb S, Sallé M. Tuning the electronic properties and the planarity degree in the π-extended TTF series: the prominent role of heteroatoms Journal of Materials Chemistry C. 6: 13190-13196. DOI: 10.1039/C8Tc04730H |
0.412 |
|
| 2017 |
Szalóki G, Croué V, Carré V, Aubriet F, Alévêque O, Levillain E, Allain M, Aragó J, Ortí E, Goeb S, Sallé M. Controlling the Host-Guest Interaction Mode through a Redox Stimulus. Angewandte Chemie (International Ed. in English). 56: 16272-16276. PMID 29083516 DOI: 10.1002/Anie.201709483 |
0.332 |
|
| 2017 |
Aparicio F, Faour L, Allain M, Canevet D, Sallé M. A pyrene-functionalized foldamer: structural impact and recognition properties supported by donor-acceptor interactions. Chemical Communications (Cambridge, England). PMID 29058742 DOI: 10.1039/C7Cc07253H |
0.732 |
|
| 2017 |
Colomban C, Szalóki G, Allain M, Gómez L, Goeb S, Sallé M, Costas M, Ribas X. Reversible C60 ejection from a metallocage through the redox-dependent binding of a competitive guest. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28112436 DOI: 10.1002/Chem.201700273 |
0.334 |
|
| 2017 |
Croué V, Krykun S, Allain M, Morille Y, Aubriet F, Carré V, Voitenko Z, Goeb S, Sallé M. A self-assembled M2L4 cage incorporating electron-rich 9-(1,3-dithiol-2-ylidene)fluorene units New Journal of Chemistry. 41: 3238-3241. DOI: 10.1039/C7Nj00062F |
0.411 |
|
| 2016 |
Bastien G, Dron PI, Vincent M, Canevet D, Allain M, Goeb S, Sallé M. C Recognition from Extended Tetrathiafulvalene Bis-acetylide Platinum(II) Complexes. Organic Letters. 18: 5856-5859. PMID 27788006 DOI: 10.1021/Acs.Orglett.6B02915 |
0.714 |
|
| 2016 |
Aparicio F, Faour L, Gindre D, Canevet D, Sallé M. Supramolecular control over the structural organization of a second-order NLO-active organogelator. Soft Matter. PMID 27722741 DOI: 10.1039/C6Sm01836J |
0.734 |
|
| 2016 |
Szalóki G, Croué V, Allain M, Goeb S, Sallé M. Neutral versus polycationic coordination cages: a comparison regarding neutral guest inclusion. Chemical Communications (Cambridge, England). PMID 27440274 DOI: 10.1039/C6Cc04610J |
0.393 |
|
| 2016 |
Marco AB, Aparicio F, Faour L, Iliopoulos K, Morille Y, Allain M, Franco S, Andreu R, Sahraoui B, Gindre D, Canevet D, Sallé M. Promoting Spontaneous Second Harmonic Generation through Organogelation. Journal of the American Chemical Society. 138: 9025-8. PMID 27415660 DOI: 10.1021/Jacs.6B04554 |
0.706 |
|
| 2016 |
Lai TL, Pop F, Melan C, Canevet D, Sallé M, Avarvari N. Triggering gel formation and luminescence through donor-acceptor interactions in a C3-symmetric tris(pyrene) system. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26864120 DOI: 10.1002/Chem.201600072 |
0.719 |
|
| 2016 |
Croué V, Goeb S, Szalóki G, Allain M, Sallé M. Reversible Guest Uptake/Release by Redox-Controlled Assembly/Disassembly of a Coordination Cage. Angewandte Chemie (International Ed. in English). 55: 1746-50. PMID 26693832 DOI: 10.1002/Anie.201509265 |
0.397 |
|
| 2016 |
Lai T, Pop F, Melan C, Canevet D, Sallé M, Avarvari N. Back Cover: Triggering Gel Formation and Luminescence through Donor-Acceptor Interactions in a C
3
-Symmetric Tris(pyrene) System (Chem. Eur. J. 17/2016) Chemistry - a European Journal. 22: 6124-6124. DOI: 10.1002/Chem.201601011 |
0.698 |
|
| 2015 |
Bivaud S, Goeb S, Croué V, Allain M, Pop F, Sallé M. Tuning the size of a redox-active tetrathiafulvalene-based self-assembled ring. Beilstein Journal of Organic Chemistry. 11: 966-71. PMID 26124899 DOI: 10.3762/Bjoc.11.108 |
0.348 |
|
| 2015 |
