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  • (-) (Author:(Fasel) OR Co-Author:(Fasel))

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  • (-) Empa Authors = Widmer, Roland
  • (-) Journal ≠ Journal of the American Chemical Society
  • (-) Journal ≠ Journal of Synchrotron Radiation
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  • (-) Keywords ≠ reaction kinetics
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Growth optimization and device integration of narrow‐bandgap graphene nanoribbons
Borin Barin, G., Sun, Q., Di Giovannantonio, M., Du, C. ‐Z., Wang, X. ‐Y., Llinas, J. P., … Ruffieux, P. (2022). Growth optimization and device integration of narrow‐bandgap graphene nanoribbons. Small, 18(31), 2202301 (10 pp.). https://doi.org/10.1002/smll.202202301
On-surface synthesis of organocopper metallacycles through activation of inner diacetylene moieties 
Cirera, B., Riss, A., Mutombo, P., Urgel, J. I., Santos, J., Di Giovannantonio, M., … Écija, D. (2021). On-surface synthesis of organocopper metallacycles through activation of inner diacetylene moieties . Chemical Science, 12(38), 12806-12811. https://doi.org/10.1039/D1SC03703J
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., … 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., … 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
Sterically selective [3 + 3] cycloaromatization in the on-surface synthesis of nanographenes
Kinikar, A., Wang, X. Y., Di Giovannantonio, M., Urgel, J. I., Liu, P., Eimre, K., … Fasel, R. (2024). Sterically selective [3 + 3] cycloaromatization in the on-surface synthesis of nanographenes. ACS Nanoscience Au. https://doi.org/10.1021/acsnanoscienceau.3c00062