N-type compound containing naphthyl[1,2]imidazole as well as preparation and application thereof
A technology of imidazole and compound is applied in the field of electroluminescent materials to achieve the effects of promoting equilibrium, determining molecular weight and single molecular structure
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Embodiment 1
[0029] The preparation of a kind of n-type compound 1 containing naphtho[1,2]imidazole of the present embodiment, the reaction formula is as follows:
[0030]
[0031] The specific preparation steps are: in a 250 ml single-necked flask, N'-benzene-1,2-diaminonaphthalene (12mmol, 2.8g) and terephthaloyl chloride (1.02g, 5mmol) were added to 100mL of dichloromethane Dissolved in , then added 2 ml of triethylamine, and reacted at room temperature for 10 hours. Then the solid precipitated in the reaction was filtered off, and rinsed with a small amount of ethanol and acetone successively. After the obtained white solid was dried, it was added into a 100 mL one-necked flask, mixed with 50 mL of acetic acid and heated to 110° C. for 12 hours. The mixture was then poured into 250 mL of water, and the product was extracted with dichloromethane. The organic phase was dried over anhydrous magnesium sulfate, and the solvent was removed after separation. The white solid was separated...
Embodiment 2
[0033] The preparation of a kind of n-type compound 2 containing naphtho[1,2]imidazole of the present embodiment, the reaction formula is as follows:
[0034]
[0035] The specific preparation steps are: in a 250 ml single-necked flask, N-benzene-1,2-diaminonaphthalene (12mmol, 2.8g) and terephthaloyl chloride (1.02g, 5mmol) were added to 100mL of dichloromethane Dissolved, then added 2 ml of triethylamine, and reacted at room temperature for 10 hours. Then the solid precipitated in the reaction was filtered off, and rinsed with a small amount of ethanol and acetone successively. After the obtained white solid was dried, it was added into a 100 mL one-necked flask, mixed with 50 mL of acetic acid and heated to 110° C. for 12 hours. The mixture was then poured into 250 mL of water, and the product was extracted with dichloromethane. The organic phase was dried over anhydrous magnesium sulfate, and the solvent was removed after separation. The white solid was separated and ...
Embodiment 3
[0037] The preparation of a kind of n-type compound 3 containing naphtho[1,2]imidazole of the present embodiment, the reaction formula is as follows:
[0038]
[0039] The specific preparation steps are: in a 250 ml single-necked flask, N'-benzene-1,2-diaminonaphthalene (12mmol, 2.8g) and 1,3,5-benzenetricarboxylic acid chloride (0.8g, 3mmol) were added to Dissolve in 100 mL of dichloromethane, then add 2 mL of triethylamine, and react at room temperature for 10 hours. Then the solid precipitated in the reaction was filtered off, and rinsed with a small amount of ethanol and acetone successively. After the obtained white solid was dried, it was added into a 100 mL one-necked flask, mixed with 50 mL of acetic acid and heated to 110° C. for 12 hours. The mixture was then poured into 250 mL of water, and the product was extracted with dichloromethane. The organic phase was dried over anhydrous magnesium sulfate, and the solvent was removed after separation. The white solid was...
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