Lai TL, Canevet D, Avarvari N, Sallé M. Internal Probing of the Supramolecular Organization of Pyrene-Based Organogelators. Chemistry, An Asian Journal. PMID 26077967 DOI: 10.1002/Asia.201500395 |
0.711 |
|
| 2015 |
Croué V, Goeb S, Sallé M. Metal-driven self-assembly: the case of redox-active discrete architectures Chemical Communications. 51: 7275-7289. PMID 25812077 DOI: 10.1039/C5Cc00597C |
0.39 |
|
| 2015 |
Zitouni A, Hamel A, Bouguessa S, Gouasmia A, El-Ghayoury A, Frère P, Sallé M. Synthesis, spectroscopic and electrochemical properties of new covalent assemblies between TTF and various acceptors Synthetic Metals. 204: 84-89. DOI: 10.1016/J.Synthmet.2015.02.039 |
0.44 |
|
| 2014 |
Goeb S, Bivaud S, Croué V, Vajpayee V, Allain M, Sallé M. A Self-Assembled Electro-Active M8L4 Cage Based on Tetrathiafulvalene Ligands. Materials (Basel, Switzerland). 7: 611-622. PMID 28788478 DOI: 10.3390/Ma7010611 |
0.348 |
|
| 2014 |
Lai T, Canevet D, Almohamed Y, Mévellec J, Barillé R, Avarvari N, Sallé M. Revisiting urea-based gelators: strong solvent- and casting-microstructure dependencies and organogel processing using an alumina template New J. Chem.. 38: 4448-4457. DOI: 10.1039/C4Nj00681J |
0.683 |
|
| 2014 |
Vajpayee V, Bivaud S, Goeb S, Croué V, Allain M, Popp BV, Garci A, Therrien B, Sallé M. Electron-rich arene-ruthenium metalla-architectures incorporating tetrapyridyl-tetrathiafulvene donor moieties Organometallics. 33: 1651-1658. DOI: 10.1021/Om401142J |
0.423 |
|
| 2014 |
Belhadj E, El-Ghayoury A, Cauchy T, Allain M, Mazari M, Sallé M. Tetrathiafulvalene-based phenanthroline ligands: Synthesis, crystal structures, and electronic properties European Journal of Inorganic Chemistry. DOI: 10.1002/Ejic.201402073 |
0.397 |
|
| 2014 |
Bivaud S, Goeb S, Balandier JY, Chas M, Allain M, Sallé M. Self-assembled cages from the electroactive bis(pyrrolo)tetrathiafulvalene (BPTTF) building block European Journal of Inorganic Chemistry. 2440-2448. DOI: 10.1002/Ejic.201400060 |
0.423 |
|
| 2014 |
Canevet D, Repussard V, Sallé M. Multifunctional Photo‐ and Redox‐Active Tetrathiafulvalene‐based Organogelators: A Modular Approach Asian Journal of Organic Chemistry. 3: 216-224. DOI: 10.1002/Ajoc.201300261 |
0.687 |
|
| 2013 |
Bivaud S, Goeb S, Croué V, Dron PI, Allain M, Sallé M. Self-assembled containers based on extended tetrathiafulvalene. Journal of the American Chemical Society. 135: 10018-21. PMID 23795694 DOI: 10.1021/Ja404072W |
0.37 |
|
| 2013 |
Belhadj E, El-Ghayoury A, Ripaud E, Zorina L, Allain M, Batail P, Mazari M, Sallé M. Terpyridine-tetrathiafulvalene hybrid ligands and their electroactive metal complexes New Journal of Chemistry. 37: 1427-1436. DOI: 10.1039/C3Nj00041A |
0.362 |
|
| 2013 |
Belhadj E, El-Ghayoury A, Mazari M, Sallé M. The parent tetrathiafulvalene-terpyridine dyad: Synthesis and metal binding properties Tetrahedron Letters. 54: 3051-3054. DOI: 10.1016/J.Tetlet.2013.03.102 |
0.371 |
|
| 2013 |
Zhao B, Liu L, Li X, Qu G, Belhadj E, Derf FL, Sallé M. Ferrocenyl-triazolyl-tetrathiafulvalene assemblies: synthesis and electrochemical recognition properties Tetrahedron Letters. 54: 23-26. DOI: 10.1016/J.Tetlet.2012.10.107 |
0.343 |
|
| 2012 |
Bivaud S, Balandier JY, Chas M, Allain M, Goeb S, Sallé M. A metal-directed self-assembled electroactive cage with bis(pyrrolo)tetrathiafulvalene (BPTTF) side walls. Journal of the American Chemical Society. 134: 11968-70. PMID 22768798 DOI: 10.1021/Ja305451V |
0.412 |
|
| 2012 |
