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New [1]benzothieno[3,2-]benzothiophene-tetraoxide-based TADF emitters with a D-A-D structure for OLED applications

Luminescent organic molecules showing thermally activated delayed fluorescence (TADF) are appealing materials for high-efficiency OLEDs. Here, we report a new class of organic luminescent materials with TADF properties, and a D-A-D electronic structure based on [1]benzothieno[3,2- b ]benzothiophene-...

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Published in:Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2025-01, Vol.13 (1), p.16-176
Main Authors: Montrone, Maria, Maggiore, Antonio, Moliterni, Anna, Pander, Piotr, Pugliese, Marco, Capodilupo, Agostina Lina, Gambino, Salvatore, Prontera, Carmela Tania, Valenzano, Vitantonio, Mariano, Fabrizio, Accorsi, Gianluca, Sibillano, Teresa, Giannini, Cinzia, Gigli, Giuseppe, Cardone, Antonio, Maiorano, Vincenzo
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container_title Journal of materials chemistry. C, Materials for optical and electronic devices
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creator Montrone, Maria
Maggiore, Antonio
Moliterni, Anna
Pander, Piotr
Pugliese, Marco
Capodilupo, Agostina Lina
Gambino, Salvatore
Prontera, Carmela Tania
Valenzano, Vitantonio
Mariano, Fabrizio
Accorsi, Gianluca
Sibillano, Teresa
Giannini, Cinzia
Gigli, Giuseppe
Cardone, Antonio
Maiorano, Vincenzo
description Luminescent organic molecules showing thermally activated delayed fluorescence (TADF) are appealing materials for high-efficiency OLEDs. Here, we report a new class of organic luminescent materials with TADF properties, and a D-A-D electronic structure based on [1]benzothieno[3,2- b ]benzothiophene-tetraoxide BTBTOx 4 as the acceptor unit A. Three donor units D were selected and coupled with BTBTOx 4 , using a straightforward synthetic protocol based on microwave-assisted Buchwald-Hartwig cross-coupling, to yield three organic luminescent molecules labelled PTz 2 -BTBTOx 4 , MPA 2 -BTBTOx 4 and POCz 2 -BTBTOx 4 . Chemico-physical and structural properties were investigated by cyclic voltammetry, electrical measurements, crystallographic analysis, theoretical study and photophysical characterization. All three emitters showed high electrochemical stability with reversible oxidation waves. MPA 2 -BTBTOx 4 was selected as the reference molecule for X-ray analysis, which revealed torsion angles of −59° and 86° between the donor (MPA) and acceptor (BTBTOx 4 ) units supporting their appropriate structural configuration to have TADF properties. Photophysical studies highlighted a noteworthy increase in PL efficiency upon deoxygenation for all three compounds. The oxygen-induced quenching of delayed fluorescence and time-resolved photoluminescence studies supported the presence of the TADF properties, further corroborated for PTz 2 -BTBTOx 4 and MPA 2 -BTBTOx 4 by DFT studies. Preliminary steady-state photophysical studies were also carried out on neat films of all three emitters, revealing a pronounced self-quenching of photoluminescence for PTz 2 -BTBTOx 4 and MPA 2 -BTBTOx 4 and a minimal self-quenching for POCz 2 -BTBTOx 4 , which maintains a high Φ PL (22%) comparable to that in Zeonex and half of that in PMMA. As a proof of concept, the three emitting molecules were tested as neat films in simple-structure OLED devices. In accordance with the photoluminescence data, POCz 2 -BTBTOx 4 , thanks to its sterically bulky structure, retains a good emission capacity even in a neat film and was also selected as an active matrix to build OLED devices by using two different deposition techniques: inkjet-printing and spin coating. [1]Benzothieno[3,2- b ]benzothiophene as a straightforward electron-acceptor building block to fabricate thermally activated delayed fluorescence (TADF) emitters.
