Pertici, V., Martrou, G., Gigmes, D., & Trimaille, T. (2018). Synthetic Polymer-based Electrospun Fibers: Biofunctionalization Strategies and Recent Advances in Tissue Engineering, Drug Delivery and Diagnostics. Current Medicinal Chemistry, 25(20), 2385–2400. https://doi.org/10.2174/0929867325666171129133120
Benlarbi, F., Stoker, P., & Yousfi, M. (2018). Investigation of antioxidant and antihemolytic activities of Algerian defatted olive fruits (olea europaea L.) at two ripening stages. Mediterranean Journal of Nutrition and Metabolism, 11(3), 217–233. https://doi.org/10.3233/MNM-17187
Edeleva, M. V., Marque, S., & Bagryanskaya, E. G. (2018). Imidazoline and imidazolidine nitroxides as controlling agents in nitroxide-mediated pseudoliving radical polymerization. Russian Chemical Reviews, 87(4), 328–349. https://doi.org/10.1070/RCR4765
Casano, G., Karoui, H., & Ouari, O. (2018). Polarizing Agents: Evolution and Outlook in Free Radical Development for DNP. Emagres, 7(4), 195–207. https://doi.org/10.1002/9780470034590.emrstm1547
Morris, J. C., Clement, J.-L., Guillaneuf, Y., Bottle, S. E., Fairfull-Smith, K., & Gigmes, D. (2018). Reducing the Hydrogen Atom Abstraction Efficiencies of Benzophenone-Based Photosensitive Alkoxyamines. In K. Matyjaszewski, H. Gao, B. S. Sumerlin, & N. V. Tsarevsky (Eds.), Reversible Deactivation Radical Polymerization, Vol 2: Mechanisms and Synthetic Methodologies (Vol. 1284, pp. 105–133).
Haouchine, A.-L., Kabri, Y., Bakhta, S., Curti, C., Nedjar-Kolli, B., & Vanelle, P. (2018). Simple synthesis of imidazo[1,2-A]pyridine derivatives bearing 2-aminonicotinonitrile or 2-aminochromene moiety. Synthetic Communications, 48(17), 2159–2168. https://doi.org/10.1080/00397911.2018.1479759
Barthod, L., Lopez, J.-G., Curti, C., Bornet, C., Roche, M., Montana, M., & Vanelle, P. (2018). News on therapeutic management of MDR-tuberculosis: a literature review. Journal of Chemotherapy, 30(1), 1–15. https://doi.org/10.1080/1120009X.2017.1338845
Mathias, F., Crozet, M. D., Kabri, Y., & Vanelle, P. (2018). Rapid synthesis of new 2-methyl-7-nitro-5-substituted-2,3-dihydroimidazo[5,1-b]oxazole as potential antibacterial drugs through one-pot cyclization and Suzuki-Miyaura coupling. Synthetic Communications, 48(10), 1213–1219. https://doi.org/10.1080/00397911.2018.1439177
Ibrahim-Ouali, M., & Dumur, F. (2018). Recent syntheses of ellipticine and its derivatives. Arkivoc, 216–243. https://doi.org/10.24820/ark.5550190.p010.445
Audran, G., Bagryanskaya, E., Edeleva, M., Marque, S. R. A., Parkhomenko, D., Tretyakov, E., & Zhivetyeva, S. (2018). Coordination-Initiated Nitroxide-Mediated Polymerization (CI-NMP). Australian Journal of Chemistry, 71(5), 334–340. https://doi.org/10.1071/CH17570
Moehl, G. E., Metwalli, E., Bouchet, R., Phan, T. N. T., Cubitt, R., & Mueller-Buschbaum, P. (2018). In Operando Small-Angle Neutron Scattering Study of Single-Ion Copolymer Electrolyte for Li-Metal Batteries. Acs Energy Letters, 3(1), 1–6. https://doi.org/10.1021/acsenergylett.7b01025
Bertrand, A., Dumur, F., Mruczkiewicz, M., Perrin, M., Lartigau-Dagron, C., Bousquet, A., Vignau, L., Billon, L., & Fasquel, S. (2018). Bottom-up honeycomb top layer for light outcoupling enhancement in blue organic light emitting diodes. Organic Electronics, 52, 222–229. https://doi.org/10.1016/j.orgel.2017.10.022
Dorey, S., Gaston, F., Marque, S. R. A., Bortolotti, B., & Dupuy, N. (2018). XPS analysis of PE and EVA samples irradiated at different gamma-doses. Applied Surface Science, 427, 966–972. https://doi.org/10.1016/j.apsusc.2017.09.001
Vibert, F., Bloch, E., Bertrand, M. P., Gastaldi, S., & Besson, E. (2018). Nanostructured Silicas, a Platform for the Observation of Transient Radicals: Application to Sulfinyl Radicals. Journal of Physical Chemistry C, 122(1), 681–686. https://doi.org/10.1021/acs.jpcc.7b10879
