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Vidal, N., Cavaille, J. P., Graziani, F., Robin, M., Ouari, O., Pietri, S., & Stocker, P. (2014). High throughput assay for evaluation of reactive carbonyl scavenging capacity. Redox Biology, 2, 590–598. https://doi.org/10.1016/j.redox.2014.01.016
Audran, G., Bremond, P., & Marque, S. R. A. (2014). Labile alkoxyamines: past, present, and future. Chemical Communications, 50(59), 7921–7928. https://doi.org/10.1039/c4cc01364f
Thureau, P., Mollica, G., Ziarelli, F., & Viel, S. (2014). Solid-State H-1 NMR Studies of Homonuclear Dipolar Couplings. Annual Reports on Nmr Spectroscopy, Vol 82, 82, 217–249. https://doi.org/10.1016/B978-0-12-800184-4.00005-9
Lelli, M., Rossini, A. J., Casano, G., Ouari, O., Tordo, P., Lesage, A., & Emsley, L. (2014). Hydrophobic radicals embedded in neutral surfactants for dynamic nuclear polarization of aqueous environments at 9.4 Tesla. Chemical Communications, 50(71), 10198–10201. https://doi.org/10.1039/c4cc02152e
Chalier, F., Clement, J.-L., Hardy, M., Tordo, P., & Rockenbauer, A. (2014). ESR study of the spin adducts of three analogues of DEPMPO substituted at C-4 or C-3. Rsc Advances, 4(23), 11610–11623. https://doi.org/10.1039/c3ra46913a
Bardelang, D., Brinkmann, A., Ratcliffe, C. I., Ripmeester, J. A., Terskikh, V. V., & Udachin, K. A. (2014). High field solid state C-13 NMR spectroscopy of cucurbituril materials. Crystengcomm, 16(18), 3788–3795. https://doi.org/10.1039/c3ce42467g
Vibert, F., Marque, S. R. A., Bloch, E., Queyroy, S., Bertrand, M. P., Gastaldi, S., & Besson, E. (2014). Arylsulfanyl radical lifetime in nanostructured silica: dramatic effect of the organic monolayer structure. Chemical Science, 5(12), 4716–4723. https://doi.org/10.1039/c4sc01907e
Le Breton, N., Martinho, M., Kabytaev, K., Topin, J., Mileo, E., Blocquel, D., Habchi, J., Longhi, S., Rockenbauer, A., Golebiowski, J., Guigliarelli, B., Marque, S. R. A., & Belle, V. (2014). Diversification of EPR signatures in site directed spin labeling using a beta-phosphorylated nitroxide. Physical Chemistry Chemical Physics, 16(9), 4202–4209. https://doi.org/10.1039/c3cp54816c
Ziarelli, F., Casciola, M., Pica, M., Donnadio, A., Aussenac, F., Sauvee, C., Capitani, D., & Viel, S. (2014). Dynamic nuclear polarisation NMR of nanosized zirconium phosphate polymer fillers. Chemical Communications, 50(70), 10137–10139. https://doi.org/10.1039/c4cc02723j
Detrembleur, C., Jerome, C., De Winter, J., Gerbaux, P., Clement, J.-L., Guillaneuf, Y., & Gigmes, D. (2014). Nitroxide mediated polymerization of methacrylates at moderate temperature. Polymer Chemistry, 5(2), 335–340. https://doi.org/10.1039/c3py01133j
Trimaille, T., Autissier, L., Rakotonirina, M. D., Guillaneuf, Y., Villard, C., Bertin, D., Gigmes, D., & Mabrouk, K. (2014). Peptide ligation from alkoxyamine based radical addition. Chemical Communications, 50(21), 2744–2747. https://doi.org/10.1039/c3cc49389j
Drujon, J., Rahmani, R., Héran, V., Blanc, R., Carissan, Y., Tuccio, B., Commeiras, L., & Parrain, J.-L. (2014). trans-1,2-Disiloxybenzocyclobutene, an adequate partner for the auto-oxidation: EPR/spin trapping and theoretical studies. Physical Chemistry Chemical Physics, 16(16), 7513. https://doi.org/10.1039/c3cp55077j
Pertici, V., Trimaille, T., Laurin, J., Felix, M.-S., Marqueste, T., Pettmann, B., Chauvin, J.-P., Gigmes, D., & Decherchi, P. (2014). Repair of the injured spinal cord by implantation of a synthetic degradable block copolymer in rat. Biomaterials, 35(24), 6248–6258. https://doi.org/10.1016/j.biomaterials.2014.04.020