Goeb S, Bivaud S, Dron PI, Balandier JY, Chas M, Sallé M. A BPTTF-based self-assembled electron-donating triangle capable of C60 binding. Chemical Communications (Cambridge, England). 48: 3106-8. PMID 22344044 DOI: 10.1039/C2Cc00065B |
0.367 |
|
| 2012 |
Wurl A, Goossen S, Canevet D, Sallé M, Pérez EM, Martín N, Klinke C. Supramolecular Interaction of Single-Walled Carbon Nanotubes with a Functional TTF-Based Mediator Probed by Field-Effect Transistor Devices Journal of Physical Chemistry C. 116: 20062-20066. DOI: 10.1021/Jp304970J |
0.727 |
|
| 2012 |
Jia H, Forgie JC, Liu S, Sanguinet L, Levillain E, Le Derf F, Sallé M, Neels A, Skabara PJ, Decurtins S. Tetrathiafulvalene-annulated dipyrrolylquinoxaline: the effect of fluoride on its optical and electrochemical behaviors Tetrahedron. 68: 1590-1594. DOI: 10.1016/J.Tet.2011.11.087 |
0.312 |
|
| 2011 |
Canevet D, Pérez del Pino A, Amabilino DB, Sallé M. Boosting electrical conductivity in a gel-derived material by nanostructuring with trace carbon nanotubes. Nanoscale. 3: 2898-902. PMID 21623428 DOI: 10.1039/C1Nr10235D |
0.702 |
|
| 2011 |
Goeb S, Prusakova V, Wang X, Vézinat A, Sallé M, Castellano FN. Phosphorescent self-assembled Pt(II) tetranuclear metallocycles. Chemical Communications (Cambridge, England). 47: 4397-9. PMID 21373692 DOI: 10.1039/C1Cc10239G |
0.381 |
|
| 2011 |
Hardouin-Lerouge M, Hudhomme P, Sallé M. Molecular clips and tweezers hosting neutral guests. Chemical Society Reviews. 40: 30-43. PMID 21038068 DOI: 10.1039/B915145C |
0.32 |
|
| 2011 |
Zhao B, Zhu X, Peng Q, Yan Z, Derf FL, Sallé M. A novel redox-active calix[4]arene-tetrathiafulvalene dyad Central European Journal of Chemistry. 9: 1102-1108. DOI: 10.2478/S11532-011-0104-9 |
0.355 |
|
| 2011 |
Sallé M, Canevet D, Balandier J, Lyskawa J, Trippé G, Goeb S, Derf FL. Tetrathiafulvalene-Based Architectures: From Guests Recognition to Self-Assembly Phosphorus Sulfur and Silicon and the Related Elements. 186: 1153-1168. DOI: 10.1080/10426507.2010.543099 |
0.73 |
|
| 2011 |
Balandier JY, Chas M, Goeb S, Dron PI, Rondeau D, Belyasmine A, Gallego N, Sallé M. A self-assembled bis(pyrrolo)tetrathiafulvalene-based redox active square New Journal of Chemistry. 35: 165-168. DOI: 10.1039/C0Nj00545B |
0.402 |
|
| 2011 |
Canevet D, Pérez Del Pino A, Amabilino DB, Sallé M. Varied nanostructures from a single multifunctional molecular material Journal of Materials Chemistry. 21: 1428-1437. DOI: 10.1039/C0Jm02302G |
0.731 |
|
| 2011 |
Sauvage J, Trolez Y, Canevet D, Sallé M. Intercalation of Tetrathiafulvalene between the Two Plates of a Copper(I)-Complexed [4]Rotaxane (Eur. J. Org. Chem. 13/2011) European Journal of Organic Chemistry. 2011: n/a-n/a. DOI: 10.1002/Ejoc.201190030 |
0.693 |
|
| 2011 |
Sauvage JP, Trolez Y, Canevet D, Sallé M. Intercalation of tetrathiafulvalene between the two plates of a copper(I)-complexed [4]rotaxane European Journal of Organic Chemistry. 2413-2416. DOI: 10.1002/Ejoc.201100142 |
0.723 |
|
| 2010 |
Balandier JY, Chas M, Dron PI, Goeb S, Canevet D, Belyasmine A, Allain M, Sallé M. N-aryl pyrrolo-tetrathiafulvalene based ligands: synthesis and metal coordination. The Journal of Organic Chemistry. 75: 1589-99. PMID 20143799 DOI: 10.1021/Jo902529E |
0.71 |
|
| 2010 |
Zhao B, Zhou Z, Yan Z, Belhadj E, Derf FL, Sallé M. Synthesis and electrochemical behavior of a model redox-active thiacalix[4]arene-tetrathiafulvalene assembly Tetrahedron Letters. 51: 5815-5818. DOI: 10.1016/J.Tetlet.2010.08.116 |
0.402 |
|
| 2010 |
Lyskawa J, Canevet D, Allain M, Sallé M. An electron-rich three dimensional receptor based on a calixarene- tetrathiafulvalene assembly Tetrahedron Letters. 51: 5868-5872. DOI: 10.1016/J.Tetlet.2010.08.112 |
