Parties d'ouvrages collectifs (2)
  1. 1. Berger, G., Wintjens, R., & Meyer, F. (2014). Preparation Of Racemic And Optically Active Trifluoromethyl Aziridines And Azetidines. In Targets In Heterocyclic Systems: Chemistry And Properties, Vol. 18. Reviews and Accounts on Heterocyclic Chemistry (1 ed., pp. 29-47). O. A. Attanasi, R. Noto and D. Spinelli, Italian Chemical Society and the Royal Society of Chemistry books.
  2. 2. Metrangolo, P., Meyer, F., Resnati, G., & Ursini, M. (2005). Haloperfluorocarbons: Versatile Tectons in Halogen Bonding Based Crystal Engineering. In V. Soloshonok (Ed.), Fluorine-containing synthon (p. 513). Washington, D.C: Oxford University Press/American Chemical Society.(ACS Symposium Series, 911).
    3.   Articles dans des revues avec comité de lecture (87)
  3. 1. Singh, A., Torres Huerta, A., Meyer, F., & Valkenier, H. (2024). Anion transporters based on halogen, chalcogen, and pnictogen bonds: towards biological applications. Chemical science. doi:10.1039/D4SC04644G
  4. 2. Frangville, P., Tanwar, A. S., Kumar, S., Gelbcke, M., Wauthoz, N., Basov, S., Van Bael, M. J., Van Hecke, K., & Meyer, F. (2024). Sensing diversity in halogen-bonded multi-stimuli responsive materials: Light, pH, magnetism, and electron-rich species. Materials Today Chemistry, 40, 102234. doi:10.1016/j.mtchem.2024.102234
  5. 3. Mbosso Teinkela, J. E., Oumarou, H., Siwe Noundou, X., Meyer, F., Megalizzi, V., Hoppe, H. H., Krause, R. W. M., & Wintjens, R. (2023). Evaluation of in vitro antiplasmodial, antiproliferative activities, and in vivo oral acute toxicity of Spathodea campanulata flowers. Scientific African, 21, e01871. doi:10.1016/j.sciaf.2023.e01871
  6. 4. Kumar, S., Van Hecke, K., & Meyer, F. (2023). Insight into Unusual Supramolecular Self-Assemblies of Terthiophenes Directed by Weak Hydrogen Bonding. International journal of molecular sciences, 24(13), 11127. doi:10.3390/ijms241311127
  7. 5. Vanheuverzwijn, J., Maillard, E.-E., Mahat, A., Fowler, L., Monteyne, D., Bonnaud, L., Landercy, N., Hemberg, A., Janković, A., Meyer, F., Mišković-Stanković, V., Stevanović, M., Mirica, C., Pérez-Morga, D., Luginbuehl, R., Combes, C., Furtos, G., & Fontaine, V. (2023). Easy, Flexible and Standardizable Anti-Nascent Biofilm Activity Assay to Assess Implant Materials. Microorganisms, 11(4), 1023. doi:10.3390/microorganisms11041023
  8. 6. Kumar, S., Body, C., Leyssens, T., Van Hecke, K., Berger, G., Van der Lee, A., Laurencin, D., Richeter, S., Clément, S., & Meyer, F. (2023). Halogen-Bonded Thiophene Derivatives Prepared by Solution and/or Mechanochemical Synthesis. Evidence of N···S Chalcogen Bonds in Homo- and Cocrystals. Crystal growth & design. doi:10.1021/acs.cgd.2c01402
  9. 7. Sow, I. S., Gelbcke, M., Meyer, F., Vandeput, M., Marloye, M., Basov, S., Van Bael, M., Berger, G., Robeyns, K., Hermans, S., Yang, D., Fontaine, V., & Dufrasne, F. (2023). Synthesis and biological activity of iron(II), iron(III), nickel(II), copper(II) and zinc(II) complexes of aliphatic hydroxamic acids. Journal of coordination chemistry, 1-30. doi:10.1080/00958972.2023.2166407
  10. 8. Al Nakib, R., Toncheva, A., Fontaine, V., Vanheuverzwijn, J., Raquez, J.-M., & Meyer, F. (2022). Design of Thermoplastic Polyurethanes with Conferred Antibacterial, Mechanical, and Cytotoxic Properties for Catheter Application. ACS Applied Bio Materials, 5(12), 5532-5544. doi:10.1021/acsabm.2c00531
  11. 9. Marloye, M., Inam, H., Moore, C. J., Mertens, T. R., Ingels, A., Koch, M., Nowicki, M. O., Mathieu, V., Pritchard, J. R., Awuah, S. G., Lawler, S. E., Meyer, F., Dufrasne, F., & Berger, G. (2022). Self-assembled ruthenium and osmium nanosystems display a potent anticancer profile by interfering with metabolic activity. Inorganic Chemistry Frontiers. doi:10.1039/D2QI00423B
  12. 10. Al Nakib, R., Toncheva, A., Fontaine, V., Vanheuverzwijn, J., Raquez, J.-M., & Meyer, F. (2022). Thermoplastic polyurethanes for biomedical application: A synthetic, mechanical, antibacterial, and cytotoxic study. Journal of applied polymer science, 139(4), 51666. doi:10.1002/app.51666
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