Stassen, Daphné, Demitri, Nicola and Bonifazi, Davide ![]() |
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Official URL: http://dx.doi.org/10.1002/anie.201509517
Abstract
The synthesis of O-doped benzorylenes, in which peripheral carbon atoms have been replaced by oxygen atoms, has been achieved for the first time. This includes key high-yielding ring-closure steps which, through intramolecular C−O bond formation, allow stepwise planarization of oligonaphthalenes. Single-crystal X-ray diffraction showed that the tetraoxa derivative forms remarkable face-to-face π–π stacks in the solid state, a favorable solid-state arrangement for organic electronics.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Schools > Chemistry |
Subjects: | Q Science > QD Chemistry |
Publisher: | Wiley-Blackwell |
ISSN: | 1433-7851 |
Funders: | ERC Project reference: 280183 |
Date of First Compliant Deposit: | 13 April 2016 |
Date of Acceptance: | 24 March 2016 |
Last Modified: | 06 Jan 2024 04:47 |
URI: | https://orca.cardiff.ac.uk/id/eprint/89195 |
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