0.725 |
|
| 2009 |
Canevet D, Sallé M, Zhang G, Zhang D, Zhu D. Tetrathiafulvalene (TTF) derivatives: key building-blocks for switchable processes. Chemical Communications (Cambridge, England). 2245-69. PMID 19377656 DOI: 10.1039/B818607N |
0.726 |
|
| 2008 |
Benhaoua C, Mazari M, Mercier N, Le Derf F, Sallé M. Electrochemical M2+ recognition by an amidopyridyl- tetrathiafulvalene derivative New Journal of Chemistry. 32: 913-916. DOI: 10.1039/B802726A |
0.311 |
|
| 2008 |
Balog M, Rayah H, Derf FL, Sallé M. A versatile building block for EDOT or PEDOT functionalization New Journal of Chemistry. 32: 1183-1188. DOI: 10.1039/B715568A |
0.334 |
|
| 2008 |
Trippé G, Canevet D, Derf FL, Frère P, Sallé M. An extended tetrathiafulvalene redox-ligand incorporating a thiophene spacer Tetrahedron Letters. 49: 5452-5454. DOI: 10.1016/J.Tetlet.2008.07.005 |
0.73 |
|
| 2008 |
Balandier J, Belyasmine A, Sallé M. Tetrathiafulvalene–Imine–Pyridine Assemblies for Pb2+ Recognition European Journal of Organic Chemistry. 2008: 269-276. DOI: 10.1002/Ejoc.200700705 |
0.373 |
|
| 2007 |
Dolder S, Liu SX, Le Derf F, Sallé M, Neels A, Decurtins S. An original redox-responsive ligand based on a pi-extended TTF framework. Organic Letters. 9: 3753-6. PMID 17696357 DOI: 10.1021/Ol7015127 |
0.377 |
|
| 2007 |
Zhao BT, Blesa MJ, Le Derf F, Canevet D, Benhaoua C, Mazari M, Allain M, Sallé M. Carboxylic acid derivatives of tetrathiafulvalene: key intermediates for the synthesis of redox-active calixarene-based anion receptors Tetrahedron. 63: 10768-10777. DOI: 10.1016/J.Tet.2007.06.119 |
0.726 |
|
| 2006 |
Delogu G, Fabbri D, Dettori MA, Sallé M, Derf FL, Blesa MJ, Allain M. Electroactive C(2) symmetry receptors based on the biphenyl scaffold and tetrathiafulvalene units. The Journal of Organic Chemistry. 71: 9096-103. PMID 17109535 DOI: 10.1021/Jo061446M |
0.402 |
|
| 2006 |
Lyskawa J, Sallé M, Balandier JY, Le Derf F, Levillain E, Allain M, Viel P, Palacin S. Monitoring the formation of TTF dimers by Na+ complexation. Chemical Communications (Cambridge, England). 2233-5. PMID 16718313 DOI: 10.1039/B518275A |
0.314 |
|
| 2006 |
Blesa MJ, Zhao BT, Allain M, Le Derf F, Sallé M. Bis(calixcrown)tetrathiafulvalene receptors. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 1906-14. PMID 16419139 DOI: 10.1002/Chem.200500878 |
0.368 |
|
| 2006 |
Hudhomme P, Sallé M, Gautier N, Belyasmine A, Gorgues A. New synthetic routes to highly-extended tetrathiafulvalenes Arkivoc. 2006. DOI: 10.3998/Ark.5550190.0007.406 |
0.326 |
|
| 2006 |
Lyskawa J, Oçafrain M, Trippé G, Derf FL, Sallé M, Viel P, Palacin S. Tetrathiafulvalene-based podands bearing one or two thiol functions: immobilization as self-assembled monolayers or polymer films, and recognition properties Tetrahedron. 62: 4419-4425. DOI: 10.1016/J.Tet.2006.02.054 |
0.364 |
|
| 2006 |
Lyskawa J, Le Derf F, Levillain E, Mazari M, Sallé M. Tetrathiafulvalene-based podands for Pb2+ recognition European Journal of Organic Chemistry. 2322-2328. DOI: 10.1002/Ejoc.200500788 |
0.371 |
|
| 2005 |
Zhao BT, Blesa MJ, Mercier N, Le Derf F, Sallé M. Bis-calix[4]arenes bridged by an electroactive tetrathiafulvalene unit. The Journal of Organic Chemistry. 70: 6254-7. PMID 16050684 DOI: 10.1021/Jo0505876 |
0.33 |
|
| 2005 |
Zhao B, Blesa M, Mercier N, Derf FL, Salle M. A Tetrathiafulvalene-appended Calix[4]arene: Synthesis and Electrochemical Characterization Supramolecular Chemistry. 17: 465-468. DOI: 10.1080/10610270500211743 |
0.331 |
|
| 2005 |
