Molenberg, I., Huynen, I., Baudouin, A.-C., Bailly, C., Thomassin, J.-M., & Detrembleur, C. (2010). Foamed nanocomposites for EMI shielding applications. In M. Mukherjee (Ed.), Advanced Microwave and Milimeter Wave Technologies Semiconductor Devices Circuits and Systems (pp. 453-470). InTech. |
Pierrard, A., Ferreira Melo, S., Thijssen, Q., Van Vlierberghe, S., Lancellotti, P., Oury, C., Detrembleur, C., & Jérôme, C. (In press). Design of 3D-Photoprintable, Bio-, and Hemocompatible Nonisocyanate Polyurethane Elastomers for Biomedical Implants. Biomacromolecules. doi:10.1021/acs.biomac.3c01261 |
Delcorps, J., Rawat, K. S., Wells, M., Ben Ayed, E., Grignard, B., Detrembleur, C., Blankert, B., Gerbaux, P., Van Speybroeck, V., & Coulembier, O. (2024). Turning carbon dioxide into dialkyl carbonates through guanidinium-assisted SN2 ion-pair process. Cell Reports. Physical Science, 102057. doi:10.1016/j.xcrp.2024.102057 |
Muzyka, C., Renson, S., Grignard, B., Detrembleur, C., & Monbaliu, J.-C. (2024). Intensified Continuous Flow Process for the Scalable Production of Bio-Based Glycerol Carbonate. Angewandte Chemie International Edition, 202319060. doi:10.1002/anie.202319060 |
Habets, T., Seychal, G., Caliari, M., Raquez, J.-M., Sardon, H., Grignard, B., & Detrembleur, C. (22 November 2023). Covalent Adaptable Networks through Dynamic N,S-Acetal Chemistry: Toward Recyclable CO2-Based Thermosets. Journal of the American Chemical Society, 145 (46), 25450 - 25462. doi:10.1021/jacs.3c10080 |
Pierrard, A., Aqil, A., Detrembleur, C., & Jérôme, C. (09 October 2023). Thermal and UV curable formulations of poly(propylene glycol)−poly(hydroxyurethane) elastomers toward nozzle-based 3D photoprinting. Biomacromolecules, 24 (10), 4375–4384. doi:10.1021/acs.biomac.2c00860 Dataset: 10.1021/acs.biomac.2c00860 |
Habets, T., Olmedo-Martínez, J. L., Del Olmo, R., Grignard, B., Mecerreyes, D., & Detrembleur, C. (21 July 2023). Facile access to CO2-sourced polythiocarbonate dynamic networks and their potential as solid-state electrolytes for lithium metal batteries. ChemSusChem, 16 (14), 202300225. doi:10.1002/cssc.202300225 |
Seychal, G., Ocando, C., Bonnaud, L., De Winter, J., Grignard, B., Detrembleur, C., Sardon, H., Aramburu, N., & Raquez, J.-M. (14 July 2023). Emerging polyhydroxyurethanes as sustainable thermosets: a structure–property relationship. ACS Applied Polymer Materials, 5 (7), 5567 - 5581. doi:10.1021/acsapm.3c00879 |
Bryaskova, R., Philipova, N., Georgiev, N., Ganchev, D., Lalov, I., & Detrembleur, C. (11 June 2023). Bio-inspired antibacterial polymer coatings with included silver nanoparticles and porphyrin-based photosensitizer. Journal of Polymer Research, 30 (6), 1999. doi:10.1007/s10965-023-03572-2 |
Lancellotti, P., Aqil, A., MUSUMECI, L., Jacques, N., Ditkowski, B., Debuisson, M., Thiry, M., Dupont, J., Gougnard, A., Sandersen, C., CHERAMY-BIEN, J.-P., Sakalihasan, N., Nchimi Longang, A., Detrembleur, C., Jérôme, C., & Oury, C. (2023). Bioactive surface coating for preventing mechanical heart valve thrombosis. Journal of Thrombosis and Haemostasis. doi:10.1016/j.jtha.2023.05.004 |
Siragusa, F., Detrembleur, C., & Grignard, B. (21 March 2023). The advent of recyclable CO2-based polycarbonates. Polymer Chemistry, 10 (27), 8863-8875. doi:10.1039/d2py01258h |
Lecart, B., Baumsteiger, C., Monie, F., Di Maria, A., Detrembleur, C., Richel, A., & Vanderschuren, H. (2023). Towards green chemicals and edible coatings from barks and peels with near critical extraction of suberin. Green Chemistry. doi:10.1039/d3gc02552g |
Bourguignon, M., Grignard, B., & Detrembleur, C. (19 December 2022). Water‐induced self‐blown non‐isocyanate polyurethane foams. Angewandte Chemie International Edition, 61 (51), 202213422. doi:10.1002/anie.202213422 Dataset: 10.1002/anie.202213422 |