Karthikeyan, G., Bonucci, A., Casano, G., Gerbaud, G., Abel, S., Thome, V., Kodjabachian, L., Magalon, A., Guigliarelli, B., Belle, V., Ouari, O., & Mileo, E. (2018). A Bioresistant Nitroxide Spin Label for In-Cell EPR Spectroscopy: In Vitro and In Oocytes Protein Structural Dynamics Studies. Angewandte Chemie-International Edition, 57(5), 1366–1370. https://doi.org/10.1002/anie.201710184
Bui, T.-T., Goubard, F., Ibrahim-Ouali, M., Gigmes, D., & Dumur, F. (2018). Recent advances on organic blue thermally activated delayed fluorescence (TADF) emitters for organic light-emitting diodes (OLEDs). Beilstein Journal of Organic Chemistry, 14, 282–308. https://doi.org/10.3762/bjoc.14.18
Laville, F., Montana, M., Roux, N., Rathelot, P., Giorgi, R., & Vanelle, P. (2018). Factors limiting adherence to antiepileptic treatment: A French online patient survey. Journal of Clinical Pharmacy and Therapeutics, 43(1), 73–79. https://doi.org/10.1111/jcpt.12615
Verdoni, M., De Pomyers, H., Gigmes, D., Luis, J., Migan, N., Badirou, E. M., Amoussouga, S., Bengeloune, A. H., & Mabrouk, K. (2018). HPLC/SM method for the identification and the quantification of illicit substances possibly used as skin whitening agents in bleaching cosmetic products. Toxicologie Analytique Et Clinique, 30(1), 61–68. https://doi.org/10.1016/j.toxac.2017.09.001
Garra, P., Carre, M., Dumur, F., Morlet-Savary, F., Dietlin, C., Gigmes, D., Fouassier, J.-P., & Lalevee, J. (2018). Copper-Based (Photo)redox Initiating Systems Systems for Interpenetrating Polymer Network as Highly Efficient Preparation. Macromolecules, 51(3), 679–688. https://doi.org/10.1021/acs.macromol.7b02491
Naveen, P., Dallemer, F., Butcher, R. J., & Prabhakaran, R. (2018). New Ru(II) complexes containing tris(2-pyridylmethyl) amine. Synthesis, structural, CT-DNA/albumin interaction, anti-oxidant and cytotoxicity studies. Inorganica Chimica Acta, 471, 724–734. https://doi.org/10.1016/j.ica.2017.12.010
Bonardi, A. H., Dumur, F., Grant, T. M., Noirbent, G., Gigmes, D., Lessard, B. H., Fouassier, J.-P., & Lalevee, J. (2018). High Performance Near-Infrared (NIR) Photoinitiating Systems Operating under Low Light Intensity and in the Presence of Oxygen. Macromolecules, 51(4), 1314–1324. https://doi.org/10.1021/acs.macromol.8b00051
Zhang, J., Zivic, N., Dumur, F., Xiao, P., Graff, B., Fouassier, J. P., Gigmes, D., & Lalevee, J. (2018). N-[2-(Dimethylamino)ethyl]-1,8-naphthalimide derivatives as photoinitiators under LEDs. Polymer Chemistry, 9(8), 994–1003. https://doi.org/10.1039/c8py00055g
Baron, M., Morris, J. C., Telitel, S., Clement, J.-L., Lalevee, J., Morlet-Savary, F., Spangenberg, A., Malval, J.-P., Soppera, O., Gigmes, D., & Guillaneuf, Y. (2018). Light-Sensitive Alkoxyamines as Versatile Spatially- and Temporally-Controlled Precursors of Alkyl Radicals and Nitroxides. Journal of the American Chemical Society, 140(9), 3339–3344. https://doi.org/10.1021/jacs.7b12807
Arif, T., Borie, C., Jean, M., Vanthuyne, N., Bertrand, M. P., Siri, D., & Nechab, M. (2018). Organocopper triggered cyclization of conjugated dienynes via tandem S(N)2/Alder-ene reaction. Organic Chemistry Frontiers, 5(5), 769–776. https://doi.org/10.1039/c7qo00288b
Tintori, G., Nabokoff, P., Buhaibeh, R., Berge-Lefranc, D., Redon, S., Broggi, J., & Vanelle, P. (2018). Base-Free Generation of Organic Electron Donors from Air-Stable Precursors. Angewandte Chemie-International Edition, 57(12), 3148–3153. https://doi.org/10.1002/anie.201713079
Autissier, L., Mabrouk, K., Chendo, C., Guillaneuf, Y., Rollet, M., Charles, L., Gigmes, D., & Trimaille, T. (2018). Catalyst- and Initiator-Free Radical Addition under Mild Conditions: A Macromolecular Conjugation Tool. Chemistry-a European Journal, 24(15), 3699–3702. https://doi.org/10.1002/chem.201800035