Blesa M-, Zhao B-, Allain M, Mercier N, Sallé M. A Multifunctional Molecular Assembly Associating Tetrathiafulvalene, Calixarene and Crown Ethers Units Phosphorus Sulfur and Silicon and the Related Elements. 180: 1475-1476. DOI: 10.1080/10426500590913195 |
0.341 |
|
| 2005 |
Zhao B, Blesa M, Mercier N, Derf FL, Sallé M. A calixarene-amide-tetrathiafulvalene assembly for the electrochemical detection of anions New Journal of Chemistry. 29: 1164-1167. DOI: 10.1039/B504339E |
0.398 |
|
| 2004 |
Trippé G, Le Derf F, Lyskawa J, Mazari M, Roncali J, Gorgues A, Levillain E, Sallé M. Crown-tetrathiafulvalenes attached to a pyrrole or an EDOT unit: synthesis, electropolymerization and recognition properties. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 6497-509. PMID 15540271 DOI: 10.1002/Chem.200400303 |
0.374 |
|
| 2004 |
Lyskawa J, Le Derf F, Levillain E, Mazari M, Sallé M, Dubois L, Viel P, Bureau C, Palacin S. Univocal demonstration of the electrochemically mediated binding of Pb2+ by a modified surface incorporating a TTF-based redox-switchable ligand. Journal of the American Chemical Society. 126: 12194-5. PMID 15453714 DOI: 10.1021/Ja047411Q |
0.339 |
|
| 2004 |
Derf FL, Trippé G, Benhahoua C, Mazari M, Derdour A, Allain M, Mercier N, Gorgues A, Sallé M. Covalent association of the redox-active TTF framework to N-ligands for the coordination of transition-metal cations Journal De Physique Iv. 114: 573-575. DOI: 10.1051/Jp4:2004114136 |
0.305 |
|
| 2003 |
Migalska-Zalas A, Makowska-Janusik M, Kityk IV, Sahraoui B, Salle M, Gorgues A. Photoinduced SHG in Push-Pull Chromophores 1,3-dithiol-2-yliedene Moieties Embedded in Photopolymer Matrices Acta Physica Polonica A. 103: 293-300. DOI: 10.12693/Aphyspola.103.293 |
0.306 |
|
| 2003 |
Trippé G, Le Derf F, Mazari M, Mercier N, Guilet D, Richomme P, Gorgues A, Becher J, Sallé M. Covalent association of polyaza macrocyclic units to the electroactive tetrathiafulvalene moiety: Synthesis and structural analysis Comptes Rendus Chimie. 6: 573-580. DOI: 10.1016/S1631-0748(03)00084-5 |
0.343 |
|
| 2003 |
Viel P, Palacin S, Descours F, Bureau C, Derf FL, Lyskawa J, Sallé M. Electropolymerized poly-4-vinylpyridine for removal of copper from wastewater Applied Surface Science. 212: 792-796. DOI: 10.1016/S0169-4332(03)00105-3 |
0.319 |
|
| 2002 |
Trippé G, Levillain E, Le Derf F, Gorgues A, Sallé M, Jeppesen JO, Nielsen K, Becher J. Electrochemical recognition of cations by bis(pyrrolo)tetrathiafulvalene macrocycles. Organic Letters. 4: 2461-4. PMID 12123351 DOI: 10.1021/Ol0260829 |
0.373 |
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| 2002 |
Trippé G, Oçafrain M, Besbes M, Monroche V, Lyskawa J, Le Derf F, Sallé M, Becher J, Colonna B, Echegoyen L. Self-assembled monolayers of a tetrathiafulvalene-based redox-switchable ligand New J. Chem.. 26: 1320-1323. DOI: 10.1039/B204996A |
0.389 |
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| 2001 |
Le Derf F, Mazari M, Mercier N, Levillain E, Trippé G, Riou A, Richomme P, Becher J, Garín J, Orduna J, Gallego-Planas N, Gorgues A, Sallé M. Tetrathiafulvalene crowns: redox-switchable ligands. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 447-55. PMID 11271531 DOI: 10.1002/1521-3765(20010119)7:2<447::Aid-Chem447>3.0.Co;2-A |
0.371 |
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| 2001 |
Moreno-Mañas M, Pleixats R, Andreu R, Garín J, Orduna J, Villacampa B, Levillain E, Sallé M. The first 1,3-dithiol-2-ylidene donor–π–acceptor chromophores containing an azine spacer: synthesis, electrochemical and nonlinear optical properties Journal of Materials Chemistry. 11: 374-380. DOI: 10.1039/B007629P |