Grignard, B., Mampuys, P., Escudero, J., Masullo, D., Lemière, F., Maes, B. U. W., & Detrembleur, C. (08 November 2022). Functional regioregular (poly)urethanes from soft nucleophiles and cyclic iminocarbonates. Polymer Chemistry, 13 (48), 6599 - 6605. doi:10.1039/d2py01077a |
Habets, T., Siragusa, F., Müller, A. J., Grossman, Q., Ruffoni, D., Grignard, B., & Detrembleur, C. (07 June 2022). Facile construction of functional poly(monothiocarbonate) copolymers under mild operating conditions. Polymer Chemistry, 13 (21), 3076-3090. doi:10.1039/d2py00307d |
Li, X., Villar-Yanez, A., Ngassam Tounzoua, C., Benet-Buchholz, J., Grignard, B., Bo, C., Detrembleur, C., & Kleij, A. W. (15 February 2022). Cascade transformation of carbon dioxide and alkyne-1,n-diols into densely substituted cyclic carbonates. ACS Catalysis, 12 (5), 2854-2860. doi:10.1021/acscatal.1c05773 |
Monie, F.* , Grignard, B.* , & Detrembleur, C.*. (15 February 2022). Divergent aminolysis approach for constructing recyclable self-blown nonisocyanate polyurethane foams. ACS Macro Letters, 11 (2), 236-242. doi:10.1021/acsmacrolett.1c00793 * These authors have contributed equally to this work. |
Brege, A., Grignard, B., Méreau, R., Detrembleur, C., Jérôme, C., & Tassaing, T. (20 January 2022). En route to CO2-based (a)cyclic carbonates and polycarbonates from alcohols substrates by direct and indirect approaches. Catalysts, 12 (2), 124. doi:10.3390/catal12020124 |
Gomez-Lopez, A., Ayensa, N., Grignard, B., Irusta, L., Iñigo, C., Müller, A. J., Detrembleur, C., & Sardon, H. (10 January 2022). Enhanced and reusable poly(hydroxy urethane)-based low temperature hot-melt adhesives. ACS Applied Polymer Materials, 2 (3), 194.207. doi:10.1021/acspolymersau.1c00053 |
Habets, T., Siragusa, F., Grignard, B., & Detrembleur, C. (11 August 2020). Advancing the synthesis of isocyanate-free poly(oxazolidones)s: scope and limitations. Macromolecules, 53 (15), 6393-6408. doi:10.1021/acs.macromol.0c01231 |
Moreno-Couranjou, M., Guillot, J., Audinot, J.-N., Bour, J., Prouvé, E., Durrieu, M.-C., Choquet, P., & Detrembleur, C. (July 2020). Atmospheric pulsed plasma copolymerization of acrylic monomers: Kinetics, chemistry, and applications. Plasma Processes and Polymers, 17 (7). doi:10.1002/ppap.201900187 |
Jalaber, V., Del Frari, D., De Winter, J., Mehennaoui, K., Planchon, S., Choquet, P., Detrembleur, C., & Moreno-Couranjou, M. (02 April 2019). Atmospheric aerosol assisted pulsed plasma polymerization: An environmentally friendly technique for tunable catechol-bearing thin films. Frontiers in Chemistry, 7, 183. doi:10.3389/fchem.2019.00183 |
Scholten, P., Demarteau, J., Gennen, S., De Winter, J., Grignard, B., Debuigne, A., Meier, M. A. R., & Detrembleur, C. (08 May 2018). Merging CO2‑based building blocks with cobalt-mediated radical polymerization for the synthesis of functional poly(vinyl alcohol)s. Macromolecules, 51 (9), 3379-3393. doi:10.1021/acs.macromol.8b00492 |
Banerjee, S., Bellan, E. V., Gayet, F., Debuigne, A., Detrembleur, C., Poli, R., Améduri, B., & Ladmiral, V. (December 2017). Bis(formylphenolato)cobalt(II)-mediated alternating radical copolymerization of tert-butyl 2-trifluoromethylacrylate with vinyl acetate. Polymers, 9 (12), 705. doi:10.3390/polym9120702 |
Defteralı, Ç., Verdejo, R., Majeed, S., Boschetti-de-Fierro, A., Méndez-Gómez, H. R., Díaz-Guerra, E., Fierro, D., Buhr, K., Abetz, C., Martínez-Murillo, R., Vuluga, D., Alexandre, M., Thomassin, J.-M., Detrembleur, C., Jérôme, C., Abetz, V., López-Manchado, M. Á., & Vicario-Abejón, C. (06 December 2016). In vitro evaluation of biocompatibility of uncoated thermally reduced graphene and carbon nanotube-loaded PVDF membranes with adult neural stem cell-derived neurons and glia. Frontiers in Bioengineering and Biotechnology, 4 (n° 64). doi:10.3389/fbioe.2016.00094 |
