Articles dans des revues avec comité de lecture (223)
  1. 94. Thankaraj Salammal, S., Balandier, J.-Y., Kumar, S., Goormaghtigh, E., & Geerts, Y. (2014). Influence of Solubilizing Group Removal Rate on the Morphology and Crystallinity of a Diketopyrrolopyrrole-Based Compound. Crystal growth & design, 14, 339.
  2. 95. Dohr, M., Werzer, O., Shen, Q., Salzmann, I., Teichert, C., Ruzié, C., Schweicher, G., Geerts, Y., Sferrazza, M., & Resel, R. (2013). Dynamics of Monolayer–Island Transitions in 2,7-Dioctyl-benzothienobenzthiophene Thin Films. ChemPhysChem, 14(11), 2554–2559. doi:10.1002/cphc.201300227
  3. 96. Ruzié, C., Karpinska, J., Kennedy, A. R., & Geerts, Y. (2013). Synthesis of 1,6-, 2,7-, 3,8-, and 4,9-isomers of didodecyl[1] benzothieno[3,2-b][1]benzothiophenes. Journal of organic chemistry, 78(15), 7741-7748. doi:10.1021/jo401134c
  4. 97. Stas, S., Balandier, J.-Y., Lemaur, V., Fenwick, O., Tregnago, G., Quist, F., Cacialli, F., Cornil, J., & Geerts, Y. (2013). Straightforward access to diketopyrrolopyrrole (DPP) dimers. Dyes and pigments, 97(1), 198-208. doi:10.1016/j.dyepig.2012.12.005
  5. 98. Stas, S., Balandier, J.-Y., Lemaur, V., Fenwick, O., Tregnago, G., Quist, F., Cacialli, F., Cornil, J., & Geerts, Y. (2013). Straightforward access to diketopyrrolopyrrole dimers. Dyes and pigments, 97(1), 198-208.
  6. 99. George, Z., Kroon, R., Gehlhaar, R., Gbabode, G., Lundin, A., Hellstrom, S., Muller, C., Geerts, Y., Heremans, P., & Andersson, M. (2013). The influence of alkoxy substitutions on the properties of diketopyrrolopyrrole-phenyl copolymers for solar cells. Materials evaluation, 6(3022).
  7. 100. Ruzié, C., Karpinska, J., Kennedy, A., & Geerts, Y. (2013). Synthesis of 1,6-,2,7-,3,8-,and 4,9-isomers of didodecyl [1]benzothiophenes. Journal of organic chemistry, 78, 7741.
  8. 101. Méndez, H., Heimel, G., Opitz, A., Sauer, K., Barkowski, P., Oehzelt, M., Soeda, J., Okamoto, T., Takeya, J., Arlin, J.-B., Balandier, J.-Y., Geerts, Y., Koch, N., & Salzmann, I. (2013). Doping of organic semiconductors : Impact of dopant strength and electronic coupling. Angewandte Chemie, 125, 7905. doi:10.1002/anie.201302396
  9. 102. Boon, F., Hergue, N., Deshayes, G., Moerman, D., Desbief, S., De Winter, J., Gerbaux, P., Geerts, Y., & Dubois, P. (2013). Synthesis of poly[(4,40-(dihexyl)dithieno(3,2-b;20,30-d)- silole)] and copolymerization with 3-hexylthiophene: new semiconducting materials with extended optical absorption. Polymer Chemistry, 4, 4303.
  10. 103. George, Z., Kroon, R., Gehlhaar, R., Gbabode, G., Lundin, A., Hellstrom, S., Muller, C., Geerts, Y., Heremans, P., & Andersson, M. (2013). The Influence of Alkoxy Substitutions on the Properties of Diketopyrrolopyrrole-Phenyl Copolymers for Solar Cells. Materials, 6, 3022.
  11. 104. Ruzié, C., Karpinska, J., Kennedy, A., & Geerts, Y. (2013). Synthesis of 1,6‑, 2,7‑, 3,8‑, and 4,9-Isomers of Didodecyl[1]benzothieno[3,2‑b][1]benzothiophenes. Journal of organic chemistry, 78, 7741.
  12. 105. Afsharimani, N., Minoia, A., Volcke, C., Surin, M., Lazzaroni, R., Balandier, J.-Y., Niebel, C., Geerts, Y., & Nysten, B. (2013). Self-Assembly of Alkyl-Substituted Oligothiophenes on MoS2: A Joint Experimental/Theoretical Study. The Journal of Physical Chemistry Part C: Nanomaterials and Interfaces, 117, 21743.
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