Xiao, P., Dumur, F., Frigoli, M., Graff, B., Morlet-Savary, F., Wantz, G., Bock, H., Fouassier, J. P., Gigmes, D., & Lalevée, J. (2014). Perylene derivatives as photoinitiators in blue light sensitive cationic or radical curable films and panchromatic thiol-ene polymerizable films. European Polymer Journal, 53, 215–222. https://doi.org/10.1016/j.eurpolymj.2014.01.024
Dumur, F., Lepeltier, M., Siboni, H. Z., Gigmes, D., & Aziz, H. (2014). Phosphorescent organic light-emitting devices (PhOLEDs) based on heteroleptic bis-cyclometalated complexes using acetylacetonate as the ancillary ligand. Synthetic Metals, 198, 131–136. https://doi.org/10.1016/j.synthmet.2014.09.026
Dumur, F., Lepeltier, M., Zamani Siboni, H., Xiao, P., Graff, B., Lalevée, J., Gigmes, D., & Aziz, H. (2014). Concentration-insensitive phosphorescent organic light emitting devices (PhOLEDs) for easy manufacturing. Journal of Luminescence, 151, 34–40. https://doi.org/10.1016/j.jlumin.2014.01.073
Mokbel, H., Dumur, F., Mayer, C. R., Morlet-Savary, F., Graff, B., Gigmes, D., Toufaily, J., Hamieh, T., Fouassier, J.-P., & Lalevée, J. (2014). End capped polyenic structures as visible light sensitive photoinitiators for polymerization of vinylethers. Dyes and Pigments, 105, 121–129. https://doi.org/10.1016/j.dyepig.2014.02.002
Dumur, F., Beouch, L., Tehfe, M.-A., Contal, E., Lepeltier, M., Wantz, G., Graff, B., Goubard, F., Mayer, C. R., Lalevée, J., & Gigmes, D. (2014). Low-cost zinc complexes for white organic light-emitting devices. Thin Solid Films, 564, 351–360. https://doi.org/10.1016/j.tsf.2014.06.006
Dumur, F., Lepeltier, M., Siboni, H. Z., Xiao, P., Graff, B., Lalevée, J., Gigmes, D., & Aziz, H. (2014). Pure red phosphorescent OLED (PhOLED) based on a cyclometalated iridium complex with a dibenzoylmethane (dbm) moiety as the ancillary ligand. Thin Solid Films, 562, 530–537. https://doi.org/10.1016/j.tsf.2014.04.096
Gaucher-Wieczorek, F., Guérineau, V., Touboul, D., Thétiot-Laurent, S., Pelissier, F., Badet-Denisot, M.-A., Badet, B., & Durand, P. (2014). Evaluation of synthase and hemisynthase activities of glucosamine-6-phosphate synthase by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Analytical Biochemistry, 458, 61–65. https://doi.org/10.1016/j.ab.2014.04.033
Lê, D., Liénafa, L., Phan, T. N. T., Deleruyelle, D., Bouchet, R., Maria, S., Bertin, D., & Gigmes, D. (2014). Photo-Cross-Linked Diblock Copolymer Micelles: Quantitative Study of Photochemical Efficiency, Micelles Morphologies and their Thermal Behavior. Macromolecules, 47(7), 2420–2429. https://doi.org/10.1021/ma5000656
Xiao, P., Dumur, F., Graff, B., Morlet-Savary, F., Gigmes, D., Fouassier, J. P., & Lalevée, J. (2014). Design of High Performance Photoinitiators at 385–405 nm: Search around the Naphthalene Scaffold. Macromolecules, 47(3), 973–978. https://doi.org/10.1021/ma402622v
Xiao, P., Hong, W., Li, Y., Dumur, F., Graff, B., Fouassier, J. P., Gigmes, D., & Lalevée, J. (2014). Diketopyrrolopyrrole dyes: Structure/reactivity/efficiency relationship in photoinitiating systems upon visible lights. Polymer, 55(3), 746–751. https://doi.org/10.1016/j.polymer.2014.01.003
Zhang, J., Frigoli, M., Dumur, F., Xiao, P., Ronchi, L., Graff, B., Morlet-Savary, F., Fouassier, J. P., Gigmes, D., & Lalevée, J. (2014). Design of Novel Photoinitiators for Radical and Cationic Photopolymerizations under Near UV and Visible LEDs (385, 395, and 405 nm). Macromolecules, 47(9), 2811–2819. https://doi.org/10.1021/ma500612x
Tehfe, M.-A., Dumur, F., Xiao, P., Zhang, J., Graff, B., Morlet-Savary, F., Gigmes, D., Fouassier, J.-P., & Lalevée, J. (2014). Photoinitiators based on a phenazine scaffold: High performance systems upon near-UV or visible LED (385, 395 and 405 nm) irradiations. Polymer, 55(10), 2285–2293. https://doi.org/10.1016/j.polymer.2014.04.005
