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Moltech-Anjou

Séparés par des virgules

Publications

2021

Comparing the self-assembly processes of two redox-active exTTF-based regioisomer Ligands, Dekhtiarenko M., Allain M., Carré V., Aubriet F., Voitenko Z., Sallé M., Goeb S. New J. Chem., 2021, https://doi.org/10.1039/D1NJ04555E

Exciton Coupling in Redox-Active Salen based Self-Assembled Metallacycles, Herasymchuk K., Allain M., MacNeil G. A., Carré V., Aubriet F., Leznoff D. B., Sallé M., Goeb S., Storr T., Chem. Eur. J., 2021, https://doi.org/10.1002/chem.202102745

Reversible pH-Controlled Catenation of a Benzobisimidazole-based Tetranuclear Rectangle, Dekhtiarenko M., Pascal S., Elhabiri M., Mazan V., Canevet D., Allain M., Carré V., Aubriet F., Voitenko Z., Sallé M., Siri O., Goeb S. Chem. Eur. J., 2021, https://doi.org/10.1002/chem.202103039

Azido-perylenediimide: a versatile building block for CuAAC reactions and an alternative precursor for N-annulation, Goujon A., Rocard L., Melnychenko H., Hudhomme P. New J. Chem. 2021. https://doi.org/10.1039/D1NJ02130C

Synthesis and self-assembly of a penta[60]fullerene bearing benzo[ghi]perylenetriimide units, Drou C., Merland, T., Busseau A., Dabos-Seignon S., Goujon A., Hudhomme P., Benyahia L., Chassenieux C., Legoupy S. RSC Advances, 2021. https://doi.org/10.1039/D1RA00287B

Colored Janus Nanocylinders Driven by Supramolecular Coassembly of Donor and Acceptor Building Blocks, Choisnet T., Canevet D., Sallé M., Lorthioir C., Bouteiller L., Woisel P., Niepceron F., Nicol E., Colombani O. ACS Nano, 2021. https://doi.org/10.1021/acsnano.0c07039

Electron-rich Coordination Receptors Based on Tetrathiafulvalene Derivatives: Controlling the Host–Guest Binding, Goeb S., Sallé M. Accounts of Chemical Research, 2021. https://doi.org/10.1021/acs.accounts.0c00828

A self-assembled tetrathiafulvalene box, Krykun S., Croué V., Alévêque O., Levillain E., Allain M., Mézière C., Carré V., Aubriet F., Voïtenko Z., Goeb S., Sallé M. Organic Chemistry Frontiers, 2021. https://doi.org/10.1039/D0QO01543A

2020

Tuning the Organogelating and Spectroscopic Properties of a C3‐Symmetric Pyrene‐Based Gelator through Charge Transfer, Gainar A., Lai T. L.,Oliveras‐González C.,Pop F., Raynal M., Isare B., Bouteiller L., Linares M., Canevet D., Avarvari N., Sallé M., Chemistry an European Journal, 2020. https://doi.org/10.1002/chem.202003914

Side‐chain engineering of perylene diimide dimers: Impact on morphology and photovoltaic performance, Tintori F., Laventure A., El-Berjawi R., Cieplechowicz E., Umer L., Hudhomme P., Welch G. NanoSelect, 2020. https://doi.org/10.1002/nano.202000089

Visible-Light-Mediated Synthesis of AzaBenzannulated Perylenediimide-Based Light-Harvesting Dyads. El-Berjawi R., Rocard L., Goujon A., Cauchy T., Hudhomme P. Journal of Organic Chemistry, 2020. https://doi.org/10.1021/acs.joc.0c01497

Desymmetrization of Perylenediimide Bay‐Regions Using Selective Suzuki‐Miyaura Reactions from Dinitro Substituted Derivatives. Hruzd M., Rocard L., Goujon A., Alain M., Cauchy T., Hudhomme P. Chemistry an European Journal, 2020. in press. https://doi.org/10.1002/chem.202003420 

Tuning the structure and the properties of dithiafulvene metalla-assembled tweezers. Dekhtiarenko M., Krykun S., Carré V., Aubriet F., Canevet D., Allain M., Sallé M., Goeb S., Organic Chemistry Frontiers, 2020, vol 7, n°15, pp.2040-2046, https://doi.org/10.1039/D0QO00641F

