Organic light emitting device
A technology of organic light-emitting devices and organic substances, which is applied in the fields of electrical solid-state devices, semiconductor devices, semiconductor/solid-state device manufacturing, etc., and can solve problems such as shortened lifespan, single types of light extraction materials, and unsatisfactory effects
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[0127] The preparation of the cover layer can be any one of vacuum evaporation method, spin coating method, vapor deposition, blade coating method, laser thermal transfer printing, electrospray coating method, slit coating method and dip coating method. In the present invention, the method of vacuum evaporation is preferably used.
[0128] The organic light-emitting device of the present invention can be widely used in the fields of panel display, lighting source, flexible OLED, electronic paper, organic photoreceptor or organic thin film transistor, signboard, signal lamp and the like.
Embodiment 1
[0131] [Example 1] Synthesis of Compound 1-1
[0132]
[0133] Step1: add benzidine-compound f (1.35g, 8mmol), compound g (1.55g, 6.67mmol), Pd in the reactor 2 (dba) 3 (0.17g, 0.2mmol), P(t-Bu) 3 (0.14, 0.67mmol), NaOt-Bu (2.24g, 20mmol), 100mL toluene solution, reacted at 100°C for 24h, extracted the organic phase with ether and water after the reaction, and used MgSO 4 After drying, the organic matter was concentrated, subjected to column chromatography, and recrystallized to obtain intermediate 1-b (1.61 g, 75%).
[0134] Step2: Add compound a (1.53g, 8mmol), (3.15g, 17.5mmol) of N-bromosuccinimide and (0.5g, 2.7mmol) of p-toluenesulfonic acid in the reactor and dissolve them in 30ml of acetonitrile , and stirred at 50°C for about 12 hours. Cool to room temperature, depressurize, filter to collect crystals, and then wash with methanol to obtain compound b. Take compound b (1.80g, 6.67mmol) and methyl bromide c (0.76g, 8mmol), add potassium tert-butoxide (2.83g, 2...
Embodiment 2
[0139] [Example 2] Synthesis of Compound 1-3
[0140] Compound 1-3 (3.86 g, 62%) was obtained according to the synthesis method of compound 1-1.
[0141] Mass Spectrum m / z: 741.32 (calculated: 741.31). Theoretical element content (%)C 55 h 39 N 3 : C, 89.04; H, 5.30; N, 5.68 Measured element content (%): C, 89.05; H, 5.30; N, 5.67. The above results confirmed that the obtained product was the target product.
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