Hempe, Matthias ; Paschek, Johanna ; Schelter, Jürgen ; Umbach, Anne ; Meerholz, Klaus ; Reggelin, Michael (2020)
Crosslinkable bis(diphenylamine)‐substituted mixed dihydroindeno[1,2‐b]fluorenes for solution‐processed multilayer organic light‐emitting diodes.
In: ChemPlusChem, 85 (1)
doi: 10.1002/cplu.201900528
Artikel, Bibliographie
Dies ist die neueste Version dieses Eintrags.
Kurzbeschreibung (Abstract)
The synthesis and application of a series of crosslinkable bis(diphenylamine)‐substituted mixed dihydroindeno[1,2‐b]fluorenes as model systems for the fabrication of solution‐processed, multilayer organic light‐emitting diodes (OLEDs) is described. Introducing a novel functionalization approach by C(sp³)−C(sp²) Suzuki‐Miyaura reactions, the synthesis is based on a modular strategy, leading to eight nearly isoelectronic derivatives that allow for the observation of structure‐property relationships in the context of crosslinkable hole‐transport materials, e. g., for use in OLEDs. By systematically altering structural parameters, such as the number of crosslinkable oxetane moieties per molecule (2–6 moieties) and their position of attachment (geminal and/or lateral), process‐relevant thermal properties such as thermal stability (Td95, 170‐350°C) and glass‐transition temperature (15‐100°C) can be influenced and allow for the investigation of their impact on the crosslinking behavior and the resulting device performance.
Typ des Eintrags: | Artikel | ||||
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Erschienen: | 2020 | ||||
Autor(en): | Hempe, Matthias ; Paschek, Johanna ; Schelter, Jürgen ; Umbach, Anne ; Meerholz, Klaus ; Reggelin, Michael | ||||
Art des Eintrags: | Bibliographie | ||||
Titel: | Crosslinkable bis(diphenylamine)‐substituted mixed dihydroindeno[1,2‐b]fluorenes for solution‐processed multilayer organic light‐emitting diodes | ||||
Sprache: | Englisch | ||||
Publikationsjahr: | 2020 | ||||
Ort: | Weinheim | ||||
Verlag: | Wiley-VCH | ||||
Titel der Zeitschrift, Zeitung oder Schriftenreihe: | ChemPlusChem | ||||
Jahrgang/Volume einer Zeitschrift: | 85 | ||||
(Heft-)Nummer: | 1 | ||||
DOI: | 10.1002/cplu.201900528 | ||||
Zugehörige Links: | |||||
Kurzbeschreibung (Abstract): | The synthesis and application of a series of crosslinkable bis(diphenylamine)‐substituted mixed dihydroindeno[1,2‐b]fluorenes as model systems for the fabrication of solution‐processed, multilayer organic light‐emitting diodes (OLEDs) is described. Introducing a novel functionalization approach by C(sp³)−C(sp²) Suzuki‐Miyaura reactions, the synthesis is based on a modular strategy, leading to eight nearly isoelectronic derivatives that allow for the observation of structure‐property relationships in the context of crosslinkable hole‐transport materials, e. g., for use in OLEDs. By systematically altering structural parameters, such as the number of crosslinkable oxetane moieties per molecule (2–6 moieties) and their position of attachment (geminal and/or lateral), process‐relevant thermal properties such as thermal stability (Td95, 170‐350°C) and glass‐transition temperature (15‐100°C) can be influenced and allow for the investigation of their impact on the crosslinking behavior and the resulting device performance. |
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Alternatives oder übersetztes Abstract: |
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Freie Schlagworte: | crosslinking, materials science, OLEDs, oxetanes, polymerization | ||||
Sachgruppe der Dewey Dezimalklassifikatin (DDC): | 500 Naturwissenschaften und Mathematik > 540 Chemie | ||||
Fachbereich(e)/-gebiet(e): | 07 Fachbereich Chemie 07 Fachbereich Chemie > Clemens-Schöpf-Institut 07 Fachbereich Chemie > Clemens-Schöpf-Institut > Fachgebiet Organische Chemie |
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Hinterlegungsdatum: | 31 Jan 2024 07:46 | ||||
Letzte Änderung: | 31 Jan 2024 07:46 | ||||
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Verfügbare Versionen dieses Eintrags
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Crosslinkable Bis(diphenylamine)‐Substituted Mixed Dihydroindeno[1,2‐b]fluorenes for Solution‐Processed Multilayer Organic Light‐Emitting Diodes. (deposited 30 Jan 2024 13:40)
- Crosslinkable bis(diphenylamine)‐substituted mixed dihydroindeno[1,2‐b]fluorenes for solution‐processed multilayer organic light‐emitting diodes. (deposited 31 Jan 2024 07:46) [Gegenwärtig angezeigt]
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