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

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  • (-) Empa Authors ≠ Borin Barin, Gabriela
  • (-) Journal ≠ Applied Physics A: Materials Science and Processing
  • (-) Empa Authors = Urgel, José I.
Search Results 1 - 20 of 26
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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
On‐surface interchain coupling and skeletal rearrangement of indenofluorene polymers
Chen, Q., Di Giovannantonio, M., Eimre, K., Urgel, J. I., Ruffieux, P., Pignedoli, C. A., … Narita, A. (2023). On‐surface interchain coupling and skeletal rearrangement of indenofluorene polymers. Macromolecular Chemistry and Physics, 224(24), 2300345 (7 pp.). https://doi.org/10.1002/macp.202300345
On-surface synthesis and characterization of nitrogen-substituted undecacenes
Eimre, K., Urgel, J. I., Hayashi, H., Di Giovannantonio, M., Ruffieux, P., Sato, S., … Pignedoli, C. A. (2022). On-surface synthesis and characterization of nitrogen-substituted undecacenes. Nature Communications, 13, 511 (9 pp.). https://doi.org/10.1038/s41467-022-27961-1
On-surface polyarylene synthesis by cycloaromatization of isopropyl substituents
Kinikar, A., Di Giovannantonio, M., Urgel, J. I., Eimre, K., Qiu, Z., Gu, Y., … Fasel, R. (2022). On-surface polyarylene synthesis by cycloaromatization of isopropyl substituents. Nature Synthesis, 1, 289-296. https://doi.org/10.1038/s44160-022-00032-5
On-surface thermal stability of a graphenic structure incorporating a tropone moiety
Márquez, I. R., Ruíz del Árbol, N., Urgel, J. I., Villalobos, F., Fasel, R., López, M. F., … Sánchez-Sánchez, C. (2022). On-surface thermal stability of a graphenic structure incorporating a tropone moiety. Nanomaterials, 12(3), 488 (10 pp.). https://doi.org/10.3390/nano12030488
Efficient photogeneration of nonacene on nanostructured graphene
Ayani, C. G., Pisarra, M., Urgel, J. I., Navarro, J. J., Díaz, C., Hayashi, H., … Vázquez de Parga, A. L. (2021). Efficient photogeneration of nonacene on nanostructured graphene. Nanoscale Horizons, 6(9), 744-750. https://doi.org/10.1039/D1NH00184A
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 π-conjugated ladder-type polymers comprising nonbenzenoid moieties
Urgel, J. I., Bock, J., Di Giovannantonio, M., Ruffieux, P., Pignedoli, C. A., Kivala, M., & Fasel, R. (2021). On-surface synthesis of π-conjugated ladder-type polymers comprising nonbenzenoid moieties. RSC Advances, 11(38), 23437-23441. https://doi.org/10.1039/D1RA03253D
On-surface activation of benzylic C-H bonds for the synthesis of pentagon-fused graphene nanoribbons
Xu, X., Di Giovannantonio, M., Urgel, J. I., Pignedoli, C. A., Ruffieux, P., Müllen, K., … Narita, A. (2021). On-surface activation of benzylic C-H bonds for the synthesis of pentagon-fused graphene nanoribbons. Nano Research, 14, 4754-4759. https://doi.org/10.1007/s12274-021-3419-2
Large-cavity coronoids with different inner and outer edge structures
Di Giovannantonio, M., Yao, X., Eimre, K., Urgel, J. I., Ruffieux, P., Pignedoli, C. A., … Narita, A. (2020). Large-cavity coronoids with different inner and outer edge structures. Journal of the American Chemical Society, 142(28), 12046-12050. https://doi.org/10.1021/jacs.0c05268
On-surface dehydro-Diels–Alder reaction of dibromo-bis(phenylethynyl)benzene
Di Giovannantonio, M., Keerthi, A., Urgel, J. I., Baumgarten, M., Feng, X., Ruffieux, P., … Müllen, K. (2020). On-surface dehydro-Diels–Alder reaction of dibromo-bis(phenylethynyl)benzene. Journal of the American Chemical Society, 142(4), 1721-1725. https://doi.org/10.1021/jacs.9b11755
On-surface synthesis of oligo(indenoindene)
Di Giovannantonio, M., Chen, Q., Urgel, J. I., Ruffieux, P., Pignedoli, C. A., Müllen, K., … Fasel, R. (2020). On-surface synthesis of oligo(indenoindene). Journal of the American Chemical Society, 142(30), 12925-12929. https://doi.org/10.1021/jacs.0c05701
On-surface synthesis of unsaturated carbon nanostructures with regularly fused pentagon-heptagon pairs
Hou, I. C. Y., Sun, Q., Eimre, K., Di Giovannantonio, M., Urgel, J. I., Ruffieux, P., … Müllen, K. (2020). On-surface synthesis of unsaturated carbon nanostructures with regularly fused pentagon-heptagon pairs. Journal of the American Chemical Society, 142(23), 10291-10296. https://doi.org/10.1021/jacs.0c03635
On-surface synthesis of non-benzenoid nanographenes by oxidative ring-closure and ring-rearrangement reactions
Lohr, T. G., Urgel, J. I., Eimre, K., Liu, J., Di Giovannantonio, M., Mishra, S., … Feng, X. (2020). On-surface synthesis of non-benzenoid nanographenes by oxidative ring-closure and ring-rearrangement reactions. Journal of the American Chemical Society, 142(31), 13565-13572. https://doi.org/10.1021/jacs.0c05668
Topological defect-induced magnetism in a nanographene
Mishra, S., Beyer, D., Berger, R., Liu, J., Gröning, O., Urgel, J. I., … Fasel, R. (2020). Topological defect-induced magnetism in a nanographene. Journal of the American Chemical Society, 142(3), 1147-1152. https://doi.org/10.1021/jacs.9b09212
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
On-surface synthesis of antiaromatic and open-shell indeno[2,1-<em>b</em>]fluorene polymers and their lateral fusion into porous ribbons
Di Giovannantonio, M., Eimre, K., Yakutovich, A. V., Chen, Q., Mishra, S., Urgel, J. I., … Fasel, R. (2019). On-surface synthesis of antiaromatic and open-shell indeno[2,1-b]fluorene polymers and their lateral fusion into porous ribbons. Journal of the American Chemical Society, 141(31), 12346-12354. https://doi.org/10.1021/jacs.9b05335
Open-shell nonbenzenoid nanographenes containing two pairs of pentagonal and heptagonal rings
Liu, J., Mishra, S., Pignedoli, C. A., Passerone, D., Urgel, J. I., Fabrizio, A., … Feng, X. (2019). Open-shell nonbenzenoid nanographenes containing two pairs of pentagonal and heptagonal rings. Journal of the American Chemical Society, 141(30), 12011-12020. https://doi.org/10.1021/jacs.9b04718
Negatively curved warped nanographene self-assembled on metal surfaces
Urgel, J. I., Di Giovannantonio, M., Segawa, Y., Ruffieux, P., Scott, L. T., Pignedoli, C. A., … Fasel, R. (2019). Negatively curved warped nanographene self-assembled on metal surfaces. Journal of the American Chemical Society, 141(33), 13158-13164. https://doi.org/10.1021/jacs.9b05501
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., … 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