Hugues Brisset

Université de Toulon

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Fréderic Fagès

Aix-Marseille Université

Christine Videlot‐Ackermann

Centre Interdisciplinaire de Nanoscience de Marseille

Jean Roncali

Institut des Sciences et Technologies Moléculaires d'Angers

Jörg Ackermann

Centre Interdisciplinaire de Nanoscience de Marseille

Catherine Branger

Université de Toulon

Noriyuki Yoshimoto

Iwate University

Christine Bressy

Université de Toulon

Andrei Sârbu

Institutul Naţional de Cercetare Dezvoltare pentru Chimie si Petrochimie

Y. Didane

Centre National de la Recherche Scientifique

Jean‐Manuel Raimundo

Centre Interdisciplinaire de Nanoscience de Marseille

Cooperative Institutions

Centre National de la Recherche Scientifique

113

Aix-Marseille Université

Centre Interdisciplinaire de Nanoscience de Marseille

Université d'Angers

Université de Toulon

Iwate University

Institutul Naţional de Cercetare Dezvoltare pentru Chimie si Petrochimie

National Institute for Research and Development in Environmental Protection

Matériaux Polymères Interfaces - Environnement Marin

National Institute for Research & Development in Informatics

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Synthesis, electrochemical and photochromic behaviour of a series of (1,4-dithiafulven-6-yl)substituted 3H-naphtho[2,1-b]pyran derivatives

Tetrahedron (2004)

Aude-Emmanuelle Navarro Fabrice Moggia Corinne Moustrou Arnault Heynderickx Fréderic Fagès

Pyran

10.1016/j.tet.2004.10.084

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Citations (17)

The Effect of Monomers on the Recognition Properties of Molecularly Imprinted Beads for Proto-hypericin and Proto-pseudohypericin

Materiale Plastice (2020)

Ana-Mihaela Gavrilă Tanța-Verona Iordache Catherine Branger Hugues Brisset Katri Laatikainen

Molecularly imprinted polymer (MIP) beads for proto-hypericin recognition were prepared by suspension polymerization. In order to study the impact of monomers on the MIPs properties, various monomers such as acrylic acid (AA), hydroxyethyl methacrylate (HEMA), methacrylic acid (MAA) and itaconic acid (IA) in their combinations were crosslinked with ethylene glycol dimethacrylate (EDMA) in the presence of a complex phyto-extract template derived from Hypericum perforatum L. The synthesized MIPs and corresponding non-imprinted polymers NIPs were characterized by infrared spectroscopy analysis, morphology and thermogravimetric analysis. High-performance liquid chromatography combined with UV-Visible spectroscopy, used to investigate the recognition properties of the MIPs for various naphthodianthrones, pointed out that the MIP IA-AA system seemed to be the most adequate for favoring quantitative rebinding of proto-hypericin and proto-pseudohypericin against competitors with similar structures, like hypericin and pseudo-hypericin, which are usually present in high quantities in the primary Hypericum perforatum L. phyto-extracts.

Hypericin

Molecularly imprinted polymer

Ethylene glycol dimethacrylate

10.37358/mp.20.1.5317

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Citations (4)

ChemInform Abstract: Phosphine‐Borane Complexes. Direct Use in Asymmetric Catalysis.

ChemInform (1993)

Hugues Brisset Yann Gourdel Pascal Pellon M. Le Corre

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Boranes

10.1002/chin.199340058

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Citations (0)

Linearly extended hybrid tetrathiafulvalene analogues with bridged dithienylethyleneπ-conjugating spacers

Journal of Materials Chemistry (1997)

Hugues Brisset S. Le Moustarder Philippe Blanchard Bertrand Illien Amédée Riou

New linearly extended π-electron donors based on bridged dithienylethylene (DTE) end-capped with diversely substituted 1,3-dithiol-2-ylidene electron-releasing groups have been synthesized by Wittig–Horner olefination of appropriate aldehydes. Cyclic voltammetry shows that whereas the unbridged analogues are directly oxidized to the dication state through a two-electron transfer, rigidification of the DTE spacer leads to the splitting of the two-electron wave into two successive one-electron steps due to the decrease of the potential corresponding to the formation of the cation radical. This unusual electrochemical behaviour is interpreted with the help of theoretical calculations which suggest that these effects are related to the enhanced electron delocalization resulting from the rigidification of the DTE spacer. This conclusion is supported by an X-ray diffraction structural analysis which reveals that in addition to a fully planar conformation stabilized by intramolecular S‥S interactions, the bridging of the DTE spacer leads to a significant reduction of bond length alternation.

Dication

Tetrathiafulvalene

Electron Delocalization

10.1039/a701463e

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Citations (23)

From organic semiconductors to marine antifouling coatings: how electronic strategies can control bacteria development

HAL (Le Centre pour la Communication Scientifique Directe) (2014)

Christine Bressy Jean‐François Briand Djibril Faye Pierre Frère Frédéric Gohier

Biofouling

Organic semiconductor

Semiconductor Industry

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Electroactive polymers: a new antifouling concept for marine applications

HAL (Le Centre pour la Communication Scientifique Directe) (2014)

Christine Bressy Jean‐François Briand Djibril Faye Brigitte Tanguy Pierre Frère

Biofouling

Source

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Fabrication and characterization of biomimetic textures for antifouling applications

HAL (Le Centre pour la Communication Scientifique Directe) (2019)

Elora Védie Vincent Senez Hugues Brisset Jean‐François Briand Christine Bressy

Biofouling

Characterization

Source

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Functionalization of ‘kite’ shaped styryl end-capped benzodithiophene with ketone groups: synthesis, characterization and properties

Tetrahedron (2011)

Y. Didane Atsufumi Kumagai Noriyuki Yoshimoto Christine Videlot‐Ackermann Hugues Brisset

Surface Modification

10.1016/j.tet.2011.01.006

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Citations (8)

Automated synthesis of new ferrocenyl-modified oligonucleotides: study of their properties in solution

Nucleic Acids Research (2004)

Aude‐Emmanuelle Navarro Nicolas Spinelli Corinne Moustrou Carole Chaix Bernard Mandrand

We have developed new ferrocenyl-modified oligonucleotide (ODN) probes for electrochemical DNA sensors. A monofunctional ferrocene containing phosphoramidite group has been prepared, and a new bisfunctional ferrocene containing phosphoramidite and dimethoxytrityl (DMT) groups has been developed. These ferrocenyl-phosphoramidites have been directly employed in an automated solid-phase DNA synthesizer using phosphoramidite chemistry. The advantages of this method are that it allows a non-specialist in nucleotide chemistry to access labeled ODNs and that it has demonstrated good results. ODNs modified at the 3′ and/or 5′ extremities have been prepared, with the incorporation of the ferrocenyl group into the chain. The 5′ position appears to be more important due to its particular behavior. The thermal stability and electrochemical properties of these new ODN ferrocenes were analyzed before and after hybridization with different ODNs. The feasibility of using these new ferrocenyl-labeled ODNs in DNA sensors has been demonstrated.

Phosphoramidite

Solid-Phase Synthesis

10.1093/nar/gkh874

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Citations (44)

Conjugated linear systems for anti-fouling applications.

HAL (Le Centre pour la Communication Scientifique Directe) (2019)

The Duong Djibril Faye Inmaculada Vieitez Hugues Brisset Pierre Frère

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