Benzo[4, 5]thieno-S, S-dioxide-[3, 2-b]benzofurans: synthesis, properties and application in electroluminescent devices. Issue 26 (8th June 2020)
- Record Type:
- Journal Article
- Title:
- Benzo[4, 5]thieno-S, S-dioxide-[3, 2-b]benzofurans: synthesis, properties and application in electroluminescent devices. Issue 26 (8th June 2020)
- Main Title:
- Benzo[4, 5]thieno-S, S-dioxide-[3, 2-b]benzofurans: synthesis, properties and application in electroluminescent devices
- Authors:
- Ma, Weimin
Liu, Guanhao
Zhou, Lu
Li, Baolin
Wang, Ying - Abstract:
- Abstract : Four organic light-emitting diodes based on the first mixed thieno- S, S -dioxide-furan acenes (BTOBFs) exhibit blue to green tunable luminescence, and respectable EQE of up to 6.49% has been achieved. Abstract : The first mixed thieno- S, S -dioxide-furan acenes (BTOBFs) were constructed by simple oxidation of benzo[4, 5]thieno-[3, 2- b ]benzofurans (BTBFs). After oxidation, the absorption and emission peaks of the compounds undergo a significant red shift, and fluorescence quantum yields ( Φ f = 0.23–0.90) are increased several to several tens of times thanks to the more rigid and more π-extended molecular backbone as well as significant intramolecular charge transfer. F-BTOBF and F, Cl-BTOBF displayed somewhat low device performance with external quantum efficiency (EQE) of 0.72–0.78% yet desirable blue emission. However, when we introduce strong electron-donating groups such as carbazolyl or triphenylamino group into BTOBFs to further tune the electronic properties, the resulting compounds 2-NPhCz-BTOBF and 2-TPA-BTOBF exhibit not only much red shift in absorption and fluorescence, but also significant improvement in hole mobility. As a result, these two compounds displayed much better device performance with respectable EQEs of 5.82–6.49%, low turn-on voltage less than 3 V and lower efficiency roll-off. Therefore, for the first time, this work reports the huge potential of mixed thieno- S, S -dioxide-furan acenes as blue to green emitters for high-performanceAbstract : Four organic light-emitting diodes based on the first mixed thieno- S, S -dioxide-furan acenes (BTOBFs) exhibit blue to green tunable luminescence, and respectable EQE of up to 6.49% has been achieved. Abstract : The first mixed thieno- S, S -dioxide-furan acenes (BTOBFs) were constructed by simple oxidation of benzo[4, 5]thieno-[3, 2- b ]benzofurans (BTBFs). After oxidation, the absorption and emission peaks of the compounds undergo a significant red shift, and fluorescence quantum yields ( Φ f = 0.23–0.90) are increased several to several tens of times thanks to the more rigid and more π-extended molecular backbone as well as significant intramolecular charge transfer. F-BTOBF and F, Cl-BTOBF displayed somewhat low device performance with external quantum efficiency (EQE) of 0.72–0.78% yet desirable blue emission. However, when we introduce strong electron-donating groups such as carbazolyl or triphenylamino group into BTOBFs to further tune the electronic properties, the resulting compounds 2-NPhCz-BTOBF and 2-TPA-BTOBF exhibit not only much red shift in absorption and fluorescence, but also significant improvement in hole mobility. As a result, these two compounds displayed much better device performance with respectable EQEs of 5.82–6.49%, low turn-on voltage less than 3 V and lower efficiency roll-off. Therefore, for the first time, this work reports the huge potential of mixed thieno- S, S -dioxide-furan acenes as blue to green emitters for high-performance OLEDs. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 8:Issue 26(2020)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 8:Issue 26(2020)
- Issue Display:
- Volume 8, Issue 26 (2020)
- Year:
- 2020
- Volume:
- 8
- Issue:
- 26
- Issue Sort Value:
- 2020-0008-0026-0000
- Page Start:
- 8796
- Page End:
- 8803
- Publication Date:
- 2020-06-08
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Optical materials -- Research -- Periodicals
Electronics -- Materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tc# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9tc06790f ↗
- Languages:
- English
- ISSNs:
- 2050-7526
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13810.xml