Wan, F., Tran, M. P., Leblanc, C., Béchet, E., Plougonven, E., Léonard, A., Detrembleur, C., Noels, L., Thomassin, J.-M., & Nguyen, V. D. (December 2015). Experimental and computational micro–mechanical investigations of compressive properties of polypropylene/multi–walled carbon nanotubes nanocomposite foams. Mechanics of Materials, 91 (Part 1), 95-118. doi:10.1016/j.mechmat.2015.07.004 |
Alves, M., Grignard, B., Gennen, S., Detrembleur, C., Jérôme, C., & Tassaing, T. (2015). Organocatalytic synthesis of bio-based cyclic carbonates from CO2 and vegetable oils. RSC Advances, 5, 53629-53636. doi:10.1039/C5RA10190E |
Kermagoret, A., Jérôme, C., Detrembleur, C., & Debuigne, A. (January 2015). In situ bidentate to tetradentate ligand exchange reaction in cobalt-mediated radical polymerization. European Polymer Journal, 62, 312-321. doi:10.1016/j.eurpolymj.2014.08.003 |
Faure, E., Falentin-Daudré, C., Jérôme, C., Lyskawa, J., Fournier, D., Woisel, P., & Detrembleur, C. (January 2013). Catechols as versatile platforms in polymer chemistry. Progress in Polymer Science, 38 (1), 236-270. doi:10.1016/j.progpolymsci.2012.06.004 |
Faure, E., Lecomte, P., Lenoir, S., Vreuls, C., Van de Weerdt, C., Archambeau, C., Martial, J., Jérôme, C., Duwez, A.-S., & Detrembleur, C. (03 May 2011). Sustainable and bio-inspired chemistry for robust antibacterial activity of stainless steel. Journal of Materials Chemistry, 21 (22), 7901-7904. doi:10.1039/c1jm11380a |
Brzozowska, A. M., de Keizer, A., Detrembleur, C., Cohen Stuart, M. A., & Norde, W. (November 2010). Grafted ionomer complexes and their effect on protein adsorption on silica and polysulfone surfaces. Colloid and Polymer Science, 288 (16/17), 1621-1632. doi:10.1007/s00396-010-2295-6 |
Brzozowska, A. M., de Keizer, A., Norde, W., Detrembleur, C., & Cohen Stuart, M. A. (July 2010). Grafted block complex coacervate core micelles and their effect on protein adsorption on silica and polystyrene. Colloid and Polymer Science, 288 (10/11), 1081-1095. doi:10.1007/s00396-010-2228-4 |
Urbanczyk, L., Bourbigot, S., Calberg, C., Detrembleur, C., Jérôme, C., Boschini, F., & Alexandre, M. (05 January 2010). Preparation of fire-resistant poly(styrene-co-acrylonitrile) foams using supercritical CO2 technology. Journal of Materials Chemistry, 20, 1567-1576. doi:10.1039/b917539c |
Grignard, B., Schmeits, S., Riva, R., Detrembleur, C., Lecomte, P., & Jérôme, C. (November 2009). First example of “click” copper(I) catalyzed azide-alkyne cycloaddition in supercritical carbon dioxide: Application to the functionalization of aliphatic polyesters. Green Chemistry, 11, 1525-1529. doi:10.1039/b822924d |
Voets, I. K., de Keizer, A., Leermakers, F. A. M., Debuigne, A., Jérôme, R., Detrembleur, C., & Cohen Stuart, M. A. (October 2009). Electrostatic hierarchical co-assembly in aqueous solutions of two oppositevely charged double hydrophilic diblock copolymers. European Polymer Journal, 45 (10), 2913-2925. doi:10.1016/j.eurpolymj.2009.06.020 |
Debuigne, A., Poli, R., Jérôme, C., Jérôme, R., & Detrembleur, C. (March 2009). Overview of cobalt-mediated radical polymerization: roots, state of the art and future prospects. Progress in Polymer Science, 34 (3), 211-239. doi:10.1016/j.progpolymsci.2008.11.003 |
Naveau, E., Detrembleur, C., Jérôme, C., & Alexandre, M. (January 2009). Patenting activity in manufacturing organoclays for nanocomposite applications. Recent Patents on Materials Science, 2 (1), 43-49. doi:10.2174/1874464810902010043 |
Urbanczyk, L., Calberg, C., Benali, S., Bourgibot, S., Espuche, E., Gouanvé, F., Dubois, P., Germain, A., Jérôme, C., Detrembleur, C., & Alexandre, M. (August 2008). Poly(caprolactone)/clay masterbatches prepared in supercritical CO2 as efficient clay delamination promoters in poly(styrene-co-acrylonitrile). Journal of Materials Chemistry, 18 (39), 4623-4630. doi:10.1039/b807357k |
Grignard, B., Jérôme, C., Calberg, C., Jérôme, R., & Detrembleur, C. (March 2008). Atom transfer radical polymerization of MMA with a macromolecular ligand in a fluorinated solvent and in supercritical carbon dioxide. European Polymer Journal, 44 (3), 861-871. doi:10.1016/j.eurpolymj.2007.11.020 |
