Polyimide
一种聚酰亚胺、独立地的技术,应用在仪器、电气元件、有机化学等方向,能够解决溶剂溶解性低、绝缘性高、溶液稳定性和薄膜性能未必能够满足等问题,达到薄膜性能极好、低电阻值的效果
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Synthetic example 1
[0078] [Synthesis Example 1] Synthesis of 1-nitro-2,3-diaminobenzene
[0079]
[0080] Dissolve 14g of commercially available 1-amino-2,5-dinitrobenzene in 225ml of methanol, and add 60g of sodium sulfide and 21g of sodium bicarbonate into 240g of water with a dropping funnel while maintaining the reaction temperature at 60°C to form The solution. After the addition was complete, it was stirred at 60° C. for an additional hour. After the reaction was completed, it was cooled to room temperature and filtered.
[0081] M / z (FD+) 153 (calculated value 153.1396)
[0082] 1 H-NMR (CDCl 3 , δppm) 7.72, 7.70, 7.24, 6.92, 6.62, 6.60, 6.59, 5.92, 3.40
[0083] Yield 7.79g (66.5% yield)
Synthetic example 21
[0084] [Synthesis Example 2] Synthesis of 1,4-bis[5-nitro-3-phenylquinoxalin-2-yl]benzene
[0085]
[0086]3.06 g of 1-nitro-2,3-diaminobenzene and 1,4-bisbenzoyl (1,4-bisbenzil) were dispersed in acetic acid-methanol (1:1) mixed solvent, under nitrogen atmosphere, in Stir at 60°C for 3.5 hours. After the reaction was completed, it was cooled to room temperature, and then the precipitate was filtered, washed with methanol, and dried to obtain the target product.
[0087] M / z(FD+) 575 (calculated value 576.56)
[0088] Yield 6.35g (yield 95%)
Embodiment 1
[0089] [Example 1] 1, the synthesis of 4-bis [5-amino-3-phenylquinoxalin-2-yl] benzene
[0090]
[0091] 2.37 g of 1,4-bis[5-nitro-3-phenylquinoxalin-2-yl]benzene was dissolved in 300 g of THF, and after nitrogen substitution, 1.14 g of PdC was added. After the reaction system was replaced with nitrogen, a predetermined amount of hydrogen was added, followed by stirring at room temperature for 48 hours. After the reaction, the precipitate was filtered out, washed with methanol until the washing liquid was not colored, and dried. Then, the filtered crude product was separated and purified with a silica gel column to obtain the target product. In this case, chloroform was used as the eluent.
[0092] M / z (FD+) 515 (calculated value 516.59)
[0093] Yield 1.05g (yield 49.5%)
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