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Résumé
The impact of intermolecular interactions on the third-order nonlinear optical (NLO) properties of open-shell molecular aggregates has been elucidated by considering one-dimensional aggregates of π-π stacked phenalenyl radicals with different intermolecular distances and the long-range corrected spin-unrestricted density functional theory method. In the phenalenyl dimer, which can be considered as a diradicaloid system, the diradical character strongly depends on the intermolecular distance, and the larger the intermolecular distance is, the larger the diradical character becomes. Then, around the equilibrium stacking distance that corresponds to an intermediate diradical character, its second hyperpolarizability (γ) is maximized and its value per monomer exhibits about a 30-fold enhancement with respect to the isolated phenalenyl monomer. This suggests that equilibrium is an optimal compromise between localization and delocalization of the radical electron pairs in such pancake bonding. No such effect was observed for the closed-shell coronene dimer. Moreover, when going from the dimer (diradical) to the tetramer (tetraradical), the γ-enhancement ratio increases nonlinearly with the aggregate size, whereas switching from the singlet to the highest spin (quintet) state causes a significant reduction of γ. Finally, for the tetramer, another one-order enhancement of γ is achieved for the dicationic singlet relative to its singlet neutral state. These results demonstrate the key role of intermolecular π-π stacking interactions and charge in open-shell (supra)molecular systems to achieve enhanced third-order NLO properties.
langue originale | Anglais |
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Pages (de - à) | 11129-11136 |
Nombre de pages | 8 |
journal | Chemistry: A European Journal |
Volume | 20 |
Numéro de publication | 35 |
Les DOIs | |
Etat de la publication | Publié - 25 août 2014 |
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Examiner les sujets de recherche de « Third-order nonlinear optical properties of one-dimensional open-shell molecular aggregates composed of phenalenyl radicals ». Ensemble, ils forment une empreinte digitale unique.Projets
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PAI n°P7/05 - FS2: Systèmes supramoléculaires fonctionnels (PAI P7/05)
CHAMPAGNE, B. (Co-investigateur), De Vos, D. (Responsable du Projet), Van der Auweraer, M. (Co-investigateur), Jérôme, C. (Co-investigateur), Lazzaroni, R. (Co-investigateur), Marin, G. (Co-investigateur), Jonas, A. (Co-investigateur), Du Prez, F. (Co-investigateur), Vanderzande, D. (Co-investigateur), Van Tendeloo, G. (Co-investigateur), Van Speybroeck, V. (Co-investigateur), NENON, S. (Chercheur) & STAELENS, N. (Chercheur)
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consortium des équipements de calcul intensif
Champagne, B. (Co-investigateur)
1/01/11 → 31/12/22
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TINTIN - ARC 09/14-23: Molecular TINkertoys for OpToelectronics and SpINtronics - TINTIN
BONIFAZI, D. (Responsable du Projet), CHAMPAGNE, B. (Co-investigateur), FORENSI, S. (Chercheur), SEGERIE, A. (Chercheur) & Melinte, S. (Co-investigateur)
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Projet: Recherche
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Plateforme Technologique Calcul Intensif
Champagne, B. (!!Manager)
Plateforme technologique Calcul intensifEquipement/installations: Plateforme technolgique