Grignard, B., Calberg, C., Jérôme, C., Wang, W., Howdle, S., & Detrembleur, C. (2008). Supported ATRP of fluorinated methacrylates in supercritical carbon dioxide : preparation of scCO2 soluble polymers with low catalytic residues. Chemical Communications, (44), 5803-5805. doi:10.1039/b812297k |
Charlot, A., Gabriel, S., Detrembleur, C., Jérôme, R., & Jérôme, C. (2007). Combination of electrografting and layer-by-layer deposition: an efficient way to tailor polymer coatings of (semi)-conductors. Chemical Communications, (44), 4656-4658. doi:10.1039/b712130j |
Thomassin, J.-M., Kollar, J., Caldarella, G., Germain, A., Jérôme, R., & Detrembleur, C. (15 October 2007). Beneficial effect of carbon nanotubes on the performances of Nafion membranes in fuel cell applications. Journal of Membrane Science, 303 (1-2), 252-257. doi:10.1016/j.memsci.2007.07.019 |
Hajek, J., Dams, M., Detrembleur, C., Jérôme, R., Jacobs, P. A., & De Vos, D. E. (July 2007). Heterogeneous alkenylation of aromatics under oxygen. Catalysis Communications, 8 (7), 1047-1051. doi:10.1016/j.catcom.2006.10.020 |
Stoilova, O., Jérôme, C., Detrembleur, C., Mouithys-Mickalad, A., Manolova, N., Rashkov, I., & Jérôme, R. (23 March 2007). C-60-containing nanostructured polymeric materials with potential biomedical applications. Polymer, 48 (7), 1835-1843. doi:10.1016/j.polymer.2007.02.026 |
Sciannamea, V., Debuigne, A., Piette, Y., Jérôme, R., & Detrembleur, C. (2006). Supported cobalt mediated radical polymerization (SCMRP) of vinyl acetate and recycling of the cobalt complex. Chemical Communications, (40), 4180-4182. doi:10.1039/b610455j |
Lenoir, S., Pagnoulle, C., Detrembleur, C., Galleni, M., & Jérôme, R. (26 October 2005). Antimicrobial activity of polyestyrene particles coated by photo-crooslinked block copolymers containing a biocidal polymethacrylate block. e-Polymers, 74, 1-11. |
Stoffelbach, F., Aqil, A., Jérôme, C., Jérôme, R., & Detrembleur, C. (2005). An easy and economically viable route for the decoration of carbon nanotubes by magnetite nanoparticles, and their orientation in a magnetic field. Chemical Communications, (36), 4532-4533. doi:10.1039/b506758h |
Lou, X., Detrembleur, C., Sciannamea, V., Pagnoulle, C., & Jérôme, R. (19 August 2004). Grafting of alkoxyamine end-capped (co)polymers onto multi-walled carbon nanotubes. Polymer, 45 (18), 6097-6102. doi:10.1016/j.polymer.2004.06.050 |
Lou, X., Detrembleur, C., Lecomte, P., & Jérôme, R. (2002). Novel unsaturated epsilon-caprolactone polymerizable by ring-opening and ring-opening metathesis mechanisms. e-Polymers, (34), 1-12. |
Detrembleur, C., Mouithys-Mickalad, A., Teyssié, P., & Jérôme, R. (2002). Sodium nitrite and ascorbic acid: a metal-free combination that controls the free-radical polymerization of tert-butyl methacrylate in water. e-Polymers, (4), 1-16. doi:10.1515/epoly.2002.2.1.53 |
Detrembleur, C., Jérôme, C., Claes, M., Louette, P., & Jérôme, R. (01 April 2001). Combination of Electrografting and Ring-Opening Metathesis Polymerization: An Efficient Way to Prepare Polynorbornene Brushes on Conducting Substrates. Angewandte Chemie International Edition, 40 (7), 1268-1271. doi:10.1002/1521-3773(20010401)40:7<1268::AID-ANIE1268>3.0.CO;2-A |
Plougonven, E., Marchot, P., Detrembleur, C., Tran, M. P., & Léonard, A. (2011). Methodology for the characterization of the microstructure of nanocomposite polymeric foams using X-ray microtomography. In Micro-CT User Meeting Abstract Book. |
Detrembleur, C., Grignard, B., & Monie, F. (December 2023). Self-blowing isocyanate-free polyurethane foams. |
Detrembleur, C., Grignard, B., & Bourguignon, M. (15 June 2023). Self-blowing isocyanate-free polyurethane foams. |
Pierrard, A., Aqil, A., Detrembleur, C., Jérôme, C., LANCELLOTTI, P., Oury, C., & Ferreira Melo, S. (01 September 2022). New antimicrobial and antithrombogenic medical device. |
