Stacked body for cof substrate, method for manufacturing such stacked body for cof substrate, and cof film carrier tape formed by using such stacked body for cof substrate
A manufacturing method and technology of laminates, which are applied in the processing of insulating substrates/layers, semiconductor/solid-state device manufacturing, printed circuit manufacturing, etc., can solve problems such as uneven thickness, difficulty in microfabrication, and difficulty in ensuring circuit linearity. , to achieve the effect of excellent electromigration resistance and high adhesion
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Synthetic example 1
[0036] Charge N-methylpyrrolidone in a reaction vessel equipped with a thermocouple and stirrer and capable of introducing nitrogen. After immersing the reaction container in the ice water put into the container, put pyromellitic anhydride (PMDA) into the reaction container, and then put 4,4'-diaminodiphenyl ether (DAPE) and 2'-methoxy - 4,4'-Diamino-N-benzoanilide (MABA). The total amount of monomers charged was 15 wt%, the molar ratio of each diamine (MABA:DAPE) was 60:40, and the molar ratio of acid anhydride and diamine was 0.98:1.0. Then, the stirring was continued, and when the temperature in the reaction container reached the range of room temperature ± 5°C, the reaction container was taken out from the ice water. Stirring was continued for 3 hours at room temperature, and the solution viscosity of the obtained polyamic acid was 15000 cps.
Synthetic example 2
[0038] Charge N-methylpyrrolidone in a reaction vessel equipped with a thermocouple and stirrer and capable of introducing nitrogen. After immersing the reaction container in the ice water put into the container, put PMDA / 3,3',4,4'-biphenyltetracarboxylic dianhydride (BTDA) into the reaction container, and then put 4,4'-diamino Diphenyl ether (DAPE). The total amount of monomers charged was 5% by weight, and the molar ratio of acid anhydride and diamine was 1.03:1.0. Then, the stirring was continued, and when the temperature in the reaction container reached the range of room temperature ± 5°C, the reaction container was taken out from the ice water. Stirring was continued for 3 hours at room temperature, and the solution viscosity of the obtained polyamic acid was 3200 cps.
Synthetic example 3
[0040] Charge N-methylpyrrolidone in a reaction vessel equipped with a thermocouple and stirrer and capable of introducing nitrogen. After immersing the reaction container in the ice water put into the container, put 3,3',4,4'-diphenylsulfonetetracarboxylic dianhydride (DSDA) and PMDA into the reaction container, and then put 1,3-bis (4-Aminophenoxy)benzene (TPE-R). The total amount of monomers charged was 15 wt%, the molar ratio of each acid anhydride (DSDA:PMDA) was 90:10, and the molar ratio of acid anhydride and diamine was 1.03:1.0. Then, the stirring was continued, and when the temperature in the reaction container reached the range of room temperature ± 5°C, the reaction container was taken out from the ice water. Stirring was continued for 3 hours at room temperature, and the solution viscosity of the obtained polyamic acid was 3200 cps.
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