 An Imine Photocyclization as an Alternative to the Pictet–Spengler Reaction for the Synthesis of AzaBenzannulated Perylenediimide Dyes. Goujon A., Rocard L., Cauchy T., Hudhomme P., Journal of Organic Chemistry, 2020. https://doi.org/10.1021/acs.joc.0c00600

An original self-assembly using a tetrathiafulvalene-based molecular clip for the recognition of fullerene C60. Cotelle Y., Hardouin-Lerouge M., Lemasson E., Morille Y., Canevet D., Legoupy S., Hudhomme P., Chemical Communications, 2020, vol 56, n°20, pp. 3077-3080. https://doi.org/10.1039/C9CC09633G 

O‐Doped Nanographenes: A Pyrano/Pyrylium Route Towards Semiconducting Cationic Mixed‐Valence Complexes. Ðorđević L., Valentini C., Demitri N., Mézière C., Allain M., Sallé M., Folli A., Murphy D., Mañas‐Valero S., Coronado E., Bonifazi D., Angewandte Chemie International Edition, 2020, vol 59, n°10, pp. 4106-4114. https://doi.org/10.1002/anie.201914025

Metalla-Assembled Electron-Rich Tweezers: Redox-Controlled Guest Release Through Supramolecular Dimerization. Krykun S., Dekhtiarenko M., Canevet D., Carré V., Aubriet F., Levillain E., Allain M., Voitenko Z., Sallé M., Goeb S., Angewandte Chemie International Edition, 2020, vol 59, n°2, pp. 716-720. https://doi.org/10.1002/anie.201912016

Chiral Self-Sorting in Truxene-based Metallacages. Séjourné S., Labrunie A., Dalinot C., Benchohra A., Carré V., Aubriet F., Allain M., Sallé M., Goeb S., Inorganics, 2020, vol 8, n°1, pp. 1. https://doi.org/10.3390/inorganics8010001

Nitro-Perylenediimide: An Emerging Building Block for the Synthesis of Functional Organic Materials. Rocard L., Goujon A., Hudhomme P., Molecules, 2020, vol 25, n°6, pp. 1402. https://doi.org/10.3390/molecules25061402

Comparative whole corona fingerprinting and protein adsorption thermodynamics of PLGA and PCL nanoparticles in human serum. Ndumiso M., Buchtová N., Husselmann L., Mohamed G., Klein A., Aucamp M. E., Canevet D., D’Souza S., Maphasa R. E., Boury F., Dube A. E., Colloids and Surfaces B: Biointerfaces, 2020, vol 188, pp. 110816. https://doi.org/10.1016/j.colsurfb.2020.110816

2019

Recent Developments in the Suzuki–Miyaura Reaction Using Nitroarenes as Electrophilic Coupling Reagents. Rocard L., Hudhomme P., Catalysts, 2019, vol 9, n°3, pp. 213. https://doi.org/10.3390/catal9030213

Original Suzuki-Miyaura Coupling Using Nitro Derivatives for the Synthesis of Perylenediimide-Based Multimers. Rocard L., Hatych D., Chartier T., Cauchy T., Hudhomme P., European Journal of Organic Chemistry, 2019, vol 2019, n°47, pp. 7635-7643. https://doi.org/10.1002/ejoc.201901319

Coordination-driven assembly of a supramolecular square and oxidation to a tetra-ligand radical species. Herasymchuk K., Miller J., Macneil G., Sergeenko A., Mckearney D., Goeb S., Sallé M., Leznoff D., Storr T., Chemical Communications, 2019, vol 55, n°43, pp. 6082-6085. https://doi.org/10.1039/C9CC02320H

Supramolecular chemistry of helical foldamers at the solid–liquid interface: self-assembled monolayers and anion recognition. Adam C., Faour L., Bonnin V., Breton T., Levillain E., Sallé M., Gautier C., Canevet D., Chemical Communications, 2019, vol 55, n°58, pp. 8426-8429. https://doi.org/10.1039/C9CC03851E

Synthesis via direct (hetero)arylation polymerization, electrochemical and optical properties of poly (3,4-disubstituted)thiophenes. Grolleau J., Legoupy S., Frère P., Gohier F., Polymer, 2019, vol 182, pp. 121811. https://doi.org/10.1016/j.polymer.2019.121811

Redox-controlled hybridization of helical foldamers. Faour L., Adam C., Gautier C., Goeb S., Allain M., Levillain E., Canevet D., Sallé M., Chemical Communications, 2019, vol 55, n°40, pp. 5743-5746. https://doi.org/10.1039/C9CC02498K