Takayama, T., Maekawa, K., Detrembleur, C., Debuigne, A., & Jérôme, C. (20 May 2020). Polyvinyl alcohol and method for producing polyvinyl alcohol. |
Detrembleur, C., Demarteau, J., Debuigne, A., & Kermagoret, A. (27 June 2019). Block copolymerization of ethylene by cobalt-mediated radical polymerization. |
Takayama, T., Amano, Y., Maekawa, K., Detrembleur, C., Debuigne, A., & Jérôme, C. (05 October 2017). Polyvinyl alcohol and method for producing same. |
Detrembleur, C., Van de Weerdt, C., Vreuls, C., Mauchauffe, R., Moreno-Couranjou, M., Boscher, N., & Choquet, P. (07 April 2016). Plasma deposition method for catechol/quinone functionalised layers. |
Herwats, S., Detrembleur, C., Alexandre, M., & Jérôme, C. (26 June 2013). Composition and preparation of hydrogel nanocomposites with improved mechanical properties and use thereof. |
Bodart, V., Piette, Y., Detrembleur, C., Debuigne, A., & Jérôme, C. (14 June 2012). Controlled radical polymerization of halogenated monomers. |
Bodart, V., Piette, Y., Detrembleur, C., Debuigne, A., & Jérôme, C. (14 June 2012). Controlled radical polymerization of halogenated monomers. |
Detrembleur, C., Huynen, I., Thomassin, J.-M., Furnemont, Q., Pardoen, T., Bailly, C., Eggermont, S., Quievy, N., Urbanczyk, L., & Molenberg, I. (15 March 2012). Hybrid material for electromagnetic absorption. |
Detrembleur, C., Molenberg, I., Huynen, I., Thomassin, J.-M., Furnemont, Q., Pardoen, T., Bailly, C., Eggermont, S., Quievy, N., & Urbanczyk, L. (15 March 2012). Hybrid material for electromagnetic absorption. |
Thomassin, J.-M., Jérôme, C., Detrembleur, C., Alexandre, M., & Huynen, I. (08 March 2012). Process for preparing electromagnetic interference shileding materials. |
Thomassin, J.-M., Jérôme, C., Detrembleur, C., Alexandre, M., & Huynen, I. (07 March 2012). Process for preparing electromagnetic interference shileding materials. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (14 June 2011). Low-viscosity allophanates containing actinically curable groups. |
Weikard, J., Detrembleur, C., Greszta-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (26 May 2011). Low viscosity allophanates containing actinically curable groups. |
Van de Weerdt, C., Detrembleur, C., Charlot, A., Jérôme, R., Vreuls, C., & Zocchi, G. (31 March 2011). Multifunctional coatings. |
Weikard, J., Detrembleur, C., Greszta-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (08 March 2011). Low viscosity allophanates containing actinically curable groups. |
Van de Weerdt, C., Detrembleur, C., Charlot, A., Jérôme, R., Vreuls, C., & Zocchi, G. (02 March 2011). Multifunctional coatings. |
Greszta-Frank, D., Detrembleur, C., Weikard, J., Richter, F., Fischer, W., Mundstock, H., & Schmitz, J. (26 January 2011). Niedrigviskose allophanate mit aktinisch härtbaren gruppen. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (15 September 2010). Low viscosity allophanates containing actinically hardenable groups. |
Jérôme, R., Pagnoulle, C., Detrembleur, C., Thomassin, J.-M., Huynen, I., Bailly, C., Bednarz, L., Daussin, R., Saib, A., Baudouin, A.-C., & Laloyaux, X. (01 April 2010). Polymer composite material structures comprising carbon based conductive loads. |
Schmitz, J., Detrembleur, C., Fischer, W., Weikard, J., Greszta-Franz, D., & Mundstock, H. (04 February 2010). Production of novel radiation-hardening binding agents. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Fischer, W., Schmitz, J., & Mundstock, H. (22 December 2009). Herstellung von neuen strahlenhärtenden bindemitteln. |
Van de Weerdt, C., Detrembleur, C., Jérôme, R., & Charlot, A. (09 December 2009). Multifunctional coatings. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Fischer, W., Schmitz, J., & Mundstock, H. (16 September 2009). Herstellung von neuen strahlenhärtenden bindemitteln. |
