Energy transfer from a rhodamine antenna to a ruthenium-bipyridine center
The coordination of a modified rhodamine B (Rhod) to a bis-bipyridine ruthenium (ii) (Ru-bpy) phototrigger complex enables a photodissociation reaction at longer wavelengths through enhanced absorption of green light (532 nm). The very high molar absorptivity of rhodamine (∼105 M -1 cm-1) and the hi...
| Autores: | , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2012 |
| País: | Argentina |
| Institución: | Consejo Nacional de Investigaciones Científicas y Técnicas |
| Repositorio: | CONICET Digital (CONICET) |
| Idioma: | inglés |
| OAI Identifier: | oai:ri.conicet.gov.ar:11336/70916 |
| Acceso en línea: | http://hdl.handle.net/11336/70916 |
| Access Level: | acceso abierto |
| Palabra clave: | Fret Caged Nitrile Ruthenium https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| Sumario: | The coordination of a modified rhodamine B (Rhod) to a bis-bipyridine ruthenium (ii) (Ru-bpy) phototrigger complex enables a photodissociation reaction at longer wavelengths through enhanced absorption of green light (532 nm). The very high molar absorptivity of rhodamine (∼105 M -1 cm-1) and the high quantum efficiency of Förster resonance energy transfer (FRET) from rhodamine to the Ru-bpy center (0.84) result in an unusually high photosensitivity and uncaging cross-section of the Ru-bpy-rhodamine complex at longer wavelengths. |
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