Robust supramolecular nanocylinders of naphthalene diimide in water. Choisnet T., Canevet D., Sallé M., Nicol E., Niepceron F., Jestin J., Colombani O., Chemical Communications, 2019, vol 55, n°64, pp. 9519-9522. https://doi.org/10.1039/C9CC04723A

2018

Redox-Driven Transformation of a Discrete Molecular Cage into an Infinite 3D Coordination Polymer. Szalóki G., Krykun S., Croué V., Allain M., Morille Y., Aubriet F., Carré V., Voitenko Z., Goeb S., Sallé M., Chemistry - A European Journal, 2018, vol 24, n°44, pp. 11273-11277. https://doi.org/10.1002/chem.201801653

New insights into polymer solar cells stability: The crucial role of PCBM oxidation. Perthué A., Gorisse T., Silva H. S., Lombard C., Bégué D., Hudhomme P., Pepin-Donat B., Rivaton A., Wantz G., Journal of Materials Research, 2018, vol 33, n°13, pp. 1868-1878. https://doi.org/10.1557/jmr.2018.141

(Super)Gelators derived from push-pull chromophores: Synthesis, gelling properties and second harmonic generation. Marco A.-B., Gindre D., Iliopoulos K., Franco S., Andreu R., Canevet D., Sallé M., Organic and Biomolecular Chemistry, 2018, vol 16, pp. 2470-2478. https://doi.org/10.1039/C8OB00251G

Triphenylamine-Based Push–Pull σ–C60 Dyad As Photoactive Molecular Material for Single-Component Organic Solar Cells: Synthesis, Characterizations, and Photophysical Properties. Labrunie A., Gorenflot J., Babics M., Alévêque O., Dabos-Seignon S., Balawi A., Kan Z., Wohlfahrt M., Levillain E., Hudhomme P., Beaujuge P., Laquai F., Cabanetos C., Blanchard P., Chemistry of Materials, 2018, vol 30, n°10, pp. 3474-3485. https://doi.org/10.1021/acs.chemmater.8b01117

Tuning the electronic properties and the planarity degree in the π-extended TTF series: the prominent role of heteroatoms. Krykun S., Croué V., Allain M., Voitenko Z., Arago J., Ortí E., Goeb S., Sallé M., Journal of Materials Chemistry C, 2018, vol 6, n°48, pp. 13190-13196. https://doi.org/10.1039/C8TC04730H

A M2L2 Redox-Active Metalla-Macrocycle Based on Electron-Rich 9-(1,3-Dithiol-2-ylidene)Fluorene. Krykun S., Allain M., Carré V., Aubriet F., Voitenko Z., Goeb S., Sallé M., Inorganics, 2018, vol 6, n°2, pp. 44. https://doi.org/10.3390/inorganics6020044

Functionalised tetrathiafulvalene- (TTF-) macrocycles: recent trends in applied supramolecular chemistry. Jana A., Bähring S., Ishida M., Canevet D., Jeppesen J., Sessler J., Herasymchuk K., Miller J., Macneil G., Sergeenko A., Mckearney D., Goeb S., Sallé M., Leznoff D., Storr T., Chemical Society Reviews, 2018, vol 47, n°15, pp. 5614-5645. https://doi.org/10.1039/C8CS00035B

Synthesis of a perylenediimide-fullerene C60 dyad: A simple use of a nitro leaving group for a Suzuki-Miyaura coupling reaction. El-Berjawi R., Hudhomme P., Dyes and Pigments, 2018, vol 159, pp. 551-556. https://doi.org/10.1016/j.dyepig.2018.07.037

Pyrene-functionalized Foldamer: Structural Impact and Recognition Properties supported by Donor-Acceptor Interactions. Aparicio F., Faour L., Allain M., Canevet D., Sallé M., Chemical Communications, 2017, vol 53, n°88, pp. 12028-12031. https://doi.org/10.1039/C7CC07253H

Self-Assembled Cofacial Zinc-Porphyrin Supramolecular Nanocapsules as Tuneable 1O2 Photosensitizers. Colomban C., Fuertes-Espinosa C., Goeb S., Sallé M., Costas M., Blancafort L., Ribas X., Chemistry - A European Journal, 2018, vol 24, n°17, pp. 4371-4381. https://doi.org/10.1002/chem.201705531