Jérôme, R., Pagnoulle, C., Detrembleur, C., Thomassin, J.-M., Huynen, I., Bailly, C., Bednarz, L., Daussin, R., Saib, A., Baudouin, A.-C., & Laloyaux, X. (19 August 2009). Polymer composite material structures comprising carbon based conductive loads. |
Detrembleur, C., Weikard, J., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (22 July 2009). Low-viscosity allophanates having actinically hardenable groups. |
Detrembleur, C., Weikard, J., Fischer, W., Schmitz, J., & Mundstock, H. (08 July 2009). Production of novel radiation-hardening binding agent. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (04 September 2008). Low-viscosity allophanates containing actinically curable groups. |
Jérôme, R., Pagnoulle, C., Detrembleur, C., Thomassin, J.-M., Huynen, I., Bailly, C., Bednarz, L., Daussin, R., Saib, A., Baudouin, A.-C., & Laloyaux, X. (12 June 2008). Polymer composite material structures comprising carbon based conductive loads. |
Jérôme, R., Pagnoulle, C., Detrembleur, C., Thomassin, J.-M., Huynen, I., Bailly, C., Bednarz, L., Daussin, R., & Saib, A. (11 June 2008). Polymer composite material structures comprising carbon based conductive loads. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Fischer, W., Schmitz, J., & Mundstock, H. (03 June 2008). Preparation of new radiation-curing binders. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (22 April 2008). Low viscosity allophanates containing actinically curable groups. |
Detrembleur, C., Weikard, J., Greszta-Frank, D., Fischer, W., Schmitz, J., & Mundstock, H. (14 August 2007). Herstellung von neuen strahlenhärtenden Bindemitteln. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (07 August 2007). Niedrigviskose allophanate mit aktinisch härtbaren gruppen. |
Detrembleur, C. (21 March 2007). Production of novel radiation-hardening binding agents. |
Detrembleur, C. (21 March 2007). Low-viscosity allophanates having actinically hardenable groups. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (17 January 2007). Low viscosity allophanates containing actinically hardenable groups. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Fischer, W., Scmitz, J., & Mundstock, H. (06 December 2006). Production of novel radiation-hardening binding agents. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Fischer, W., Schmitz, J., & Mundstock, H. (05 December 2006). Production of novel radiation-hardening binding agents. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (05 December 2006). Low viscosity allophanates containing actinically hardenable groups. |
Detrembleur, C., Rüdiger, C., & Meyer, R.-V. (01 November 2006). The in situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary amines. |
Detrembleur, C. (24 April 2006). Radiation-curing binders and a process for their preparation. |
Weikard, J., Detrembleur, C., Greszta-Frank, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (13 April 2006). Low viscosity allophanates containing actinically curable groups. |
Weikard, J., Greszta-Franz, D., Fischer, W., Schmitz, J., Mundstock, H., & Detrembleur, C. (13 April 2006). Radiation-curing binders and a process for their preparation. |
Detrembleur, C., Rüdiger, C., & Meyer, R.-V. (22 March 2006). The in situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary amines. |
Weikard, J., Detrembleur, C., Greszta-Franz, D., Fischer, W., Schmitz, J., & Mundstock, H. (16 March 2006). Radiation-curing binders and a process for their preparation. |
Weikard, J., & Detrembleur, C. (15 March 2006). Radiation-curing binders and a process for their preparation. |
Weikard, J., Detrembleur, C., Grestza-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (15 March 2006). Low-viscosity allophanates having actinically hardenable groups. |
Weikard, J., Greszta-Franz, D., Fischer, W., Schmitz, J., Mundstock, H., & Detrembleur, C. (15 March 2006). Herstellung von neuen strahlenhärtbarenden Bindemitteln. |
