2017
DOI: 10.1039/c7tc01420a
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Tuning the self-assembly and photophysical properties of bi-1,3,4-thiadiazole derivatives through electron donor–acceptor interactions and their application in OLEDs

Abstract: Delicate interplay of donor–acceptor interactions in directing the self-assembly and its application.

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Cited by 45 publications
(27 citation statements)
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“…[ 43 ] The related thiadiazole‐based mesogens TIA‐3 were tested with respect to application in OLEDs as single emissive material or as guest in a polymeric host. [ 44 ] The host guest OLED devices clearly showed a higher efficiency and brightness of the blue emission. In this regard, a device consisting of poly(9‐vinylcarbazole) as host material with 5% of TIA‐3 (R 1 = R 2 = R 3 = OC 10 H 21 ) as emitting layer together with PVK:3T/10 (5 wt%) as the emitting layer together with bathocuproine (hole blocking layer) and tris‐(8‐hydroxyquinoline)aluminum (electron‐transporting layer) showed an external quantum efficiency of 0.63%.…”
Section: Synthetic Approachmentioning
confidence: 99%
“…[ 43 ] The related thiadiazole‐based mesogens TIA‐3 were tested with respect to application in OLEDs as single emissive material or as guest in a polymeric host. [ 44 ] The host guest OLED devices clearly showed a higher efficiency and brightness of the blue emission. In this regard, a device consisting of poly(9‐vinylcarbazole) as host material with 5% of TIA‐3 (R 1 = R 2 = R 3 = OC 10 H 21 ) as emitting layer together with PVK:3T/10 (5 wt%) as the emitting layer together with bathocuproine (hole blocking layer) and tris‐(8‐hydroxyquinoline)aluminum (electron‐transporting layer) showed an external quantum efficiency of 0.63%.…”
Section: Synthetic Approachmentioning
confidence: 99%
“…Because of their strong electron acceptability, they show attractive optical and electronic properties [24,25] . Similarly, there are many reports in the literature examining the remarkable properties of 1,3,4‐thiadiazole derivatives [26–31] . Especially, the substituted 1,3,4‐thiadiazole compounds have attracted increasingly significant attention due to their broad spectrum of pharmacological properties.…”
Section: Introductionmentioning
confidence: 99%
“…Hence, emitters were only incorporated in simple OLED structures which often required drive voltages >8 V and achieved a maximum luminance of mostly <1000 cd m −2 at voltages higher than 10 V, [27][28][29][30][31] similar to other studies of liquid crystal-based OLEDs. [17,[32][33][34][35] In order to develop more efficient liquid crystalline OLEDs, the knowledge about the self-assembling properties of DLCs that the community has acquired over the past decades needs to be appropriately integrated with state-of-the-art OLED structures and with the functional materials used in these.…”
Section: Introductionmentioning
confidence: 99%