Preparation method and application of derivative by taking dibenzofuran as skeleton core
A derivative and diphenyl technology, applied in the field of derivative compounds, can solve problems such as the inability to produce high-performance light-emitting devices, and achieve the effects of increasing driving life, improving efficiency and life, and high luminous efficiency
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Embodiment 1
[0031] Embodiment 1: the synthesis of compound 001
[0032] Concrete synthetic route is as follows:
[0033]
[0034] Weigh 36.00g of 1,6-dibromopyrene, 104.21g of 14H-dibenzofurocarbazole, 13.46g of potassium tert-butoxide, 0.41g of palladium(II) acetate, 0.45g of tri-tert-butylphosphine, and use 250ml of toluene Dissolve and react at 80°C for 10 hours under nitrogen protection. The reaction solution was filtered, the obtained crude product was purified by silica gel chromatography, and the obtained solid was recrystallized from toluene and dried to obtain 74.11 g of light gray solid compound 1,6-bis(14H-dibenzofurocarbazole)pyrene , the yield is more than 83%, and the HPLC purity is greater than 98%. Mass spectrum: calculated value 892.95; found value 892.93. Elemental analysis: calculated value C: 86.08%; H: 3.61%; N: 3.14%; O: 7.17%; tested value C: 86.10%; H: 3.60%; N: 3.13%; O: 7.17%.
[0035]
Embodiment 2
[0036] Embodiment 2: the synthesis of compound 002
[0037] Concrete synthetic route is as follows:
[0038]
[0039] Weigh 35.20g of 2,7-dibromo-9,9-dimethylfluorene, 107.68g of 14H-dibenzofurocarbazole, 14.36g of potassium tert-butoxide, 0.48g of palladium(II) acetate, tri-tert-butyl 0.54 g of base phosphorus was dissolved in 250 ml of toluene, and reacted at 82° C. for 11 hours. The reaction solution was filtered, the obtained crude product was purified by silica gel chromatography, the obtained solid was recrystallized from toluene, and dried to obtain 75.22 g of light gray solid compound 14,14'-(9,9-dimethylfluorenediyl)bis (14H-dibenzofurocarbazolyl), the yield is over 85%, and the HPLC purity is over 98%. Mass Spectrum: Calculated 884.97; Found 884.95. Elemental analysis: calculated value C: 85.50%; H: 4.10%; N: 3.17%; O: 7.23%; tested value C: 85.52%; H: 4.11%; N: 3.16%; O: 7.21%.
Embodiment 3
[0040] Embodiment 3: the synthesis of compound 003
[0041] Concrete synthetic route is as follows:
[0042]
[0043]Weigh 33.60g of 9,10-dibromoanthracene, 111.15g of 14H-dibenzofurocarbazole, 15.26g of potassium tert-butoxide, 0.56g of palladium (II) acetate, 0.63g of tri-tert-butylphosphine, and use 250ml of toluene Dissolve and react at 84°C for 12 hours. The reaction solution was filtered, the obtained crude product was purified by silica gel chromatography, the obtained solid was recrystallized from toluene, and dried to obtain 72.99 g of light gray solid compound 9,10-bis(14H-dibenzofurocarbazolyl)anthracene , the yield is more than 84%, and the HPLC purity is greater than 98%. Mass Spectrum: Calculated 868.93; Found 868.92. Elemental analysis: calculated value C: 85.70%; H: 3.71%; N: 3.22%; O: 7.37%; tested value C: 85.72%; H: 3.72%; N: 3.21%; O: 7.35%.
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