Detrembleur, C., Mundstock, H., Greszta-Franz, D., Richter, F., Schmitz, J., Weikard, J., & Fischer, W. (09 March 2006). Low viscosity allophanates containing actinically curable groups. |
Greszta-Franz, D., Fischer, W., Weikard, J., Detrembleur, C., Mundstock, H., & Schmitz, J. (09 March 2006). Radiation-curing binders and a process for their preparation. |
Weikard, J., Detrembleur, C., Grestza-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (09 March 2006). Low viscosity allophanates containing actinically curable groups. |
Weikard, J., Greszta-Franz, D., Fischer, W., Schmitz, J., Mundstock, H., & Detrembleur, C. (09 March 2006). Radiation-curing binders and a process for their preparation. |
Detrembleur, C., Weikard, J., Geszta-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (06 October 2005). Low viscosity allophanates having actinically hardenable groups. |
Detrembleur, C., Weikard, J., Grestza-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (06 October 2005). Niedrigviskose Allophanate mit aktinisch härtbaren Gruppen. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Fischer, W., Schmitz, J., & Mundstock, H. (06 October 2005). Production of novel radiation-hardening binding agents. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Fischer, W., Schmitz, J., & Mundstock, H. (06 October 2005). Herstellung von neuen strahlenhärtenden bindemitteln. |
Mundstock, H., Schmitz, J., Detrembleur, C., Weikard, J., Fischer, W., & Grestza-Franz, D. (06 October 2005). Production of novel radiation-hardening binding agents. |
Schmitz, J., Detrembleur, C., Fischer, W., Weikard, J., Greszta-Franz, D., & Mundstock, H. (06 October 2005). Production of novel radiation-hardening binding agents. |
Schmitz, J., Mundstock, H., Fischer, W., Weikard, J., Detrembleur, C., Greszta-Franz, D., & Richter, F. (06 October 2005). Low viscosity allophanates having actinically hardenable groups. |
Detrembleur, C., Weikard, J., Grestza-Franz, D., Richter, F., Fischer, W., Schmitz, J., & Mundstock, H. (22 September 2005). Low viscosity allophanates containing actinically curable groups. |
Detrembleur, C., Weikard, J., Greszta-Franz, D., Fischer, W., Schmitz, J., & Mundstock, H. (22 September 2005). Preparation of new radiation-curing binders. |
Bertrand, O., Jérôme, R., Gautier, S., Maquet, V., Detrembleur, C., Jérôme, C., Voccia, S., Claes, M., Lou, X., & Labaye, D.-E. (29 July 2004). Process for depositing strong adherend polymer coating onto an electrically conductive surface. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (15 July 2004). In-situ polymerization of monoethylenically unsaturated monomers with secondary amines. |
Detrembleur, C., Rüdiger, C., & Meyer, R.-V. (15 July 2004). In-situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary amines. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (26 June 2004). Polymerization method of polymer compound by in situ polymerization of monoethylenically unsaturated monomer and secondary amine. |
Detrembleur, C., Rüdiger, C., & Meyer, R.-V. (26 June 2004). Preparation method of (co)oligomer or (co)polymer by in-situ polymerization of monoethylenically unsaturated monomer and oligomer or polymer secondary amine to control molecular weight and molecular structure. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (24 June 2004). In-situ polymerization of monoethylenically unsaturated monomers with secondary amines. |
Detrembleur, C., Rudiger, C., & Meyer, R.-V. (24 June 2004). Situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary amines. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (23 June 2004). In situ polymerization with monoethenoid unsaturation monomer of secondary amine. |
Detrembleur, C., Ruediger, C., & Meyer, R.-V. (23 June 2004). The in situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary amines. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (16 June 2004). In-situ polymerization of monoethylenically unsaturated monomers with secondary amines. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (16 June 2004). In-situ polymerization of monoethylenically unsaturated monomers with secondary amines. |