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Here, we report a new class of organic luminescent materials with TADF properties, and a D-A-D electronic structure based on [1]benzothieno[3,2- b ]benzothiophene-tetraoxide BTBTOx 4 as the acceptor unit A. Three donor units D were selected and coupled with BTBTOx 4 , using a straightforward synthetic protocol based on microwave-assisted Buchwald-Hartwig cross-coupling, to yield three organic luminescent molecules labelled PTz 2 -BTBTOx 4 , MPA 2 -BTBTOx 4 and POCz 2 -BTBTOx 4 . Chemico-physical and structural properties were investigated by cyclic voltammetry, electrical measurements, crystallographic analysis, theoretical study and photophysical characterization. All three emitters showed high electrochemical stability with reversible oxidation waves. MPA 2 -BTBTOx 4 was selected as the reference molecule for X-ray analysis, which revealed torsion angles of −59° and 86° between the donor (MPA) and acceptor (BTBTOx 4 ) units supporting their appropriate structural configuration to have TADF properties. Photophysical studies highlighted a noteworthy increase in PL efficiency upon deoxygenation for all three compounds. The oxygen-induced quenching of delayed fluorescence and time-resolved photoluminescence studies supported the presence of the TADF properties, further corroborated for PTz 2 -BTBTOx 4 and MPA 2 -BTBTOx 4 by DFT studies. Preliminary steady-state photophysical studies were also carried out on neat films of all three emitters, revealing a pronounced self-quenching of photoluminescence for PTz 2 -BTBTOx 4 and MPA 2 -BTBTOx 4 and a minimal self-quenching for POCz 2 -BTBTOx 4 , which maintains a high Φ PL (22%) comparable to that in Zeonex and half of that in PMMA. 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C, Materials for optical and electronic devices</title><description>Luminescent organic molecules showing thermally activated delayed fluorescence (TADF) are appealing materials for high-efficiency OLEDs. Here, we report a new class of organic luminescent materials with TADF properties, and a D-A-D electronic structure based on [1]benzothieno[3,2- b ]benzothiophene-tetraoxide BTBTOx 4 as the acceptor unit A. Three donor units D were selected and coupled with BTBTOx 4 , using a straightforward synthetic protocol based on microwave-assisted Buchwald-Hartwig cross-coupling, to yield three organic luminescent molecules labelled PTz 2 -BTBTOx 4 , MPA 2 -BTBTOx 4 and POCz 2 -BTBTOx 4 . Chemico-physical and structural properties were investigated by cyclic voltammetry, electrical measurements, crystallographic analysis, theoretical study and photophysical characterization. All three emitters showed high electrochemical stability with reversible oxidation waves. MPA 2 -BTBTOx 4 was selected as the reference molecule for X-ray analysis, which revealed torsion angles of −59° and 86° between the donor (MPA) and acceptor (BTBTOx 4 ) units supporting their appropriate structural configuration to have TADF properties. Photophysical studies highlighted a noteworthy increase in PL efficiency upon deoxygenation for all three compounds. The oxygen-induced quenching of delayed fluorescence and time-resolved photoluminescence studies supported the presence of the TADF properties, further corroborated for PTz 2 -BTBTOx 4 and MPA 2 -BTBTOx 4 by DFT studies. Preliminary steady-state photophysical studies were also carried out on neat films of all three emitters, revealing a pronounced self-quenching of photoluminescence for PTz 2 -BTBTOx 4 and MPA 2 -BTBTOx 4 and a minimal self-quenching for POCz 2 -BTBTOx 4 , which maintains a high Φ PL (22%) comparable to that in Zeonex and half of that in PMMA. 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Chemico-physical and structural properties were investigated by cyclic voltammetry, electrical measurements, crystallographic analysis, theoretical study and photophysical characterization. All three emitters showed high electrochemical stability with reversible oxidation waves. MPA 2 -BTBTOx 4 was selected as the reference molecule for X-ray analysis, which revealed torsion angles of −59° and 86° between the donor (MPA) and acceptor (BTBTOx 4 ) units supporting their appropriate structural configuration to have TADF properties. Photophysical studies highlighted a noteworthy increase in PL efficiency upon deoxygenation for all three compounds. The oxygen-induced quenching of delayed fluorescence and time-resolved photoluminescence studies supported the presence of the TADF properties, further corroborated for PTz 2 -BTBTOx 4 and MPA 2 -BTBTOx 4 by DFT studies. Preliminary steady-state photophysical studies were also carried out on neat films of all three emitters, revealing a pronounced self-quenching of photoluminescence for PTz 2 -BTBTOx 4 and MPA 2 -BTBTOx 4 and a minimal self-quenching for POCz 2 -BTBTOx 4 , which maintains a high Φ PL (22%) comparable to that in Zeonex and half of that in PMMA. As a proof of concept, the three emitting molecules were tested as neat films in simple-structure OLED devices. In accordance with the photoluminescence data, POCz 2 -BTBTOx 4 , thanks to its sterically bulky structure, retains a good emission capacity even in a neat film and was also selected as an active matrix to build OLED devices by using two different deposition techniques: inkjet-printing and spin coating. 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source Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list)
subjects Benzothiophene
Coupling (molecular)
Cross coupling
Crystallography
Deoxygenation
Electrical measurement
Electrical properties
Electrochemical analysis
Electronic structure
Electrons
Emitters
Fluorescence
Inkjet printing
Organic chemistry
Oxidation
Photoluminescence
Quenching
Spin coating
Structural analysis
X ray analysis
title New [1]benzothieno[3,2-]benzothiophene-tetraoxide-based TADF emitters with a D-A-D structure for OLED applications
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