Bis(trimethylsilyl)phenyl-bridged D-A molecules: Synthesis, spectroscopic properties and for achieving deep-blue emitting materials. (March 2020)
- Record Type:
- Journal Article
- Title:
- Bis(trimethylsilyl)phenyl-bridged D-A molecules: Synthesis, spectroscopic properties and for achieving deep-blue emitting materials. (March 2020)
- Main Title:
- Bis(trimethylsilyl)phenyl-bridged D-A molecules: Synthesis, spectroscopic properties and for achieving deep-blue emitting materials
- Authors:
- Shen, Ziqiu
Zhu, Xiangyu
Tang, Weiguo
Zheng, Yu
Zhou, Zhikuan
Feng, Xin Jiang
Zhao, Zujin
Lu, Hua - Abstract:
- Abstract: Usually, donor (D)-acceptor (A) π -conjugated molecules display weak fluorescence with a long wavelength due to effective intramolecular charge transfer. In this paper, a series of donor- π -acceptor (D- π -A) molecules, incorporated with bis(trimethylsilyl)phenyl as a bridging group to twist molecular structure, were synthesized by Suzuki cross-coupling using diphenylamino and oxadiazole/triazole as electron-donating group and electron-withdrawing group, respectively. The resulting molecules exhibited high thermal stabilities and strong fluorescence at deep-blue regions in the solid state. Aggregation-induced emission enhancement (AIEE) of p -DSiTO was observed because of the suppression of molecular vibration and rotation in the aggregated state. Furthermore, the locally excited (LE) emission was significantly increased to show hybridized local and charge-transfer (HLCT) emission in the aggregated state. Theoretical calculations and electrochemical measurements were carried out for understanding optical and electrochemical properties in these molecules. Non-doped organic light-emitting diodes (OLEDs) fabricated using p -DSiTO as emitter showed deep-blue emission with CIEx, y (Commission Internationale de l'Eclairage) of (0.160, 0.105). Graphical abstract: Image 1 Highlights: D- π -A molecules with bis(trimethylsilyl)phenyl bridge were synthesized. The resulting molecules exhibited strong deep-blue emission. TD-DFT calculations and electrochemical measurementsAbstract: Usually, donor (D)-acceptor (A) π -conjugated molecules display weak fluorescence with a long wavelength due to effective intramolecular charge transfer. In this paper, a series of donor- π -acceptor (D- π -A) molecules, incorporated with bis(trimethylsilyl)phenyl as a bridging group to twist molecular structure, were synthesized by Suzuki cross-coupling using diphenylamino and oxadiazole/triazole as electron-donating group and electron-withdrawing group, respectively. The resulting molecules exhibited high thermal stabilities and strong fluorescence at deep-blue regions in the solid state. Aggregation-induced emission enhancement (AIEE) of p -DSiTO was observed because of the suppression of molecular vibration and rotation in the aggregated state. Furthermore, the locally excited (LE) emission was significantly increased to show hybridized local and charge-transfer (HLCT) emission in the aggregated state. Theoretical calculations and electrochemical measurements were carried out for understanding optical and electrochemical properties in these molecules. Non-doped organic light-emitting diodes (OLEDs) fabricated using p -DSiTO as emitter showed deep-blue emission with CIEx, y (Commission Internationale de l'Eclairage) of (0.160, 0.105). Graphical abstract: Image 1 Highlights: D- π -A molecules with bis(trimethylsilyl)phenyl bridge were synthesized. The resulting molecules exhibited strong deep-blue emission. TD-DFT calculations and electrochemical measurements were carried out. Non-doped organic light-emitting diode was fabricated using p -DSiTO as an emitter. … (more)
- Is Part Of:
- Dyes and pigments. Volume 174(2020)
- Journal:
- Dyes and pigments
- Issue:
- Volume 174(2020)
- Issue Display:
- Volume 174, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 174
- Issue:
- 2020
- Issue Sort Value:
- 2020-0174-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-03
- Subjects:
- D-A molecules -- Spectroscopy -- TICT -- Deep-blue emitter -- Solid emission
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2019.108063 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12513.xml