[7] helicene organic light-emitting material based on triaryl borane and application of [7] helicene organic light-emitting material in sign reversal of induced circular polarization light emission
A technology of triarylborane and luminescent materials, which is applied in the field of sign inversion of circularly polarized luminescence, can solve problems such as 7B-HC structural instability, increase the asymmetry factor of luminescence, have universal applicability, and be easy to scale production Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0034] The present invention also provides a method for preparing a triarylborane-based [7]helicene organic luminescent material, comprising:
[0035] Halide precursors are used as raw materials to carry out borylation reaction to obtain.
[0036] In some embodiments, the halide precursor is a bromide / iodide precursor.
[0037] In some embodiments, the bromide precursor is 9-bromo[7]helicene; the bromide precursor 9-bromo[7]helicene (9Br-[7]HC) is obtained through benzyl(dibromo) Methane coupling reactions were obtained according to published procedures.
[0038] In some embodiments, the iodide precursor is 9-(2-iodophenyl)[7]helicene. 9B(OH) 2 The Suzuki coupling reaction of -[7]HC with o-diiodobenzene proceeds very smoothly, providing the iodide precursor 9-(2-iodophenyl)[7]helicene (9I Ph-[7] HC).
[0039] In some embodiments, the borylation reaction includes: lithiation of n-butyllithium and quenching of micyl borofluoride. [7]helicenes based on triarylboranes are al...
Embodiment 1
[0043] 9-Micylboron[7]helicene (9B-[7]HC):
[0044] To a solution of 9-bromo[7]helicene (9Br-[7]HC) (700 mg, 1.53 mmol) in anhydrous THF (40 mL) was slowly added dropwise n-butyllithium (1.2 mL, 1.6M, 1.84mmol) in n-hexane. The mixture was stirred at the same temperature for 1 hour. A solution of micyl borofluoride (1.23 g, 4.59 mmol) in anhydrous THF (10 mL) was added via syringe. The reaction mixture was slowly warmed to room temperature and stirred overnight. with saturated NH 4 The reaction was quenched with Cl solution, and the organic phase was washed with CH 2 Cl 2 extraction. The combined organic layers were washed with anhydrous Na 2 SO 4 Dry, filter, and concentrate under reduced pressure. The resulting residue was subjected to silica gel column chromatography (20 / 1 petroleum ether / CH 2 Cl 2 , R f =0.38) purification afforded 508 mg (0.81 mmol) of 9B-[7]HC as a yellow solid in 53% yield: mp 318.0°–319.0°C; [α] 25 (P)-isomer is +680.8, (M)-isomer is –700....
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com