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Shimomura, Y., Igawa, K., Sasaki, S., Sakakibara, N., Goseki, R. & Konishi, G.-I. (2022) Flexible Alkylene Bridges as a Tool To Engineer Crystal Distyrylbenzene Structures Enabling Highly Fluorescent Monomeric Emission. Chemistry – A European Journal, e202201884.
Added by: Richard Baschera (2022-08-19 07:03:21) Last edited by: Richard Baschera (2022-08-19 07:07:49) |
| Type de référence: Article DOI: 10.1002/chem.202201884 Numéro d'identification (ISBN etc.): 1521-3765 Clé BibTeX: Shimomura2022 Voir tous les détails bibliographiques  |
Catégories: INTERNATIONAL, PMN Mots-clés: aggregation-induced emission, crystal engineering, distyrylbenzene, organic light-emitting devices (OLEDs), solid state fluorescence Créateurs: Goseki, Igawa, Konishi, Sakakibara, Sasaki, Shimomura Collection: Chemistry – A European Journal |
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| Liens URLs https://onlinelibr ... 002/chem.202201884 |
| Résumé |
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To design ultrabright fluorescent solid dyes, a crystal engineering strategy that enables monomeric emission by blocking intermolecular electronic interactions is required. We introduced propylene moieties to distyrylbenzene (DSB) as bridges between the phenyl rings either side of its C=C bonds. The bridged DSB derivatives formed compact crystals that emit colors similar to those of the same molecules in dilute solution, with high quantum yields. The introduction of flexible seven-membered rings to the DSB core produced moderate distortion and steric hindrance in the DSB π-plane. However, owing to this strategy, it was possible to control the molecular arrangement with almost no decrease in the crystal density, and intermolecular electronic interactions were suppressed. The bridged DSB crystal structure differs from other DSB derivative structures; thus, bridging affords access to novel crystalline systems. This design strategy has important implications in many fields and is more effective than the conventional photofunctional molecular crystal design strategies.
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_eprint: https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202201884
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