Nonacene generated by on-surface dehydrogenation
The on-surface synthesis of nonacene has been accomplished by dehydrogenation of an air-stable partially saturated precursor, which could be aromatized by using a combined scanning tunnelling and atomic force microscope (STM/AFM) tip as well as by on-surface annealing. This transformation allowed th...
| Autores: | , , , , , , , |
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| Tipo de documento: | artigo |
| Estado: | Versión aceptada para publicación |
| Data de publicação: | 2017 |
| País: | España |
| Recursos: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositório: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:2072/335515 |
| Acesso em linha: | http://hdl.handle.net/2072/335515 https://doi.org/10.1021/acsnano.7b04728 |
| Access Level: | Acceso aberto |
| Palavra-chave: | 54 |
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Nonacene generated by on-surface dehydrogenationZuzak, RafalDorel, RuthKrawiec, MariuszSuch, BartoszKolmer, MarekSzymonski, MarekEchavarren, Antonio M.Godlewski, Szymon54The on-surface synthesis of nonacene has been accomplished by dehydrogenation of an air-stable partially saturated precursor, which could be aromatized by using a combined scanning tunnelling and atomic force microscope (STM/AFM) tip as well as by on-surface annealing. This transformation allowed the in-detail analysis of the electronic properties of nonacene molecules physisorbed on Au(111) by scanning tunnelling spectroscopy (STS) measurements, which were corroborated by density theory functional (DFT) calculations thus confirming the spatial mapping of its molecular orbitals. Furthermore, the thermally-induced dehydrogenation uncovered the isomerisation of intermediate dihydrononacene species, which allowed for their in-depth structural and electronic characterization.2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersion9321 p.application/pdfhttp://hdl.handle.net/2072/335515https://doi.org/10.1021/acsnano.7b04728RECERCAT (Dipòsit de la Recerca de Catalunya)reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésL'accés als continguts d'aquest document queda condicionat a l'acceptació de les condicions d'ús establertes per la següent llicència Creative Commons:http://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessoai:recercat.cat:2072/3355152026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
Nonacene generated by on-surface dehydrogenation |
| title |
Nonacene generated by on-surface dehydrogenation |
| spellingShingle |
Nonacene generated by on-surface dehydrogenation Zuzak, Rafal 54 |
| title_short |
Nonacene generated by on-surface dehydrogenation |
| title_full |
Nonacene generated by on-surface dehydrogenation |
| title_fullStr |
Nonacene generated by on-surface dehydrogenation |
| title_full_unstemmed |
Nonacene generated by on-surface dehydrogenation |
| title_sort |
Nonacene generated by on-surface dehydrogenation |
| dc.creator.none.fl_str_mv |
Zuzak, Rafal Dorel, Ruth Krawiec, Mariusz Such, Bartosz Kolmer, Marek Szymonski, Marek Echavarren, Antonio M. Godlewski, Szymon |
| author |
Zuzak, Rafal |
| author_facet |
Zuzak, Rafal Dorel, Ruth Krawiec, Mariusz Such, Bartosz Kolmer, Marek Szymonski, Marek Echavarren, Antonio M. Godlewski, Szymon |
| author_role |
author |
| author2 |
Dorel, Ruth Krawiec, Mariusz Such, Bartosz Kolmer, Marek Szymonski, Marek Echavarren, Antonio M. Godlewski, Szymon |
| author2_role |
author author author author author author author |
| dc.subject.none.fl_str_mv |
54 |
| topic |
54 |
| description |
The on-surface synthesis of nonacene has been accomplished by dehydrogenation of an air-stable partially saturated precursor, which could be aromatized by using a combined scanning tunnelling and atomic force microscope (STM/AFM) tip as well as by on-surface annealing. This transformation allowed the in-detail analysis of the electronic properties of nonacene molecules physisorbed on Au(111) by scanning tunnelling spectroscopy (STS) measurements, which were corroborated by density theory functional (DFT) calculations thus confirming the spatial mapping of its molecular orbitals. Furthermore, the thermally-induced dehydrogenation uncovered the isomerisation of intermediate dihydrononacene species, which allowed for their in-depth structural and electronic characterization. |
| publishDate |
2017 |
| dc.date.none.fl_str_mv |
2017 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion |
| format |
article |
| status_str |
acceptedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/2072/335515 https://doi.org/10.1021/acsnano.7b04728 |
| url |
http://hdl.handle.net/2072/335515 https://doi.org/10.1021/acsnano.7b04728 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
9321 p. application/pdf |
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Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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Recercat. Dipósit de la Recerca de Catalunya |
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1869421873850220544 |
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15.812455 |