Organic light-emitting element with low operating voltage and High efficiency
A technology of organic light-emitting elements and light-emitting layers, which is applied in electrical components, light-emitting materials, and electric solid-state devices to achieve high-efficiency effects.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Synthetic example 1
[0130]Synthesis Example 1: Synthesis of [Chemical Formula 1]
[0131] [Reaction Formula 1-1] Synthesis of [Intermediate 1-a]
[0132]
[0133] Bromobenzene (8.0g, 0.050mol), 2,6-dimethylaniline (6.2g, 0.050mol), palladium acetate (0.22g, 1mmol), 2,2'-bis(biphenylphosphino)-1 - 1'-binaphthalene (1.3g, 2mmol) and sodium tert-butanol (12.2g, 0.120mol) were put into 100ml of toluene, and the flow was changed for 12 hours. After cooling to room temperature, it extracted with ethyl acetate and separated by column chromatography to obtain 7.3 g of [Intermediate 1-a] (yield 73%).
[0134] [Reaction Formula 1-2] Synthesis of [Chemical Formula 1]
[0135]
[0136] 1,6-Dibromopyrene (4g, 0.011mol), [Intermediate 1-a] (5.0g, 0.025mol) synthesized in the [Reaction Formula 1-1], sodium tert-butanol (5.3g, 0.055mol), palladium acetate (0.1g, 0.44mmol), and tri-tert-butylphosphine (0.36g, 1.7mmol) were put into 50mL of toluene, and the flow was changed for 12 hours. After cooling to...
Synthetic example 2
[0137] Synthesis Example 2: Synthesis of [Chemical Formula 2]
[0138] [Reaction Formula 2-1] Synthesis of [Intermediate 2-a]
[0139]
[0140]
[0141] In the [reaction formula 1-1], use 2,6-diethylaniline instead of 2,6-dimethylaniline, and use the same method to obtain [intermediate 2-a] (yield 75 %).
[0142] [Reaction Formula 2-2] Synthesis of [Chemical Formula 2]
[0143]
[0144] In said [reaction formula 1-2], use [intermediate 2-1] synthesized in [reaction formula 2-1] instead of intermediate [1-a], and use the same method to obtain [chemical formula 2 ] (yield 63%).
Synthetic example 3
[0145] Synthesis Example 3: Synthesis of [Chemical Formula 3]
[0146] [Reaction Formula 3-1] Synthesis of [Intermediate 3-a]
[0147]
[0148] In the [reaction formula 1-1], use 2,6-diphenylamine isopropyl ester instead of 2,6-dimethylaniline and use the same method to obtain [intermediate 3-a] (yield 75%).
[0149] [Reaction Formula 3-2] Synthesis of [Chemical Formula 3]
[0150]
[0151] In the [reaction formula 1-2], use the [intermediate 3-a] synthesized in the [reaction formula 3-1] instead of [intermediate 1-a], and obtain [ Chemical formula 3] (yield 56%).
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 