Modified polyimide precursor resin, photosensitive resin composition and application thereof
A polyimide precursor and photosensitive resin technology, which is applied in the field of photolithography, can solve the problems of improving peel strength and mechanical properties, and achieve the effects of improving bonding reliability, reducing spillage, and reducing outgassing
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preparation example 1
[0082] Synthesis of hydroxyl-containing dianhydride monomer 1:
[0083]
[0084] Under the protection of nitrogen, 21.6g (0.1mol) of 3.3'-dihydroxybenzidine was dissolved in 100g of γ-butyrolactone (solution 1), cooled to -15°C, and then 44.2g of 1, 2,4-Trimellitic anhydride acid chloride was dissolved in 100 g of -butyrolactone, and added dropwise to solution 1, keeping the reaction temperature below -5°C. After the dropwise addition, the reaction was continued for 4 hours.
[0085] After concentrating the reaction product with a rotary evaporator, the concentrate was poured into 1 L of toluene to obtain a hydroxyl-containing dianhydride monomer 1 .
[0086] Structural characterization: method: Fourier transform infrared spectroscopy, characteristic peak: 1850cm -1 The characteristic peak of acid anhydride group is at 3400cm -1 The characteristic peak of -OH is at 1650cm -1 is the characteristic peak of the amide group.
preparation example 2
[0088] Synthesis of hydroxyl-containing dianhydride monomer 2:
[0089]
[0090] The difference from Preparation Example 1 is that 3,3'-dihydroxybenzidine is replaced by 5,5'-(1,4-phenylene bis(oxo))bis(2-aminophenol ), to obtain the hydroxyl-containing dianhydride monomer 2.
[0091] Structural characterization: method: Fourier transform infrared spectroscopy, characteristic peak: 1850cm -1 The characteristic peak of acid anhydride group is at 3400cm -1 The characteristic peak of -OH is at 1650cm -1 is the characteristic peak of the amide group.
preparation example 3
[0093] Synthesis of hydroxyl-containing dianhydride monomer 3:
[0094]
[0095] Synthesis method: The difference from Preparation Example 1 is that 3,3'-dihydroxybenzidine is replaced by 5,5'-(1,4-phenylene bis(oxo))bis(2 -aminobenzene-1,3-diphenol) to obtain the hydroxyl-containing dianhydride monomer 3.
[0096] Structural characterization: method: Fourier transform infrared spectroscopy, characteristic peak: 1850cm -1 The characteristic peak of acid anhydride group is at 3400cm -1 The characteristic peak of -OH is at 1650cm -1 is the characteristic peak of the amide group.
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