Enhanced Penta(organo)[60]fullerenes by Electroactive Donor Units for Supramolecular Polymers. Busseau A., Villegas C., Dabos-Seignon S., Hudhomme P., Legoupy S., European Journal of Organic Chemistry, 2018, n°35, pp. 4860-4866. https://doi.org/10.1002/ejoc.201801042

2017

Rapid and green synthesis of complementary D-A small molecules for organic photovoltaics. Grolleau J., Gohier F., Allain M., Legoupy S., Cabanetos C., Frère P., Organic Electronics, 2017, vol 42, pp. 322-328. https://doi.org/10.1016/j.orgel.2016.12.046

Toward sustainable organic semiconductors from a broad palette of green reactions. Faurie A., Grolleau J., Gohier F., Allain M., Legoupy S., Frère P., European Journal of Organic Chemistry, 2017, vol 2017, n°19, pp. 2707-2714. https://doi.org/10.1002/ejoc.201700317

Controlling the Host-Guest Interaction Mode through a Redox Stimulus. Szalóki G., Croué V., Carré V., Aubriet F., Alévêque O., Levillain E., Allain M., Aragó J., Ortí E., Goeb S., Sallé M., Angewandte Chemie International Edition, 2017, vol 56, n°51, pp. 16272-16276. https://doi.org/10.1002/anie.201709483

A self-assembled M2L4 cage incorporating electron-rich 9-(1,3-dithiol-2-ylidene)fluorene units. Croué V., Krykun S., Allain M., Morille Y., Aubriet F., Carré V., Voitenko Z., Goeb S., Sallé M., New Journal of Chemistry, 2017, vol 41, n°9, pp. 3238-3241. https://doi.org/10.1039/C7NJ00062F

Reversible C60 Ejection from a Metallocage through the Redox-Dependent Binding of a Competitive Guest. Colomban C., Szalóki G., Allain M., Gomez L., Goeb S., Sallé M., Costas M., Ribas X., Chemistry - A European Journal, 2017, vol 23, n°13, pp. 3016-3022. https://doi.org/10.1002/chem.201700273

Absorption Spectroelectrochemistry on Mixed Perylenediimide-Based Self-Assembled Monolayers: Non-Linear Dependence of Absorbance versus Surface Coverage. Bkhach S., Alévêque O., Morille Y., Breton T., Hudhomme P., Gautier C., Levillain E., ChemElectroChem, 2017, vol 4, n°3, pp. 601-606. https://doi.org/10.1002/celc.201600770

Coordination entities of a Pyrene-based Iminopyridine ligand: Structural and photophysical properties. Ayadi A., Branzea D.-G., Allain M., Canevet D., Dincalp H., El-Ghayoury A., Polyhedron, 2017, vol 135, pp. 86-95. https://doi.org/10.1016/j.poly.2017.07.001

2016

Ionic liquid supported organotin reagents to prepare molecular imaging and therapy agents. Rajerison H., Faye D., Roumesy A., Louaisil N., Boeda F., Faivre-Chauvet A., Gestin J.-F., Legoupy S., Organic and Biomolecular Chemistry, 2016, vol 14, pp. 2121-2126. Réf. HAL: inserm-01280171

Highly stable perylenediimide based self-assembled monolayers studied by spectroelectrochemistry. Levillain E., Bkhach S., Le Duc Y., Alévêque O., Gautier C., Hudhomme P., ChemElectroChem, 2016, pp. 887-891. Réf. HAL: hal-01388823

New Penta(tetrathiafulvalenyl)[60]fullerenes for Supramolecular Materials. Busseau A., Villegas C., Dabos-Seignon S., Cabanetos C., Hudhomme P., Legoupy S., Chemistry - A European Journal, 2016, vol 22, n°25, pp. 8452-8456. Réf. HAL: hal-02888811

Preparation of a tetrahydroxyphenazine-modified carbon as cathode material for supercapacitor in aqueous acid electrolyte.Legoupy S., Lebegue E., Cougnon C., Electrochemistry Communications, 2016, vol 70, pp. 47-50. Réf. HAL: hal-02868523

Neutral versus polycationic coordination cages: a comparison regarding neutral guest inclusion. Szalóki G., Croué V., Allain M., Goeb S., Sallé M., Chemical Communications, 2016, vol 52, n°65. Réf. HAL: hal-01416415

