Firealem G. Erko
Synthesis and photochromic properties of a bis(diarylethene)-naphthopyran hybrid
Erko, Firealem G.; Cseh, Liliana; Berthet, Jérôme; Mehl, Georg H.; Delbaere, Stéphanie
Authors
Liliana Cseh
Jérôme Berthet
Georg H. Mehl
Stéphanie Delbaere
Abstract
The synthesis and photochromic properties of a triphotochromic molecule consisting of one naphthopyran flanked by two diarylethene units investigated by UV-Visible and NMR spectroscopies are reported. Six different states resulting from the open/closed naphthopyran associated with one or two open/cyclized diarylethenes have been characterized. Switching of the naphthopyran group is possible, independently of the state of the diarylethene groups, permitting the controlled generation of electronically connected diarylethene groups. However, the diarylethene groups cannot be closed if the naphthopyran group is open.
Citation
Erko, F. G., Cseh, L., Berthet, J., Mehl, G. H., & Delbaere, S. (2015). Synthesis and photochromic properties of a bis(diarylethene)-naphthopyran hybrid. Dyes and pigments : an international journal, 115(April), 102-109. https://doi.org/10.1016/j.dyepig.2014.12.015
Journal Article Type | Article |
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Acceptance Date | Dec 16, 2014 |
Online Publication Date | Dec 31, 2014 |
Publication Date | 2015-04 |
Deposit Date | Sep 8, 2015 |
Publicly Available Date | Nov 23, 2017 |
Journal | Dyes and pigments |
Print ISSN | 0143-7208 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 115 |
Issue | April |
Pages | 102-109 |
DOI | https://doi.org/10.1016/j.dyepig.2014.12.015 |
Keywords | Photochromism; Naphthopyran; Diarylethene; UV-visible; NMR spectroscopy; Multi-switches |
Public URL | https://hull-repository.worktribe.com/output/378861 |
Publisher URL | http://www.sciencedirect.com/science/article/pii/S0143720814004690 |
Additional Information | Author's accepted manuscript of article which has been published in: Dyes and pigments, 2015, v.115 . |
Contract Date | Nov 23, 2017 |
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© 2016, Elsevier. Licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/
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