Organic electron transport and/or cavitation block material and synthesis method and application thereof
A technology of hole-blocking materials and organic electronics, applied in chemical instruments and methods, luminescent materials, organic chemistry, etc., can solve problems such as changes in luminescent properties, poor device performance, and stability that needs to be further improved
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Embodiment 11
[0056] Embodiment 1.1, the preparation of 4-bis(4-(2-phenyl-6-p-tolyl-3-trifluoromethylpyridine))benzene (BPTTPB)
[0057] The first step: take 2-bromo-1-(4-trifluoromethylphenyl)ethanone and pyridine with a molar ratio of 1 as raw materials, stir at room temperature for 11 hours, filter, and wash with a large amount of water to obtain the corresponding pyridine Bromide, the yield is about 90%;
[0058] The second step: under the condition of nitrogen protection, the product of the first step, terephthalaldehyde and p-methylacetophenone (molar ratio is 2:1:2) are added in the three-necked flask, and then an appropriate amount of glacial acetic acid is added and ammonium acetate, stirred vigorously, kept the temperature at 120°C to 140°C, refluxed for 24 hours, filtered out the product, and subjected to column chromatography or recrystallization to obtain the high-purity target product with a yield of about 50%.
[0059] m / z: 700.23 (100.0%), 701.23 (48.3%), 702.24 (11.2%), ...
Embodiment 21
[0069] Example 2.1, Preparation of 4-bis(4-(6-(4-biphenyl)-2-phenyl-3-trifluoromethylpyridine))benzene (BBPTPB)
[0070]
[0071] The first step: take 2-bromo-1-(4-trifluoromethylphenyl)ethanone with a molar ratio of 1, and pyridine as a raw material, stir at room temperature for 12 hours, filter, and wash with a large amount of water to obtain the corresponding pyridine Bromide, the yield is about 90%;
[0072] The second step: under the condition of nitrogen protection, the product of the first step, terephthalaldehyde and p-phenylacetophenone (molar ratio is 2:1:2) are added in the three-necked flask, and then an appropriate amount of glacial acetic acid is added and ammonium acetate, stirred vigorously, kept the temperature at 120°C to 140°C, refluxed for 24 hours, filtered out the product, and subjected to column chromatography or recrystallization to obtain the high-purity target product with a yield of about 55%.
[0073] m / z: 824.26 (100.0%), 825.27 (58.8%), 826.27...
Embodiment 34
[0074]Embodiment 3.4, the preparation of 4'-(1,4-phenylene) bis(2-phenyl-6-p-tolylpyridinecarbonitrile) (PBPTNN)
[0075] The first step: get 4-(2-bromoacetyl) benzonitrile with a molar ratio of 1, pyridine is a raw material, stir at room temperature for 10 hours, filter, and wash with a large amount of water to obtain the corresponding pyridinium bromide, with a yield of about 85%;
[0076] The second step: under the condition of nitrogen protection, the product of the first step, terephthalaldehyde and p-methylacetophenone (molar ratio is 2:1:2) are added in the three-necked flask, and then an appropriate amount of glacial acetic acid is added and ammonium acetate, stirred vigorously, kept the temperature at 120°C to 140°C, refluxed for 24 hours, filtered out the product, and subjected to column chromatography or recrystallization to obtain the high-purity target product with a yield of about 60%.
[0077] m / z: 614.25 (100.0%), 615.25 (47.9%), 616.25 (11.8%), 617.26 (1.7%...
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