Polymer, coating composition comprising same, and organic light emitting element using same
A polymer, mole fraction technology, applied in the direction of luminescent materials, electrical components, coatings, etc., can solve the problem of solution concentration gradient change, defective devices, materials cannot be dissolved well, etc., to reduce the driving voltage, improve the use of Effects of lifetime characteristics, excellent thermal and optical stability
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preparation example 1
[0317]
[0318] (1) Preparation of Intermediate 5
[0319]
[0320] After dissolving 3-bromo-9-phenyl-9H-carbazole (9g, 27.9mmol) and 4-formylphenylboronic acid (4.18g, 27.9mmol) in anhydrous tetrahydrofuran (THF, 100mL), to it Put in Pd(PPh 3 ) 4 (0.32g, 0.28mmol) and 70ml2M potassium carbonate aqueous solution (K 2 CO 3 / H 2 0), the resulting mixture was refluxed for 6 hours. After cooling the reaction solution to room temperature, the organic layer was extracted. The reaction solution was concentrated and recrystallized with ethanol (EtOH) to obtain Intermediate 3 (8.9 g, yield 92%). MS:[M+H] + =348
[0321] Intermediate 3 (8.2 g, 23.6 mmol) was dissolved in dimethylformaldehyde (200 mL), N-bromosuccinimide (4.15 g, 23.6 mmol) was added thereto, and the resulting mixture was stirred at room temperature for 5 Hour. After distilled water was poured into the reaction solution to terminate the reaction, the organic layer was extracted. The reaction solution was ...
preparation example 2
[0326]
[0327] (1) Preparation of compound A1
[0328]
[0329] After intermediate 5 (3.65g, 8.615mmol), 4-(diphenylamino)phenylboronic acid (2.99g, 10.338mmol), Pd(PPh 3 ) 4 (498mg, 0.431mmol) and K 2 CO 3 (3.57g, 25.845mmol) was dissolved in anhydrous tetrahydrofuran (200ml) and distilled water (100ml), and the resulting solution was stirred at 70°C for 15 hours. The organic layer was extracted by using ethyl acetate and water. By using MgSO 4 After removing moisture from the organic layer, the solvent was removed under reduced pressure. The obtained material was subjected to column chromatography using ethyl acetate and hexane to separate and purify Compound A1. MS:[M+H] + =589
[0330] (2) Preparation of Compound A2
[0331]
[0332] Compound A2 was prepared in the same manner as in the method for preparing Compound A1 except that 4-(biphenylyl-4-ylamino)phenylboronic acid was used instead of 4-(diphenylamino)phenylboronic acid. MS:[M+H] + =741
[0333...
preparation example 3
[0354]
[0355] (1) Preparation of Compound B2
[0356]
[0357] (4-formylphenyl)boronic acid (4.91g, 32.778mmol), 3-bromobicyclo[4.2.0]oct-1(6),2,4-triene (5g, 27.315mmol), Pd( PPh 3 ) 4 (1.58g, 1.366mmol) and K 2 CO 3 (11.32g, 81.945mmol) was dissolved in anhydrous tetrahydrofuran (200ml) and distilled water (100ml), and the resulting solution was stirred at 70°C for 15 hours. The organic layer was extracted by using ethyl acetate and water. By using MgSO 4 After removing moisture from the organic layer, the solvent was removed under reduced pressure. The obtained material was subjected to column chromatography using ethyl acetate and hexane to isolate and purify Intermediate 7. MS:[M+H] + =209
[0358] Bromide methyl triphenyl Salt (13.41 g, 37.532 mmol) and potassium tert-butoxide (4.21 g, 37.532 mmol) were put into anhydrous tetrahydrofuran (30 ml), and the resulting solution was stirred. Thereafter, Intermediate 7 (3.90 g, 18.766 mmol) dissolved in anhyd...
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