Control of Local Ionization and Charge Transfer in the Bifunctional Molecule 2-Phenylethyl-N,N-dimethylamine Using Rydberg Fingerprint Spectroscopy
| Autor: | Narayanan Kuthirummal, Peter M. Weber, Wei Cheng, Rainer Weinkauf, Theis I. Sølling, Jaimie L. Gosselin |
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| Rok vydání: | 2005 |
| Předmět: | |
| Zdroj: | University of Copenhagen |
| ISSN: | 1520-5215 1089-5639 |
| DOI: | 10.1021/jp046400g |
| Popis: | Local photoionization pathways and charge-transfer dynamics of 2-phenylethyl-N,N-dimethylamine (PENNA) are explored using the recently developed Rydberg fingerprint spectroscopy. PENNA, a molecule that derives its biological significance from its relation to neurotransmitters, has two ionization centers that are separated by an ethyl group. We ionize the molecule in various multiphoton ionization processes using different laser wavelengths. The Rydberg fingerprint spectrum reveals the local nature of the ionization process and identifies the center of charge. We discovered that the laser wavelength provides substantial control over the activation of the individual ionization centers. The resonant (2+1) ionization with 400-nm radiation is dominated by the ejection of an electron from the amine moiety. In contrast, the resonant (1+1) ionization with 266-nm radiation leads predominantly to an ion with the charge in the phenyl group. The clean separation of the two ionization processes allows the exploration of ultrafast charge-transfer dynamics ensuing from a specific starting state characterized by a charged phenyl moiety. The width of the corresponding spectral features suggests that the charge transfer proceeds on a femtosecond time scale, suggesting a strong coupling between the two lowest-energy electronic surfaces of the PENNA cation. |
| Databáze: | OpenAIRE |
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