0.318 |
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| 2001 |
Kityk IV, Sahraoui B, Ledoux-Rak I, Sallé M, Migalska-Zalas A, Kazuo T, Gorgues A. Push–pull chromophores incorporated in 1,3-dithiol-2-ylidene moiety as new electrooptics materials Materials Science and Engineering B-Advanced Functional Solid-State Materials. 87: 148-159. DOI: 10.1016/S0921-5107(01)00714-0 |
0.332 |
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| 2000 |
Terkia-Derdra N, Andreu R, Salle M, Levillain E, Orduna J, Garin J, Orti E, Viruela R, Pou-Amerigo R, Sahraoui B, Gorgues A, Favard JF, Riou A. pi conjugation across the tetrathiafulvalene core: synthesis of extended tetrathiafulvalene derivatives and theoretical analysis of their unusual electrochemical properties Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 1199-213. PMID 10785806 DOI: 10.1002/(Sici)1521-3765(20000403)6:7<1199::Aid-Chem1199>3.3.Co;2-7 |
0.391 |
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| 2000 |
Sahraoui B, Phu XN, Salle M, Cousseau J, Gorgues A. Second Order Hyperpolarisabilities of Various Series of Organic Compounds: Tetrathiafulvalene Derivatives Molecular Crystals and Liquid Crystals. 354: 485-492. DOI: 10.1080/10587250008023642 |
0.332 |
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| 1999 |
Le Derf F, Mazari M, Mercier N, Levillain E, Richomme P, Becher J, Garín J, Orduna J, Gorgues A, Sallé M. Electroregulated Metal-Binding with a Crown Ether Tetrathiafulvalene Derivative: Toward Electrochemically Addressed Metal Cation Sponges. Inorganic Chemistry. 38: 6096-6100. PMID 11671318 DOI: 10.1021/Ic9907617 |
0.323 |
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| 1999 |
Derf FL, Mazari M, Mercier N, Levillain E, Gorgues A, Sallé M, Richomme P, Becher J, Garín J, Orduna J. Thiacrown ether tetrathiafulvalene derivatives as redox responsive ligands Chemical Communications. 1417-1418. DOI: 10.1039/A902497B |
0.363 |
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| 1999 |
Dolbecq A, Guirauden A, Fourmigué M, Boubekeur K, Batail P, Rohmer MM, Bénard M, Coulon C, Sallé M, Blanchard P. Relative basicities of the oxygen atoms of the Linquist polyoxometalate [Mo6O19]2- and their recognition by hydroxyl groups in radical cation salts based on functionalized tetrathiafulvalene π donors Journal of the Chemical Society - Dalton Transactions. 1241-1248. DOI: 10.1039/A809442J |
0.313 |
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| 1999 |
Le Derf F, Sallé M, Mazari M, Mercier N, Riou A, Belyasmine A, Orduna J, Garin J, Becher J, Gorgues A. Electrochemical control of the complexation/expulsion processes of metallic cations by crown ether TTF derivatives Synthetic Metals. 102: 1461. DOI: 10.1016/S0379-6779(98)00529-3 |
0.348 |
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| 1998 |
Nguyen TT, Sallé M, Delaunay J, Riou A, Richomme P, Raimundo JM, Gorgues A, Ledoux I, Dhenaut C, Zyss J, Orduna J, Garín J. Functionalized polyolefinic nonlinear optic chromophores incorporating the 1,3-dithiol-2-ylidene moiety as the electron-donating part Journal of Materials Chemistry. 8: 1185-1192. DOI: 10.1039/A709055B |
0.323 |
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| 1998 |
Andreu R, Barberá J, Garín J, Orduna J, Serrano JL, Sierra T, Leriche P, Sallé M, Riou A, Jubault M, Gorgues A. Synthesis and liquid crystal behaviour of tetrathiafulvalenes containing cyanobiphenylyloxy groups Journal of Materials Chemistry. 8: 881-887. DOI: 10.1039/A708416A |
