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      Nonvolatile liquid anthracenes for facile full-colour luminescence tuning at single blue-light excitation

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          Abstract

          Nonvolatile room-temperature luminescent molecular liquids are a new generation of organic soft materials. They possess high stability, versatile optical properties, solvent-free fluid behaviour and can effectively accommodate dopant dye molecules. Here we introduce an approach to optimize anthracene-based liquid materials, focussing on enhanced stability, fluorescence quantum yield, colour tunability and processability, with a view to flexible electronic applications. Enveloping the anthracene core in low-viscosity branched aliphatic chains results in stable, nonvolatile, emissive liquid materials. Up to 96% efficient energy-transfer-assisted tunable emission is achieved by doping a minute amount of acceptor dye in the solvent-free state. Furthermore, we use a thermoresponsive dopant to impart thermally controllable luminescence colours. The introduced strategy leading to diverse luminescence colours at a single blue-light excitation can be an innovative replacement for currently used luminescent materials, providing useful continuous emissive layers in developing foldable devices.

          Abstract

          Nonvolatile luminescent liquids are solvent-free fluids with a range of flexible electronic applications. Here, the authors show that anthracenes enveloped in branched aliphatic compounds are stable emissive liquids, with emissive and thermoresponsive properties that may be tuned by addition of dopants.

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          Most cited references15

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          A luminescent mixed-lanthanide metal-organic framework thermometer.

          A luminescent mixed lanthanide metal-organic framework approach has been realized to explore luminescent thermometers. The targeted self-referencing luminescent thermometer Eu(0.0069)Tb(0.9931)-DMBDC (DMBDC = 2, 5-dimethoxy-1, 4-benzenedicarboxylate) based on two emissions of Tb(3+) at 545 nm and Eu(3+) at 613 nm is not only more robust, reliable, and instantaneous but also has higher sensitivity than the parent MOF Tb-DMBDC based on one emission at a wide range from 10 to 300 K. © 2012 American Chemical Society
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            Graphene as transparent electrode material for organic electronics.

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              Vesicular perylene dye nanocapsules as supramolecular fluorescent pH sensor systems.

              Water-soluble, self-assembled nanocapsules composed of a functional bilayer membrane and enclosed guest molecules can provide smart (that is, condition responsive) sensors for a variety of purposes. Owing to their outstanding optical and redox properties, perylene bisimide chromophores are interesting building blocks for a functional bilayer membrane in a water environment. Here, we report water-soluble perylene bisimide vesicles loaded with bispyrene-based energy donors in their aqueous interior. These loaded vesicles are stabilized by in situ photopolymerization to give nanocapsules that are stable over the entire aqueous pH range. On the basis of pH-tunable spectral overlap of donors and acceptors, the donor-loaded polymerized vesicles display pH-dependent fluorescence resonance energy transfer from the encapsulated donors to the bilayer dye membrane, providing ultrasensitive pH information on their aqueous environment with fluorescence colour changes covering the whole visible light range. At pH 9.0, quite exceptional white fluorescence could be observed for such water-soluble donor-loaded perylene vesicles.
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                Author and article information

                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Pub. Group
                2041-1723
                05 June 2013
                : 4
                : 1969
                Affiliations
                [1 ]National Institute for Materials Science (NIMS) , 1-2-1 Sengen, Tsukuba 305-0047, Japan
                [2 ]Department of Applied Chemistry, Graduate School of Engineering, Osaka University , Osaka 565-0871, Japan
                [3 ]Department of Chemistry, Faculty of Science, Shizuoka University , 836 Ohya, Suruga-ku, Shizuoka 422-8529, Japan
                [4 ]Chemical Resources Laboratory, Tokyo Institute of Technology , Yokohama 226-8503, Japan
                [5 ]Department of Interfaces, Max Planck Institute of Colloids and Interfaces, Research Campus Golm , Potsdam 14476, Germany
                Author notes
                Article
                ncomms2969
                10.1038/ncomms2969
                3709479
                23736114
                e5936734-7de8-4c28-a24c-a28524792ca3
                Copyright © 2013, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.

                This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. To view a copy of this licence visit http://creativecommons.org/licenses/by/3.0/.

                History
                : 07 January 2013
                : 02 May 2013
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