Detrembleur, C., Rüdiger, C., & Meyer, R.-V. (16 June 2004). The in-situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary amines. |
Meyer, R.-V., Gross, T., & Detrembleur, C. (13 June 2004). In-situ polymerization of monoethylenically unsaturated monomers with secondary amines. |
Meyer, R.-V., Rüdiger, C., & Detrembleur, C. (13 June 2004). The in situ polymerization of monoethylenically unsaturated monomers with oligomeric or polymeric secondary amines. |
Bertrand, O., Jérôme, R., Gautier, S., Maquet, V., Detrembleur, C., Jérôme, C., Voccia, S., Claes, M., Lou, X., & Labaye, D.-E. (09 June 2004). Process for depositing strong adherend polymer coating onto an electrically conductive surface. |
Vanhoorne, P., Meyer, R.-V., Detrembleur, C., & Jérôme, R. (18 May 2004). Controlled free-radical polymerization products using new controlled agents. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (08 April 2004). Method for producing functionalized alkoxyamine initiator and use thereof. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (04 March 2004). A process for the synthesis of alkoxyamines and their use in controlled radical polymerization. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (03 February 2004). Preparation of functionalized alkoxyamine initiator and its use. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (02 January 2004). One-pot process for the preparation of functionalized alkoxyamines. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (02 January 2004). A new process for the synthesis of alkoxyamines active in controlled radical polymerization. |
Detrembleur, C., Grob, T., & Meyer, R.-V. (01 January 2004). Process for the synthesis for alkoxy amines and their use in controlled radical polymerization. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (01 January 2004). Process for the synthesis for alkoxy amines and their use in controlled radical polymerization. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (25 December 2003). The preparation of functionalized alkoxyamine initiator and its use. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (25 December 2003). Preparation of functionalized alkoxyamine initiator and its use. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (25 December 2003). Preparation of functionalized alkoxyamine initiator and its use. |
Detrembleur, C., Gross, T., & Meyer, R.-V. (25 December 2003). A process for the synthesis of alkoxyamines and their use in controlled radical polymerization. |
Detrembleur, C., Lou, X., Voccia, S., Bertrand, O., Gautier, S., Maquet, V., Jérôme, C., Claes, M., Jérôme, R., & Labaye, D.-E. (16 December 2002). Process for depositing strong adherend polymer coating onto an electrically conductive surface. |
Bertrand, O., Jérôme, R., Gautier, S., Maquet, V., Detrembleur, C., Jérôme, C., Voccia, S., Claes, M., Lou, X., & Labaye, D.-E. (12 December 2002). Process for depositing strong adherend polymer coating onto an electrically conductive surface. |
Vanhoorne, P., Meyer, R.-V., Detrembleur, C., & Jérôme, R. (07 November 2002). Controlled free-radical polymerization products using new controlled agents. |
Jérôme, R., Meyer, R.-V., Vanhoorne, P., & Detrembleur, C. (12 September 2002). Controlled free-radical polymerization products using new controlled agents. |
VanHoorne, P., Meyer, R.-V., Detrembleur, C., & Jérôme, R. (06 September 2002). Controlled free-radical polymerization products using new controlled agents. |
Vanhoorne, P., Meyer, R.-V., Detrembleur, C., & Jérôme, R. (04 September 2002). Controlled free-radical polymerization products using new controlled agents. |
Jérôme, R., Creutz, S., Dubois, P., Detrembleur, C., & Lecomte, P. (23 April 1998). Method for controlled radical polymerization. |