Methoxytriphenylamine-fluorene-containing copolymer, and preparation method and application thereof
A technology containing methoxytriphenylamine and methoxytriphenylamine is applied in the fields of methoxytriphenylamine-fluorene copolymer, preparation and application thereof, and can solve the problems of low optical and thermal stability, poor solubility, and blue light of materials. Insufficient saturation chromaticity and other problems, to achieve the effect of improving light and thermal stability, improving stability and high luminous efficiency
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specific Embodiment approach 1
[0028] Specific embodiment one: the number average molecular weight M of this embodiment containing methoxytriphenylamine-fluorene copolymer n =23000~56000, its structural formula is as follows:
[0029]
[0030] In this embodiment, the methoxy-containing triphenylamine-fluorene copolymer is poly[2,7-(9,9-dioctylfluorene)-alternating-N-phenyl-N-(4-methoxyphenyl)aniline ].
specific Embodiment approach 2
[0031] Specific embodiment two: the preparation method of the present embodiment containing methoxy triphenylamine-fluorene copolymer is realized according to the following steps:
[0032] 1. Add 4-methoxyaniline and 1-bromo-4-iodobenzene to the organic solvent a at a molar ratio of 1:(2~2.5), then add the palladium catalyst Pd 2 (dba) 3 , 1,1'-bis(diphenylphosphino)ferrocene (DPPF) and sodium tert-butoxide (t-BuONa), the reaction temperature is controlled at 90~105℃, the reaction is 5~10h, and then the organic Solvent a, the reaction product after rotary evaporation is separated by chromatographic column after extraction and distillation to obtain N,N-bis(4-bromophenyl)-4-(4-methoxy)aniline monomer (M );
[0033] 2. Mix 9,9-dioctylfluorene-2,7-diboronic acid cis(1,3-propanediol) ester and N,N-bis(4-bromophenyl) at a molar ratio of 1:(1~1.3) )-4-(4-methoxy)aniline monomer (M) is added in the organic solvent b, and then the palladium catalyst Pd(PPh 3 ) 4 and 2-3 mol / L sod...
specific Embodiment approach 3
[0038] Embodiment 3: This embodiment is different from Embodiment 2 in that the organic solvent a in step 1 is toluene, xylene, THF, dioxane, DMF or DMSO. Other steps and parameters are the same as in the second embodiment.
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