Al Mousawi, A., Garra, P., Sallenave, X., Dumur, F., Toufaily, J., Hamieh, T., Graff, B., Gigmes, D., Fouassier, J. P., & Lalevee, J. (2018). pi-Conjugated Dithienophosphole Derivatives as High Performance Photoinitiators for 3D Printing Resins. Macromolecules, 51(5), 1811–1821. https://doi.org/10.1021/acs.macromol.8b00044
Chendo, C., Phan, T. N. T., Rollet, M., Gigmes, D., & Charles, L. (2018). Adduction of ammonium to polylactides to modify their dissociation behavior in collision-induced dissociation. Rapid Communications in Mass Spectrometry, 32(5), 423–430. https://doi.org/10.1002/rcm.8046
Tabele, C., Faioes, V. D. S., Grimaud, F., Torres-Santos, E. C., Khoumeri, O., Curti, C., & Vanelle, P. (2018). Original antileishmanial hits: Variations around amidoximes. European Journal of Medicinal Chemistry, 148, 154–164. https://doi.org/10.1016/j.ejmech.2018.02.029
Borie, C., Mondal, S., Arif, T., Briand, M., Lingua, H., Dumur, F., Gigmes, D., Stocker, P., Barbarat, B., Robert, V., Nicoletti, C., Olive, D., Maresca, M., & Nechab, M. (2018). Enediynes bearing polyfluoroaryl sulfoxide as new antiproliferative agents with dual targeting of microtubules and DNA. European Journal of Medicinal Chemistry, 148, 306–313. https://doi.org/10.1016/j.ejmech.2018.02.030
Garra, P., Morlet-Savary, F., Graff, B., Dumur, F., Monnier, V., Dietlin, C., Gigmes, D., Fouassier, J. P., & Lalevee, J. (2018). Metal Acetylacetonate-Bidentate Ligand Interaction (MABLI) as highly efficient free radical generating systems for polymer synthesis. Polymer Chemistry, 9(12), 1371–1378. https://doi.org/10.1039/c8py00238j
Ouedrago, M., Abou, A., Djande, A., Ouari, O., & Zoueu, T. J. (2018). 2-Oxo-2H-chromen-7-yl 4-tert-butylbenzoate. Acta Crystallographica Section E-Crystallographic Communications, 74, 530-+. https://doi.org/10.1107/S2056989018004188
Ouari, O., & Bardelang, D. (2018). Nitroxide Radicals with Cucurbit[n]urils and Other Cavitands. Israel Journal of Chemistry, 58(3–4), 343–356. https://doi.org/10.1002/ijch.201700115
Kalyanaraman, B., Cheng, G., Hardy, M., Ouari, O., Lopez, M., Joseph, J., Zielonka, J., & Dwinell, M. B. (2018). A review of the basics of mitochondrial bioenergetics, metabolism, and related signaling pathways in cancer cells: Therapeutic targeting of tumor mitochondria with lipophilic cationic compounds. Redox Biology, 14, 316–327. https://doi.org/10.1016/j.redox.2017.09.020
Garcia-Iriepa, C., Gosset, P., Berraud-Pache, R., Zemmouche, M., Taupier, G., Dorkenoo, K. D., Didier, P., Leonard, J., Ferre, N., & Navizet, I. (2018). Simulation and Analysis of the Spectroscopic Properties of Oxyluciferin and Its Analogues in Water. Journal of Chemical Theory and Computation, 14(4), 2117–2126. https://doi.org/10.1021/acs.jctc.7b01240
Rossi, F., Cerreia Vioglio, P., Bordignon, S., Giorgio, V., Nervi, C., Priola, E., Gobetto, R., Yazawa, K., & Chierotti, M. R. (2018). Unraveling the Hydrogen Bond Network in a Theophylline-Pyridoxine Salt Cocrystal by a Combined X-ray Diffraction, Solid State NMR, and Computational Approach. Crystal Growth & Design, 18(4), 2225–2233. https://doi.org/10.1021/acs.cgd.7b01662
Dumur, F., Ibrahim-Ouali, M., & Gigmes, D. (2018). Organic Light-Emitting Diodes Based on Phthalimide Derivatives: Improvement of the Electroluminescence Properties. Applied Sciences-Basel, 8(4), 539. https://doi.org/10.3390/app8040539
Bui, T.-T., Goubard, F., Ibrahim-Ouali, M., Gigmes, D., & Dumur, F. (2018). Thermally Activated Delayed Fluorescence Emitters for Deep Blue Organic Light Emitting Diodes: A Review of Recent Advances. Applied Sciences-Basel, 8(4), 494. https://doi.org/10.3390/app8040494
