Feasible structure-modification strategy for inhibiting aggregation-caused quenching effect and constructing exciton conversion channels in acridone-based emitters. Issue 19 (29th April 2019)
- Record Type:
- Journal Article
- Title:
- Feasible structure-modification strategy for inhibiting aggregation-caused quenching effect and constructing exciton conversion channels in acridone-based emitters. Issue 19 (29th April 2019)
- Main Title:
- Feasible structure-modification strategy for inhibiting aggregation-caused quenching effect and constructing exciton conversion channels in acridone-based emitters
- Authors:
- Wan, Qing
Zhang, Bing
Tong, Jialin
Li, Yin
Wu, Haozhong
Zhang, Han
Wang, Zhiming
Pan, Yuyu
Tang, Ben Zhong - Abstract:
- Abstract : The introduction of multiple rotors donors and benzonitrile group in ADOs would increases effectively OLED emitters' performance by inhibiting aggregation-caused quenching effect and constructing exciton conversion channels. Abstract : Acridone (ADO) is an anthracene-based derivative that plays an important role in the construction of organic light-emitting diode emitters. However, ADO suffers from an aggregation-caused quenching (ACQ) effect because of its strong intermolecular stacking and tendency to form excimers. In this work, we appended some electron-donating moieties with different rotors and substitution patterns on ADO to prepare six ADO-based derivatives. In addition, a benzonitrile group was introduced onto the nitrogen atom of the ADO unit to fabricate a high-energy charge-transfer (CT) state that formed a reverse intersystem crossing (RISC) channel. Systematic spectral measurements revealed that the rotors effectively suppressed the ACQ effect. In addition, aggregation-enhanced emission (AEE) was observed for the ADO derivatives modified with triphenylamine (TPA) because of the existence of multiple rotors and propeller-like conformation in TPA block. Theoretical calculations and the performance of electroluminescent devices containing the derivatives confirmed that the exciton conversion channel was constructed at the high-energy level and activated during device operation. Although the performance of these ADO-based derivatives was not ideal inAbstract : The introduction of multiple rotors donors and benzonitrile group in ADOs would increases effectively OLED emitters' performance by inhibiting aggregation-caused quenching effect and constructing exciton conversion channels. Abstract : Acridone (ADO) is an anthracene-based derivative that plays an important role in the construction of organic light-emitting diode emitters. However, ADO suffers from an aggregation-caused quenching (ACQ) effect because of its strong intermolecular stacking and tendency to form excimers. In this work, we appended some electron-donating moieties with different rotors and substitution patterns on ADO to prepare six ADO-based derivatives. In addition, a benzonitrile group was introduced onto the nitrogen atom of the ADO unit to fabricate a high-energy charge-transfer (CT) state that formed a reverse intersystem crossing (RISC) channel. Systematic spectral measurements revealed that the rotors effectively suppressed the ACQ effect. In addition, aggregation-enhanced emission (AEE) was observed for the ADO derivatives modified with triphenylamine (TPA) because of the existence of multiple rotors and propeller-like conformation in TPA block. Theoretical calculations and the performance of electroluminescent devices containing the derivatives confirmed that the exciton conversion channel was constructed at the high-energy level and activated during device operation. Although the performance of these ADO-based derivatives was not ideal in terms of efficiency, the results confirmed the feasibility of this structure modification strategy to simultaneously inhibit the ACQ effect and construct excitons conversion channels. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 21:Issue 19(2019)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 21:Issue 19(2019)
- Issue Display:
- Volume 21, Issue 19 (2019)
- Year:
- 2019
- Volume:
- 21
- Issue:
- 19
- Issue Sort Value:
- 2019-0021-0019-0000
- Page Start:
- 9837
- Page End:
- 9844
- Publication Date:
- 2019-04-29
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9cp01706b ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 10401.xml