Base-generating agent, photosensitive resin composition, material for pattern-forming comprising said photosensitive resin composition, pattern-forming method using said photosensitive resin composition, and article
A technology of photosensitive resin and alkali generator, applied to alkali generator, photosensitive resin composition, material for pattern formation formed from the photosensitive resin composition, pattern formation and articles using the photosensitive resin composition It can solve the problems such as the inability to obtain polyimide physical properties and the structural limitations of polyimide precursors, and achieve the effects of large solubility contrast, excellent sensitivity, and excellent sensitivity
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[0369] Hereinafter, the present invention will be specifically described with reference to examples. The present invention is not limited by these descriptions. In addition, in an Example, "part" means a "weight part" unless otherwise indicated. pass 1 H NMR measurement to confirm the chemical structure of the produced base generator.
[0370] In addition, each measurement and experiment were performed using the apparatus shown below.
[0371] 1 H NMR measurement: JEOL JNM-LA400WB manufactured by JEOL Ltd.
[0372] Manual exposure: manufactured by Dainippon Research Institute, MA-1100
[0373] Absorbance measurement: Shimadzu Corporation, ultraviolet-visible spectrophotometer UV-2550
[0374] Measurement of temperature at 5% weight loss: Shimadzu Corporation, differential thermal-thermogravimetric simultaneous measuring device DTG-60
[0375] Infrared absorption spectrometry: FTS7000, manufactured by Varian Technologies Japan limited
[0376] Heating of the coating fil...
Synthetic example 1
[0377] (Synthesis example 1: Synthesis of polyimide precursor)
[0378] 10.0 g (50 mmol) of bis(4-aminophenyl) ether was dropped into a 300 mL three-necked flask, dissolved in 105.4 mL of dehydrated N,N-dimethylacetamide (DMAc) and heated under a nitrogen stream. Stir while cooling in an ice bath. Add 14.7 g (50 mmol) of 3,3',4,4'-biphenyltetracarboxylic acid 3,4:3',4'-dianhydride little by little, and stir in an ice bath for 5 hours after the addition , Utilize the dehydrated diethyl ether to carry out reprecipitation to the solution, dry the precipitate at room temperature and under reduced pressure for 17 hours, and quantitatively obtain polyamic acid (polyamic acid) with a weight average molecular weight of 10,000 in the form of white solid Amine Precursor (1)).
Synthetic example 2
[0379] (Synthesis example 2: Synthesis of metal alkoxide condensate)
[0380] 5 g of phenyltriethoxysilane, 10 g of triethoxysilane, 0.05 g of ammonia water, 5 ml of water, and 50 ml of propylene glycol monomethyl ether acetate were added to a 100 ml flask with a condenser. The solution was stirred with a semicircular mechanical stirrer, and reacted at 70° C. for 6 hours using a mantle heater. Next, ethanol and residual water produced in the condensation reaction with water were removed using an evaporator. After completion|finish of reaction, the flask was left to room temperature, and the condensate (alkoxysilane condensate (1)) of an alkoxysilane was prepared.
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