Kuss-Petermann, Martin and Wenger, Oliver S.. (2017) Exceptionally Long-Lived Photodriven Multi-Electron Storage without Sacrificial Reagents. Chemistry - A European Journal, 23 (45). pp. 10808-10814.
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Official URL: http://edoc.unibas.ch/58020/
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Abstract
Photoexcitation of a molecular pentad in the presence of Sc3+ in de-aerated CH3CN leads to a quinone dianion that is stable on the millisecond timescale. Light-driven electron accumulation on the quinone unit is sensitized by two Ru(bpy)32+ complexes in an intramolecular process, which relies on covalently attached triarylamine donors rather than on sacrificial reagents. Lewis acid–Lewis base interactions between Sc3+ and quinone dianion are responsible for the exceptionally long lifetime of this photoproduct. Our study of photoinduced multi-electron transfer is relevant in the greater context of solar energy conversion.
Faculties and Departments: | 05 Faculty of Science > Departement Chemie > Chemie > Anorganische Chemie (Wenger) |
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UniBasel Contributors: | Wenger, Oliver and Kuss-Petermann, Martin |
Item Type: | Article, refereed |
Article Subtype: | Research Article |
Publisher: | Wiley |
ISSN: | 0947-6539 |
e-ISSN: | 1521-3765 |
Note: | Publication type according to Uni Basel Research Database: Journal article |
Identification Number: | |
Last Modified: | 27 Dec 2017 13:59 |
Deposited On: | 27 Dec 2017 13:59 |
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