Zhang, J., Zivic, N., Dumur, F., Xiao, P., Graff, B., Fouassier, J. P., Gigmes, D., & Lalevée, J. (2014). UV-violet-blue LED induced polymerizations: Specific photoinitiating systems at 365, 385, 395 and 405 nm. Polymer, 55(26), 6641–6648. https://doi.org/10.1016/j.polymer.2014.11.002
Mlayah-Bellalouna, S., Dufour, M., Mabrouk, K., Mejdoub, H., Carlier, E., Othman, H., Belghazi, M., Tarbe, M., Goaillard, J. M., Gigmes, D., Seagar, M., El Ayeb, M., Debanne, D., & Srairi-Abid, N. (2014). AaTX1, from Androctonus australis scorpion venom: Purification, synthesis and characterization in dopaminergic neurons. Toxicon, 92, 14–23. https://doi.org/10.1016/j.toxicon.2014.09.005
Obadia, M. M., Mudraboyina, B. P., Serghei, A., Phan, T. N. T., Gigmes, D., & Drockenmuller, E. (2014). Enhancing Properties of Anionic Poly(ionic liquid)s with 1,2,3-Triazolium Counter Cations. ACS Macro Letters, 3(7), 658–662. https://doi.org/10.1021/mz500310j
Xiao, P., Dumur, F., Zhang, J., Fouassier, J. P., Gigmes, D., & Lalevée, J. (2014). Copper Complexes in Radical Photoinitiating Systems: Applications to Free Radical and Cationic Polymerization upon Visible LEDs. Macromolecules, 47(12), 3837–3844. https://doi.org/10.1021/ma5006793
Le, D., Casano, G., Phan, T. N. T., Ziarelli, F., Ouari, O., Aussenac, F., Thureau, P., Mollica, G., Gigmes, D., Tordo, P., & Viel, S. (2014). Optimizing Sample Preparation Methods for Dynamic Nuclear Polarization Solid-state NMR of Synthetic Polymers. Macromolecules, 47(12), 3909–3916. https://doi.org/10.1021/ma500788n
d’Ayala, G. G., Malinconico, M., Laurienzo, P., Tardy, A., Guillaneuf, Y., Lansalot, M., D’Agosto, F., & Charleux, B. (2014). RAFT/MADIX Copolymerization of Vinyl Acetate and 5,6-Benzo-2-methylene-1,3-dioxepane. Journal of Polymer Science Part A-Polymer Chemistry, 52(1), 104–111. https://doi.org/10.1002/pola.26976
Broggi, J., Terme, T., & Vanelle, P. (2014). Organic Electron Donors as Powerful Single-Electron Reducing Agents in Organic Synthesis. Angewandte Chemie-International Edition, 53(2), 384–413. https://doi.org/10.1002/anie.201209060
Biver, E., Berta, M., D’Aléo, A., Phan, T., Maria, S., Fages, F., Gigmes, D., Sentis, M., & Delaporte, P. (2014). Influence of Pyrene Grafting on PMMA Nanosecond Laser Ablation at 248 nm. ACS Applied Materials & Interfaces, 6(1), 41–48. https://doi.org/10.1021/am404376e
Mayeux, C., Massi, L., Gal, J.-F., Charles, L., & Burk, P. (2014). Catalytic Effect of Cesium Cation Adduct Formation on the Decarboxylation of Carboxylate Ions in the Gas Phase. Chemistry-a European Journal, 20(3), 815–823. https://doi.org/10.1002/chem.201303669
Xiao, P., Frigoli, M., Dumur, F., Graff, B., Gigmes, D., Fouassier, J. P., & Lalevée, J. (2014). Julolidine or Fluorenone Based Push–Pull Dyes for Polymerization upon Soft Polychromatic Visible Light or Green Light. Macromolecules, 47(1), 106–112. https://doi.org/10.1021/ma402196p
Xiao, P., Dumur, F., Graff, B., Morlet-Savary, F., Vidal, L., Gigmes, D., Fouassier, J. P., & Lalevée, J. (2014). Structural Effects in the Indanedione Skeleton for the Design of Low Intensity 300–500 nm Light Sensitive Initiators. Macromolecules, 47(1), 26–34. https://doi.org/10.1021/ma402149g
Tintaru, A., Chendo, C., Wang, Q., Viel, S., Quelever, G., Peng, L., Posocco, P., Pricl, S., & Charles, L. (2014). Conformational sensitivity of conjugated poly(ethylene oxide)-poly(amidoamine) molecules to cations adducted upon electrospray ionization - A mass spectrometry, ion mobility and molecular modeling study. Analytica Chimica Acta, 808, 163–174. https://doi.org/10.1016/j.aca.2013.08.030
