Non-covalent graphene nanobuds from mono- and tripodal binding motifs
Graphene nanobuds were prepared via the non-covalent anchoring of C60-based molecules endowed with one or three pyrene units. TGA, FTIR, UV-Vis and TEM investigations confirmed the nanohybrids formation. For the two molecular derivatives, striking differences were determined in their interaction wit...
| Autores: | , , , , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2017 |
| País: | España |
| Institución: | Universidad Complutense de Madrid (UCM) |
| Repositorio: | Docta Complutense |
| Idioma: | inglés |
| OAI Identifier: | oai:docta.ucm.es:20.500.14352/18398 |
| Acceso en línea: | https://hdl.handle.net/20.500.14352/18398 |
| Access Level: | acceso abierto |
| Palabra clave: | 547 Química orgánica (Química) 2306 Química Orgánica |
| Sumario: | Graphene nanobuds were prepared via the non-covalent anchoring of C60-based molecules endowed with one or three pyrene units. TGA, FTIR, UV-Vis and TEM investigations confirmed the nanohybrids formation. For the two molecular derivatives, striking differences were determined in their interaction with graphene or carbon surfaces by Raman, cyclic voltammetry and molecular mechanics calculations, revealing the important role of pyrene adsorption in the electronic properties of the nanohybrids. |
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