Aromatic amine derivative containing benzophenone group and preparation method and application thereof
A technology of aromatic amines and benzophenone, which is applied in the field of aromatic amine derivatives and their preparation, can solve the problems of low luminous intensity, efficiency roll-off, and low external quantum efficiency of phosphorescent OLEDs, etc., and achieve good hole transport ability, low cost, and the effect of improving external quantum efficiency
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Embodiment 1
[0060] An aromatic amine derivative containing a benzophenone group has a molecular structure as shown in formula (I), named pBZ-DPA:
[0061]
[0062] The preparation method of the above-mentioned aromatic amine derivatives containing benzophenone group comprises the following steps:
[0063] S1. Preparation of (4-bromophenyl)(3-phenylimidazo[1,2-a]pyridin-2-yl)methanone:
[0064] Weigh (E)-1-(4-bromophenyl)-3-phenylprop-2-en-1-one 2.87g, 2-aminopyridine 0.94g, iodine 2.53g, 0.154g and 20mL chloroform in In a two-necked flask, a Michael ring closure reaction was carried out at a temperature of 75°C to obtain (4-bromophenyl)(3-phenylimidazo[1,2-a]pyridin-2-yl)methanone after treatment;
[0065] Its reaction equation is:
[0066]
[0067] S2. the preparation of formula (I) compound:
[0068] Weigh (4-bromophenyl)(3-phenylimidazo[1,2-a]pyridin-2-yl)methanone 188mg, diphenylamine 101mg, sodium tert-butoxide 72mg, tri-tert-butylphosphine 30mg, [1,3-bis(2,6-diisopropylphe...
Embodiment 2
[0072] An aromatic amine derivative containing a benzophenone group has a molecular structure as shown in formula (II), named pBZ-TPA:
[0073]
[0074] The preparation method of the above-mentioned aromatic amine derivatives containing benzophenone group comprises the following steps:
[0075] S1. The preparation of (4-bromophenyl)(3-phenylimidazo[1,2-a]pyridin-2-yl)methanone is the same as in Example 1;
[0076] S2. the preparation of formula (Ⅱ) compound:
[0077] Weigh (4-bromophenyl)(3-phenylimidazo[1,2-a]pyridin-2-yl)methanone 188mg, 4-triphenylamine borate 235mg, 2mol / L sodium carbonate aqueous solution 3ml, four (Triphenylphosphine)palladium 40mg and 5mL of toluene were placed in a reaction tube, heated, stirred and refluxed for 12 hours under the protection of nitrogen at 120°C. After the reaction, the crude product was cooled, distilled, extracted, dried, concentrated, and separated; collected by cooling A yellow turbid liquid was obtained, the turbid liquid was...
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