0.326 |
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| 1998 |
Derf FL, Sallé M, Mazari M, Becher J, Jubault M, Gorgues A, Orduna J, Garín J. New aza-, thia- and oxamacrocyclic tetrathiafulvalene derivatives Synthetic Metals. 94: 49-50. DOI: 10.1016/S0379-6779(97)04140-4 |
0.303 |
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| 1998 |
Sallé M, Bras YL, Andreu R, Leriche P, Mingotaud C, Gorgues A. Use of the cyclodextrin unit for the preparation of Langmuir-Blodgett films of tetrathiafulvalene derivatives Synthetic Metals. 94: 47-48. DOI: 10.1016/S0379-6779(97)04139-8 |
0.319 |
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| 1998 |
Moustarder SL, Hudhomme P, Sallé M, Blanchard P, Riou A, Jubault M, Duguay G, Gorgues A. S-position isomers of BEDT-TTF and derivatives as new precursors of organic materials Synthetic Metals. 94: 41-44. DOI: 10.1016/S0379-6779(97)04137-4 |
0.361 |
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| 1998 |
Derf FL, Sallé M, Mercier N, Becher J, Richomme P, Gorgues A, Orduna J, Garín J. Aza‐Crown Tetrathiafulvalene Derivatives: Synthesis, X‐ray Structure, and Metal Complexation Study European Journal of Organic Chemistry. 1998: 1861-1865. DOI: 10.1002/(Sici)1099-0690(199809)1998:9<1861::Aid-Ejoc1861>3.0.Co;2-L |
0.37 |
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| 1997 |
Bras YL, Sallé M, Leriche P, Mingotaud C, Richomme P, Møller J. Functionalization of the cyclodextrin platform with tetrathiafulvalene units: an efficient access towards redox active Langmuir–Blodgett films Journal of Materials Chemistry. 7: 2393-2396. DOI: 10.1039/A704005I |
0.309 |
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| 1997 |
Ravaine S, Delhaès P, Leriche P, Sallé M. Synthesis of new donor-acceptor systems through the association of a tetrathiafulvalene core and fullerene units Synthetic Metals. 87: 93-95. DOI: 10.1016/S0379-6779(97)80103-8 |
0.426 |
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| 1997 |
Siqot Y, Frère P, Nozdryn T, Cousseau J, Sallé M, Jubault M, Orduna J, Garín J, Gorgues A. Synthesis and electrochemical properties of fused [3,4]furano-tetrathiafulvalenes Tetrahedron Letters. 38: 1919-1922. DOI: 10.1016/S0040-4039(97)00244-X |
0.324 |
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| 1997 |
Leriche P, Belyasmine A, Sallé M, Gorgues A, Jubault M, Garín J, Orduna J. Bis and tetrakis(6-methyl-1,4-dithiafulven-6-yl) substituted tetrathiafulvalenes (TTF) and their vinylogs as novel π-donors Tetrahedron Letters. 38: 1399-1402. DOI: 10.1016/S0040-4039(97)00035-X |
0.345 |
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| 1996 |
Leriche P, Belyasmine A, Sallé M, Frère P, Gorgues A, Riou A, Jubault M, Orduna J, Garín J. Polyacetyl-substituted tetrathiafulvalenes and 1,3-dithiolic derivatives from hex-3-yn-2,5-dione Tetrahedron Letters. 37: 8861-8864. DOI: 10.1016/S0040-4039(96)02063-1 |
0.347 |
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| 1994 |
Gorgues A, Jubault M, Belyasmine A, Salle M, Frere P, Morisson V, Gouriou Y. New Derivatives of Tetrathiafulvalenes (TTF): Towards Organic Metals of Enhanced Dimensionality Phosphorus Sulfur and Silicon and the Related Elements. 95: 235-248. DOI: 10.1080/10426509408034210 |
0.338 |
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| 1993 |
Salle M, Frere P, Gorgues A, Jubault M. Aldehyde Functionalization in the Tetrathiafulvalene Series: Towards New Highly Dimensional Organic Materials Derived from Sulfur-Rich Extended π-Donors Phosphorus Sulfur and Silicon and the Related Elements. 74: 473-474. DOI: 10.1080/10426509308038170 |
