| DOI | Trouver le DOI : https://doi.org/10.1063/1.5079721 |
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| Auteur | Rechercher : Larsen, Martin A. B.; Rechercher : Sølling, Theis I.; Rechercher : Forbes, Ruaridh; Rechercher : Boguslavskiy, Andrey E.1; Rechercher : Makhija, Varun; Rechercher : Veyrinas, Kévin; Rechercher : Lausten, Rune1; Rechercher : Stolow, Albert1; Rechercher : Zawadzki, Magdalena M.; Rechercher : Saalbach, Lisa; Rechercher : Kotsina, Nikoleta; Rechercher : Paterson, Martin J.; Rechercher : Townsend, Dave |
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| Affiliation | - Conseil national de recherches du Canada. Technologies de sécurité et de rupture
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| Format | Texte, Article |
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| Résumé | Time-resolved photoelectron spectroscopy in combination with ab initio quantum chemistry calculations was used to study ultrafast excited state dynamics in formamide (FOR), N,N-dimethylformamide (DMF), and N,N-dimethylacetamide (DMA) following 160 nm excitation. The particular focus was on internal conversion processes within the excited state Rydberg manifold and on how this behavior in amides compared with previous observations in small amines. All three amides exhibited extremely rapid (<100 fs) evolution from the Franck–Condon region. We argue that this is then followed by dissociation. Our calculations indicate subtle differences in how the excited state dynamics are mediated in DMA/DMF as compared to FOR. We suggest that future studies employing longer pump laser wavelengths will be useful for discerning these differences. |
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| Date de publication | 2019-02-05 |
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| Maison d’édition | AIP Publishing |
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| Dans | |
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| Langue | anglais |
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| Publications évaluées par des pairs | Oui |
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| Exporter la notice | Exporter en format RIS |
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| Signaler une correction | Signaler une correction (s'ouvre dans un nouvel onglet) |
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| Identificateur de l’enregistrement | 26fa9441-8fea-4345-aedb-298cd5f99292 |
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| Enregistrement créé | 2019-06-10 |
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| Enregistrement modifié | 2020-03-16 |
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