Lorion, C., Faye, C., Maret, B., Trimaille, T., Regnier, T., Sommer, P., & Debret, R. (2014). Biosynthetic support based on dendritic poly(L-lysine) improves human skin fibroblasts attachment. Journal of Biomaterials Science-Polymer Edition, 25(2), 136–149. https://doi.org/10.1080/09205063.2013.843966
Oliver, J. D., Rosser, A. A., Fellows, C. M., Guillaneuf, Y., Clement, J.-L., Gaborieau, M., & Castignolles, P. (2014). Understanding and improving direct UV detection of monosaccharides and disaccharides in free solution capillary electrophoresis. Analytica Chimica Acta, 809, 183–193. https://doi.org/10.1016/j.aca.2013.12.001
Xiao, P., Dumur, F., Graff, B., Gigmes, D., Fouassier, J. P., & Lalevée, J. (2014). Blue Light Sensitive Dyes for Various Photopolymerization Reactions: Naphthalimide and Naphthalic Anhydride Derivatives. Macromolecules, 47(2), 601–608. https://doi.org/10.1021/ma402376x
Beziere, N., Hardy, M., Poulhes, F., Karoui, H., Tordo, P., Ouari, O., Frapart, Y.-M., Rockenbauer, A., Boucher, J.-L., Mansuy, D., & Peyrot, F. (2014). Metabolic stability of superoxide adducts derived from newly developed cyclic nitrone spin traps. Free Radical Biology and Medicine, 67, 150–158. https://doi.org/10.1016/j.freeradbiomed.2013.10.812
Bardelang, D., Giorgi, M., Hornebecq, V., Stepanov, A., Hardy, M., Rizzato, E., Monnier, V., Zaman, M. B., Chan, G., Udachin, K., Enright, G., Tordo, P., & Ouari, O. (2014). Hosting Various Guests Including Fullerenes and Free Radicals in Versatile Organic Paramagnetic bTbk Open Frameworks. Crystal Growth & Design, 14(2), 467–476. https://doi.org/10.1021/cg401097e
Delplace, V., Harrisson, S., Tardy, A., Gigmes, D., Guillaneuf, Y., & Nicolas, J. (2014). Nitroxide-Mediated Radical Ring-Opening Copolymerization: Chain-End Investigation and Block Copolymer Synthesis. Macromolecular Rapid Communications, 35(4), 484–491. https://doi.org/10.1002/marc.201300809
Primas, N., Neilde, K., Kabri, Y., Crozet, M. D., Terme, T., & Vanelle, P. (2014). Exploring the Synthesis and the Reactivity of 4-[4-(Chloromethyl) styryl]-1,2-dimethyl-5-nitro-1H-imidazole in TDAE Strategy. Synthesis-Stuttgart, 46(3), 348–356. https://doi.org/10.1055/s-0033-1338572
Geetha, K., Umadevi, M., Sathe, G. V., Vanelle, P., Terme, T., & Khoumeri, O. (2014). Orientation of 1,4-dimethoxy-3-bromomethylanthracence-9,10-dione on silver nanoparticles: SERS studies. Journal of Molecular Structure, 1059, 87–93. https://doi.org/10.1016/j.molstruc.2013.11.013
Le Lamer, S., Paradis, S., Rahmouni, H., Chaimbault, C., Michaud, M., Culcasi, M., Afxantidis, J., Latreille, M., Berna, P., Berdeaux, A., Pietri, S., Morin, D., Donazzolo, Y., Abitbol, J.-L., Pruss, R. M., & Schaller, S. (2014). Translation of TRO40303 from myocardial infarction models to demonstration of safety and tolerance in a randomized Phase I trial. Journal of Translational Medicine, 12, 38. https://doi.org/10.1186/1479-5876-12-38
Audran, G., Bremond, P., Franconi, J.-M., Marque, S. R. A., Massot, P., Mellet, P., Parzy, E., & Thiaudiere, E. (2014). Alkoxyamines: a new family of pro-drugs against cancer. Concept for theranostics. Organic & Biomolecular Chemistry, 12(5), 719–723. https://doi.org/10.1039/c3ob42076k
Dumur, F., Lepeltier, M., Siboni, H. Z., Gigmes, D., & Aziz, H. (2014). Highly Efficient Organic Light-Emitting Devices Prepared with a Phosphorescent Heteroleptic Iridium (III) Complex Containing 7,8-Benzoquinoline as the Cyclometalated Ligand. Advanced Optical Materials, 2(3), 262–266. https://doi.org/10.1002/adom.201300437
Benmohammed, A., Khoumeri, O., Djafri, A., Terme, T., & Vanelle, P. (2014). Synthesis of Novel Highly Functionalized 4-Thiazolidinone Derivatives from 4-Phenyl-3-thiosemicarbazones. Molecules, 19(3), 3068–3083. https://doi.org/10.3390/molecules19033068