A kind of phosphorescent platinum complex as oled doping material and its application
A technology of platinum complexes and doping materials, applied in the field of phosphorescent platinum complexes, can solve problems such as unsatisfactory lifetime performance, and achieve the effects of good industrialization prospects, improved luminous efficiency, and high luminous efficiency
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[0054] The specific reaction types involved in the preparation of the compounds of the present invention are classified as follows:
[0055] Reaction condition 1:
[0056] In a 250mL three-neck flask, under nitrogen protection, 0.02mol reactant A, 0.022mol reactant B, 0.05mol sodium tert-butoxide, 0.2mmol Pd 2 (dba) 3 Add 0.2mmol tri-tert-butylphosphine into 150mL toluene, stir and mix, heat to 110-120°C, reflux for 12-16 hours, and the reaction is complete; naturally cool to room temperature, filter, and the filtrate is rotary evaporated under reduced pressure until there is no distillate. Neutral silica gel column to obtain the product.
[0057] Reaction condition 2:
[0058] Add 0.05mol of reactant C, 41.6g of N-bromosuccinimide (NBS), 500mL of dichloromethane and 500mL of acetonitrile into the three-necked flask in turn, stir at room temperature for 24h, after the reaction, the precipitated solid product is decompressed Suction filtration, the resulting solid product w...
preparation Embodiment 1
[0078]
[0079] Under a nitrogen atmosphere, weigh 0.01mol of reactant S-1 and dissolve it in 45mL of tetrahydrofuran, cool down to -78°C, slowly drop into a cyclohexane solution containing 0.02mol of n-butyllithium, after the dropwise addition, keep stirring for 30 minutes Slowly add a tetrahydrofuran solution containing 0.035mol trimethyl borate dropwise. After the dropwise addition, slowly warm up to room temperature and keep warm for 10 hours. After the reaction, cool down to 0°C and slowly drop in distilled water. Stir for 1 hour, then rise to room temperature; extract the reaction solution with 150 mL of ethyl acetate, wash the extract with 150 mL of saturated brine three times, and finally dry over anhydrous magnesium sulfate, and distill the solution under reduced pressure, and distill the obtained solid with 400 mL of V 甲苯 :V 乙醇 =3:1 mixed solution was recrystallized to obtain E-1.
[0080] In a 250mL three-neck flask, under nitrogen protection, 0.02mol reactant A...
preparation Embodiment 2
[0085]
[0086] Under a nitrogen atmosphere, weigh 0.01mol of reactant S-2 and dissolve it in 45mL of tetrahydrofuran, cool down to -78°C, slowly drop into a cyclohexane solution containing 0.02mol of n-butyllithium, after the dropwise addition, keep stirring for 30 minutes Slowly add a tetrahydrofuran solution containing 0.035mol trimethyl borate dropwise. After the dropwise addition, slowly warm up to room temperature and keep warm for 10 hours. After the reaction, cool down to 0°C and slowly drop in distilled water. Stir for 1 hour, then rise to room temperature; extract the reaction solution with 150 mL of ethyl acetate, wash the extract with 150 mL of saturated brine three times, and finally dry over anhydrous magnesium sulfate, and distill the solution under reduced pressure, and distill the obtained solid with 400 mL of V 甲苯 :V 乙醇 =3:1 mixed solution was recrystallized to obtain E-2.
[0087]In a 250mL three-neck flask, under nitrogen protection, 0.02mol reactant A-...
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