Triarylamine-based compound and preparation method thereof, and applications of triarylamine-based compound in organic electroluminescent devices
An electroluminescent device, triarylamine technology, applied in the fields of electro-solid devices, chemical instruments and methods, electrical components, etc., can solve problems such as different problems, reduce cross-color phenomenon, good film-forming properties, and good industrialization prospects Effect
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Embodiment 1 3
[0046] The preparation of embodiment 1 triaromatic amine compound
Embodiment 1-1
[0047] Embodiment 1-1: Preparation of compound 1
[0048] The chemical reaction equation that takes place in the preparation process of compound 1 is as follows:
[0049]
[0050] Concrete preparation steps are as follows:
[0051] (1) Preparation of Intermediate 1
[0052] 10mmol 4-(1-naphthyl)aniline (2.2g), 10mmol 1-bromopyrene (2.8g), 20mmol sodium tert-butoxide (2.0g), 0.1mmol Pd 2 (dba) 3 (0.1g) and 50ml of toluene were added to the reaction flask in turn, refluxed for 10h under nitrogen protection, cooled to room temperature, added 100ml of water, separated, the aqueous layer was extracted with ethyl acetate and combined with the organic layer, and saturated saline and water were sequentially After washing, the organic layer was dried with magnesium sulfate, filtered, the filtrate was rotary evaporated, and passed through a silica gel column to obtain Intermediate 1 with a HPLC purity of 99.5%;
[0053] (2) Preparation of compound 1
[0054] 10mmol of the above ...
Embodiment 1-2
[0055] Embodiment 1-2: Preparation of Compound 2
[0056] The chemical reaction equation that takes place in the preparation process of compound 2 is as follows:
[0057]
[0058] Concrete preparation steps are as follows:
[0059] (1) Preparation of Intermediate 2
[0060] 10mmol 4-(2-naphthyl)aniline (2.2g), 10mmol 1-bromopyrene (2.8g), 20mmol sodium tert-butoxide (2.0g), 0.1mmol Pd 2 (dba) 3 (0.1g) and 50ml of toluene were added to the reaction flask in turn, refluxed for 10h under nitrogen protection, cooled to room temperature, added 100ml of water, separated, the aqueous layer was extracted with ethyl acetate and combined with the organic layer, and saturated saline and water were sequentially After washing, the organic layer was dried with magnesium sulfate, filtered, the filtrate was rotary evaporated, and passed through a silica gel column to obtain intermediate 2 with a HPLC purity of 99.4%;
[0061] (2) Preparation of Compound 2
[0062] 10mmol of the above ...
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