Hyperbranched electrophosphorescent conjugated polymer with metal complex as core and its use
A technology of conjugated polymers and metal complexes, applied in the field of hyperbranched electrophosphorescent conjugated polymers, can solve the problems of low electroluminescence efficiency, and achieve the effect of simple synthesis method and high application value
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Embodiment 1
[0040] The synthetic reference patent of 2-(3'-bromo-phenyl)-pyridine [Paul F. Ranken, Baton La. Rouge,, U.S. Patent 4,554,352].
[0041] Add 2-phenylpyridine (1 mole), anhydrous aluminum trichloride (1.2 mole), nitrobenzene (4.9 mole) in the 500ml there-necked flask with constant pressure funnel, thermometer, under nitrogen protection, be heated to 85-95°C. Liquid bromine (1.2 moles) was slowly dropped into the mixed solution and reacted at 85-95°C for 12 hours. The reaction mixture was poured into crushed ice. After the bromine was washed away, the product was purified by column chromatography to obtain a white needle-like solid.
[0042]
Embodiment 2
[0044] The synthesis of 5-bromo-2-phenylpyridine refers to [Lamansky, S.; Djurovich, P.; Murphy, D.; Abdel-Razzaq, F.; Kwong, R.; Tsyba, I.; Bortz, M.; Methods reported by Mui, B.; Bau, R.; Thompson, M.E.; Inorganic Chemistry. 2001, 40, 1704-1711]
[0045] Weigh 6.48 g of anhydrous zinc chloride, 0.49 g of tetrakis(triphenylphosphine) palladium, and 5.5 g of 2,5-dibromopyridine in a glove box, and inject 25, 25, and 35 ml of THF into solutions respectively.
[0046]31.3 ml of BuLi and 20 ml of THF were added to a 500 ml three-necked flask equipped with a constant pressure funnel and a thermometer. After liquid nitrogen was cooled to -78°C, a solution containing bromobenzene 5ml / THF (25ml) was added dropwise, and the reaction was continued at -70°C for 40min. Then the zinc chloride / THF solution was added dropwise from the constant pressure funnel at -70°C. After gradually raising the temperature to room temperature, the reaction was carried out for 30 minutes. Tetrakis(triph...
Embodiment 3
[0049] The synthetic reaction steps of 5-bromo-2-(4'-methylphenyl)-pyridine are as in Example 2
[0050] The bromobenzene in the raw material is changed into p-bromotoluene, finally obtains 3.58 grams of light yellow powder,
[0051] The yield was 60.8%. 1 HNMR and GC-MASS tests showed that it was the target product.
[0052]
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