Fluorene-containing organic compound and application thereof on OLED (organic light emitting diode) device
A technology of organic compounds and compounds, applied in the fields of organic chemistry, electro-solid devices, electrical components, etc., can solve different problems and so on
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Embodiment 1
[0083] Example 1: Synthesis of intermediate A1:
[0084] synthetic route:
[0085]
[0086] In a 250ml four-neck flask, add 11.8g 1,4-dibromobenzene (0.05mol), 1.2gMg powder (0.05mol), 60ml tetrahydrofuran, and reflux for 4 hours under a nitrogen atmosphere. The reaction is complete. Reagent
[0087] 9.0g of 9-fluorenone (0.05mol) was dissolved in 50mL of tetrahydrofuran, and the above reagent was added dropwise, and reacted at 60℃ for 24 hours, a large amount of white salt was formed, and saturated NHCl was added. 4 Solution until the precipitation disappears, the formal salt is converted into tertiary alcohol; after the reaction is completed, it is extracted with 100ml ether, the extract is dried with anhydrous sodium sulfate, the solution is evaporated to remove the solvent until there is no distillate, and the tertiary alcohol crude product is obtained. The mixed solvent of petroleum ether and dichloromethane (volume ratio 3:2) was used as the eluent to be purified by neutral si...
Embodiment 2
[0089] Example 2: Synthesis of Intermediate A2:
[0090] synthetic route:
[0091]
[0092] The intermediate A2 was prepared according to the synthesis method of the intermediate A1 in Example 1, except that 1,1'-biphenyl was used instead of the compound bromobenzene;
[0093] Use DEI-MS to identify the compound, molecular formula C 31 H 21 Br, detection value [M+1] + =473.31, the calculated value is 472.08.
Embodiment 3
[0094] Example 3: Synthesis of Intermediate A3:
[0095] synthetic route:
[0096]
[0097] Intermediate A3 was prepared according to the synthesis method of intermediate A1 in Example 1, except that benzene was used instead of bromobenzene in the third step of the reaction;
[0098] Use DEI-MS to identify the compound, molecular formula C 25 H 17 Br, detection value [M+1] + =397.21, calculated value 396.05.
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