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Formation of Al<sub>4</sub>Cu<sub>9</sub> on the 5 fold surface of icosahedral AlPdMn
Bielmann, M., Barranco, A., Ruffieux, P., Gröning, O., Fasel, R., Widmer, R., & Gröning, P. (2005). Formation of Al4Cu9 on the 5 fold surface of icosahedral AlPdMn. Advanced Engineering Materials, 7(5), 392-396. https://doi.org/10.1002/adem.200500050
On-surface growth dynamics of graphene nanoribbons: the role of halogen functionalization
Di Giovannantonio, M., Deniz, O., Urgel, J. I., Widmer, R., Dienel, T., Stolz, S., Sánchez-Sánchez, C., Muntwiler, M., Dumslaff, T., Berger, R., Narita, A., Feng, X., Müllen, K., Ruffieux, P., & Fasel, R. (2018). On-surface growth dynamics of graphene nanoribbons: the role of halogen functionalization. ACS Nano, 12(1), 74-81. https://doi.org/10.1021/acsnano.7b07077
On-surface light-induced generation of higher acenes and elucidation of their open-shell character
Urgel, J. I., Mishra, S., Hayashi, H., Wilhelm, J., Pignedoli, C. A., Di Giovannantonio, M., Widmer, R., Yamashita, M., Hieda, N., Ruffieux, P., Yamada, H., & Fasel, R. (2019). On-surface light-induced generation of higher acenes and elucidation of their open-shell character. Nature Communications, 10(1), 861 (9 pp.). https://doi.org/10.1038/s41467-019-08650-y
On-surface synthesis and characterization of individual polyacetylene chains
Wang, S., Sun, Q., Gröning, O., Widmer, R., Pignedoli, C. A., Cai, L., Yu, X., Yuan, B., Li, C., Ju, H., Zhu, J., Ruffieux, P., Fasel, R., & Xu, W. (2019). On-surface synthesis and characterization of individual polyacetylene chains. Nature Chemistry, 11(10), 924-930. https://doi.org/10.1038/s41557-019-0316-8
On‐surface synthesis of cumulene‐like polymers via two‐step dehalogenative homocoupling of dibromomethylenes-functionalized tribenzoazulene
Urgel, J. I., Di Giovannantonio, M., Eimre, K., Lohr, T. G., Liu, J., Mishra, S., Sun, Q., Kinikar, A., Widmer, R., Stolz, S., Bommert, M., Berger, R., Ruffieux, P., Pignedoli, C. A., Müllen, K., Feng, X., & Fasel, R. (2020). On‐surface synthesis of cumulene‐like polymers via two‐step dehalogenative homocoupling of dibromomethylenes-functionalized tribenzoazulene. Angewandte Chemie International Edition, 59(32), 13281-13287. https://doi.org/10.1002/anie.202001939
Reversible dehalogenation in on-surface aryl-aryl coupling
Stolz, S., Di Giovannantonio, M., Urgel, J. I., Sun, Q., Kinikar, A., Borin Barin, G., Bommert, M., Fasel, R., & Widmer, R. (2020). Reversible dehalogenation in on-surface aryl-aryl coupling. Angewandte Chemie International Edition, 59(33), 1406-1410. https://doi.org/10.1002/anie.202005443
Surface science at the PEARL beamline of the Swiss Light Source
Muntwiler, M., Zhang, J., Stania, R., Matsui, F., Oberta, P., Flechsig, U., Patthey, L., Quitmann, C., Glatzel, T., Widmer, R., Meyer, E., Jung, T. A., Aebi, P., Fasel, R., & Greber, T. (2017). Surface science at the PEARL beamline of the Swiss Light Source. Journal of Synchrotron Radiation, 24(1), 354-366. https://doi.org/10.1107/S1600577516018646