0.371 |
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| 1993 |
Salle M, Jubault M, Gorgues A, Boubekeur K, Fourmigue M, Batail P, Canadell E. Bis- and tetrakis(1,4-dithiafulven-6-yl)-substituted tetrathiafulvalenes and dihydrotetrathiafulvalenes: a novel class of planar donor molecules with multiple redox functionalities and the demonstration of a novel type of two-dimensional association in the solid state Chemistry of Materials. 5: 1196-1198. DOI: 10.1021/Cm00033A002 |
0.344 |
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| 1993 |
Salle M, Jubault M, Gorgues A, Cousseau J, Boubekeur K, Fourmigue M, Batail P, Canadell E. Bis and tetrakis (1,4-dithiafulven-6-yl) substituted tetrathiafulvalenes (TTF) and dihyrdro-TTF as precursors of organic metals of enhanced dimensionality Synthetic Metals. 56: 2132-2135. DOI: 10.1016/0379-6779(93)90386-B |
0.347 |
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| 1993 |
Graja A, Salle M, Gorgues A. Infrared spectral properties of cation-radical salts of mono- and bis-hydroxymethyl substituted ethylenedithio-tetrathiafulvalene (TTF) Synthetic Metals. 56: 2118-2123. DOI: 10.1016/0379-6779(93)90383-8 |
0.334 |
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| 1993 |
Blanchard P, Duguay G, Cousseau J, Salle M, Jubault M, Gorgues A, Boubekeur K, Batail P. 2-mono or 2,3-bis(hydroxymethyl)-6,7-ethylenedithio-tetrathiafulvalenes: New potential precursors of organic metals endowed with hydrogen bonds Synthetic Metals. 56: 2113-2117. DOI: 10.1016/0379-6779(93)90382-7 |
0.345 |
|
| 1993 |
Fabre JM, Chakroune S, Giral L, Gorgues A, Salle M. Synthesis and characterization of functionalized unsymmetrically substituted tetrachalcogenofulvalenes Synthetic Metals. 56: 2073-2077. DOI: 10.1016/0379-6779(93)90375-7 |
0.33 |
|
| 1992 |
Blanchard P, Sallé M, Duguay G, Jubault M, Gorgues A. 2-Mono or 2,3-Bis(hydroxymethyl)-6,7-ethylenedithio-tetrathiafulvalenes: New potential precursors of organic metals endowed with hydrogen bonds Tetrahedron Letters. 33: 2685-2688. DOI: 10.1016/S0040-4039(00)79057-5 |
0.357 |
|
| 1992 |
Salle M, Gorgues A, Jubault M, Boubekeur K, Batail P. Tetraformyltetrathiafulvalene (TFTTF) and acetals, precursors of polyfunctionalized TTFs Tetrahedron. 48: 3081-3090. DOI: 10.1016/S0040-4020(01)92250-1 |
0.37 |
|
| 1992 |
Graja A, Yartsev VM, Garrigou-Lagrange C, Sallé M, Gorgues A. Electron-molecular vibration coupling in the cation-radical salt of a giant analogue of TTF with ClO4− anion Physica Status Solidi B-Basic Solid State Physics. 174: 119-128. DOI: 10.1002/Pssb.2221740112 |
0.311 |
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| 1991 |
Salle M, Belyasmine A, Gorgues A, Jubault M, Soyer N. 1,2,4,5-tetrakis-(1,4-dithiafulvalenyl)-benzenes: Aromatic analogs of tetrathiafulvalene Synthetic Metals. 42: 2579-2582. DOI: 10.1016/0379-6779(91)91429-E |
0.386 |
|
| 1991 |
Salle M, Gorgues A, Jubault M, Gouriou Y. A new generation of giant analogs of tetrathiafulvalene (TTF): Bis-and tetrakis-(1,4-dithiafulvalenyl)-TTF Synthetic Metals. 42: 2575-2578. DOI: 10.1016/0379-6779(91)91428-D |
0.341 |
|
| 1991 |
Salle M, Belyasmine A, Gorgues A, Jubault M, Soyer N. Extended analogues of tetrathiafulvalene (TTF): 1,2-bis, 1,4-bis and 1,2,4,5-tetrakis(1,4-dithiafulven-6-yl) benzenes; Synthesis and π-donor abilities. Tetrahedron Letters. 32: 2897-2900. DOI: 10.1016/0040-4039(91)80642-J |
0.358 |
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