Triggering Gel Formation and Luminescence through Donor-Acceptor Interactions in a C 3-Symmetric Tris(pyrene) System. Lai T.-L., Pop F., Melan C., Canevet D., Sallé M., Avarvari N., Chemistry - A European Journal, 2016, vol 22, n°17, pp. 5839-5843. Réf. HAL: hal-02913734

Internal Probing of the Supramolecular Organization of Pyrene-Based Organogelators. Lai T.-L., Canevet D., Avarvari N., Sallé M., Chemistry - An Asian Journal, 2016, vol 11, n°1, pp. 81-85. Réf. HAL: hal-02913732

Promoting Spontaneous Second Harmonic Generation through Organogelation. Marco A.-B., Aparicio F., Faour L., Iliopoulos K., Morille Y., Allain M., Franco S., Andreu R., Sahraoui B., Gindre D., Canevet D., Sallé M., Journal of the American Chemical Society, 2016, vol 138, n°29, pp. 9025-9028. Réf. HAL: hal-01391731

Syntheses via a direct arylation method of push-​pull molecules based on triphenylamine and 3-​cyano-​4-​hexyloxythiophene moieties. Grolleau J., Gohier F., Cabanetos C., Allain M., Legoupy S., Frère P., Organic and Biomolecular Chemistry, 2016, vol 14, n°44, pp. 10516-10522. Réf. HAL: hal-01447587

Reversible Guest Uptake/Release by Redox-Controlled Assembly/Disassembly of a Coordination Cage. Croué V., Goeb S., Szalóki G., Allain M., Sallé M., Angewandte Chemie International Edition, 2016, vol 55, n°5. HAL: hal-01416401

Coumarin-Containing Polymers for High Density Non-Linear Optical Data Storage. Gindre D., Iliopoulos K., Krupka O., Evrard M., Champigny E., Sallé M., Molecules, 2016, vol 21, n°2, pp. 147. Réf. HAL: hal-01391727

C60 Recognition from Extended Tetrathiafulvalene Bis-acetylide Platinum(II) Complexes. Bastien G., Dron P.-I., Vincent M., Canevet D., Allain M., Goeb S., Sallé M., Organic Letters, 2016, vol 18, n°22, pp. 5856-5859. Réf. HAL: hal-01393747

Supramolecular Control over the Structural Organization of a Second-Order NLO-active Organogelator. Aparicio F., Faour L., Gindre D., Canevet D., Sallé M., Soft Matter, 2016, pp. 8480-8484. Réf. HAL: hal-01391734

2015

Synthesis, spectroscopic and electrochemical properties of new covalent assemblies between TTF and various acceptors. Zitouni A., Hamel A., Bouguessa S., Gouasmia A., El-Ghayoury A., Frère P., Sallé M., Synthetic Metals, 2015, vol 204, pp. 84-89. Réf. HAL: hal-01390949

Anionic polymerization by an electron transfer process from a CdSe quantum dot–perylenediimide (PDI) system. Rusen E., Mocanu A., Nistor L., Hudhomme P., Diacon A., RSC Advances, 2015, vol 5, n°36, pp. 28228-28232. Réf. HAL: hal-01390959

Synthesis of Novel Triazolo Cyclobutane Nucleoside Analogs. Ngo N., Tran T., Dinh T., Vo-Thanh G., Legoupy S., Bulletin of the Korean Chemical Society, 2015, vol 36, n°5, pp. 1390-1395. Réf. HAL: hal-01308807

Metal-driven Self-Assembly: the Case of Redox-Active Discrete Architectures. Croué V., Goeb S., Sallé M., Chemical Communications, 2015, pp. 7263-7406. Réf. HAL: hal-01390940

Glycoluril–tetrathiafulvalene molecular clips: on the influence of electronic and spatial properties for binding neutral accepting guests. Cotelle Y., Hardouin-Lerouge M., Legoupy S., Alévêque O., Levillain E., Hudhomme P., Beilstein Journal of Organic Chemistry, 2015, vol 11, n°1023-1036, pp. 1023-1036. Réf. HAL: hal-01301844

Tuning the size of a redox-active tetrathiafulvalene-based self-assembled ring. Bivaud S., Goeb S., Croué V., Allain M., Pop F., Sallé M., Beilstein Journal of Organic Chemistry, 2015, vol 11, pp. 966-971. Réf. HAL: hal-01391706

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