Photoisomerization of an azobenzene on the Bi(111) surface
Modifying surface-bound molecular switches by adding side groups is an established concept for restoration of functionality which a molecule possesses in solution and which is often quenched upon adsorption. Instead of decoupling the photochromic unit from the substrate, we follow a different approa...
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| Autores principales: | , , , |
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| Formato: | Article (Journal) |
| Lenguaje: | inglés |
| Publicado: |
December 4, 2013
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| In: |
The journal of physical chemistry. C, Energy, materials, and catalysis
Year: 2013, Volumen: 117, Número: 51, Pages: 27031-27038 |
| ISSN: | 1932-7455 |
| DOI: | 10.1021/jp4106663 |
| Acceso en línea: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/jp4106663
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| Notas de Autor: | Christopher Bronner, Beate Priewisch, Karola Rück-Braun, and Petra Tegeder |
| Sumario: | Modifying surface-bound molecular switches by adding side groups is an established concept for restoration of functionality which a molecule possesses in solution and which is often quenched upon adsorption. Instead of decoupling the photochromic unit from the substrate, we follow a different approach, namely treating the complete molecule-substrate system. We use photoelectron spectroscopies to determine the energetic positions of the frontier orbitals of di-m-cyanoazobenzene on Bi(111) and to elucidate the isomerization mechanism which is stimulated by a substrate-mediated electron transfer process. |
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| Notas: | Gesehen am 08.12.2020 |
| Descripción Física: | Online Resource |
| ISSN: | 1932-7455 |
| DOI: | 10.1021/jp4106663 |