Agathangelou, D., Orozco-Gonzalez, Y., del Carmen Marin, M., Roy, P. P., Brazard, J., Kandori, H., Jung, K.-H., Leonard, J., Buckup, T., Ferre, N., Olivucci, M., & Haacke, S. (2018). Effect of point mutations on the ultrafast photo-isomerization of Anabaena sensory rhodopsin. Faraday Discussions, 207, 55–75. https://doi.org/10.1039/c7fd00200a
Garra, P., Dumur, F., Gigmes, D., Nechab, M., Morlet-Savary, F., Dietlin, C., Gree, S., Fouassier, J. P., & Lalevee, J. (2018). Metal Acetylacetonate-Bidentate Ligand Interaction (MABLI) (Photo)activated Polymerization: Toward High Performance Amine-Free, Peroxide-Free Redox Radical (Photo)initiating Systems. Macromolecules, 51(7), 2706–2715. https://doi.org/10.1021/acs.macromol.8b00163
Devaux, D., Lienafa, L., Beaudoin, E., Maria, S., Phan, T. N. T., Gigmes, D., Giroud, E., Davidson, P., & Bouchet, R. (2018). Comparison of single-ion-conductor block-copolymer electrolytes with Polystyrene-TFSI and Polymethacrylate-TFSI structural blocks. Electrochimica Acta, 269, 250–261. https://doi.org/10.1016/j.electacta.2018.02.142
Yin, H., Huang, Q., Zhao, W., Bardelang, D., Siri, D., Chen, X., Lee, S. M. Y., & Wang, R. (2018). Supramolecular Encapsulation and Bioactivity Modulation of a Halonium Ion by Cucurbit[n]uril (n=7, 8). Journal of Organic Chemistry, 83(8), 4882–4887. https://doi.org/10.1021/acs.joc.8b00543
Garra, P., Dumur, F., Nechab, M., Morlet-Savary, F., Dietlin, C., Graff, B., Gigmes, D., Fouassier, J.-P., & Lalevee, J. (2018). Stable copper acetylacetonate-based oxidizing agents in redox (NIR photoactivated) polymerization: an opportunity for the one pot grafting from approach and an example on a 3D printed object. Polymer Chemistry, 9(16), 2173–2182. https://doi.org/10.1039/c8py00341f
Curti, C., Gallice, S., Lamy, E., Rathelot, P., & Vanelle, P. (2018). [City-hospital network and quality control of officinal preparations]. Annales Pharmaceutiques Francaises, 76(3), 242–247. https://doi.org/10.1016/j.pharma.2017.09.003
Audran, G., Bagryanskaya, E. G., Bagryanskaya, I. Y., Edeleva, M., Kaletina, P., Marque, S. R. A., Parkhomenko, D., Tretyakov, E. V., & Zhivetyeva, S. I. (2018). The effect of the oxophilic Tb(III) cation on C-ON bond homolysis in alkoxyamines. Inorganic Chemistry Communications, 91, 5–7. https://doi.org/10.1016/j.inoche.2018.02.019
Kalyanaraman, B., Cheng, G., Hardy, M., Ouari, O., Bennett, B., & Zielonka, J. (2018). Teaching the basics of reactive oxygen species and their relevance to cancer biology: Mitochondrial reactive oxygen species detection, redox signaling, and targeted therapies. Redox Biology, 15, 347–362. https://doi.org/10.1016/j.redox.2017.12.012
Savelli, M., Roche, M., Curti, C., Bornet, C., Rathelot, P., Montana, M., & Vanelle, P. (2018). Methods to control anticancer chemotherapy preparations ranked by risk analysis. Pharmazie, 73(5), 251–259. https://doi.org/10.1691/ph.2018.7205
Gaston, F., Dupuy, N., Marque, S. R. A., & Dorey, S. (2018). Evaluation of multilayer film stability by Raman spectroscopy after gamma-irradiation sterilization process. Vibrational Spectroscopy, 96, 52–59. https://doi.org/10.1016/j.vibspec.2018.03.002
Pierrisnard, C., Baciuchka, M., Mancini, J., Rathelot, P., Vanelle, P., & Montana, M. (2018). Body image and psychological distress in women with breast cancer: a French online survey on patients’ perceptions and expectations. Breast Cancer, 25(3), 303–308. https://doi.org/10.1007/s12282-017-0828-2
Al Mousawi, A., Arar, A., Ibrahim-Ouali, M., Duval, S., Dumur, F., Garra, P., Toufaily, J., Hamieh, T., Graff, B., Gigmes, D., Fouassier, J.-P., & Lalevee, J. (2018). Carbazole-based compounds as photoinitiators for free radical and cationic polymerization upon near visible light illumination. Photochemical & Photobiological Sciences, 17(5), 578–585. https://doi.org/10.1039/c7pp00400a