Positive Photosensitive Resin Composition
A technology of photosensitive resin and composition, applied in optics, opto-mechanical equipment, instruments, etc., can solve the problems of insufficient storage stability and low sensitivity, and achieve the effects of excellent sensitivity stability and excellent adhesion
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment
[0092]Examples and the like are given below to illustrate the present invention, but the present invention is not limited to these examples. In addition, the evaluation of the positive photosensitive resin composition in an Example was performed by the following method.
[0093] (1) Storage stability evaluation of sensitivity
[0094] Preparation of photosensitive resin film
[0095] A positive-type photosensitive resin composition (hereinafter referred to as varnish) is coated on a 6-inch silicon wafer so that the film thickness after prebaking is 8 μm, and then a hot plate (coating and developing device Mark- 7) It prebaked at 120 degreeC for 3 minutes, and obtained the photosensitive resin film.
[0096] Film Thickness Measuring Method
[0097] Using Lambda Ace STM-602 manufactured by Dainippon Screen Manufacturing Co., Ltd., the film after prebaking and development was measured with a refractive index of 1.629, and the cure film was measured with a refractive index of 1...
Synthetic example 1
[0110] Synthesis Example 1 Synthesis of an acid anhydride (a) having a hydroxyl group
[0111] Under a stream of dry nitrogen, 18.3 g (0.05 mol) of 2,2-bis(3-amino-4-hydroxyphenyl)hexafluoropropane (BAHF) and 34.2 g (0.3 mol) of allyl glycidyl ether were dissolved in 100g of γ-butyrolactone (GBL), cooled to -15°C. 22.1 g (0.11 mol) of trimellitic anhydride acid chloride dissolved in 50 g of GBL was dropped therein so that the temperature of the reaction liquid did not exceed 0°C. After completion of dripping, it was made to react at 0 degreeC for 4 hours. This solution was concentrated with a rotary evaporator and poured into 1 L of toluene to obtain an acid anhydride (a) having a hydroxyl group represented by the following formula.
[0112]
Synthetic example 2
[0113] Synthesis Example 2 Synthesis of diamine compound (b) having a hydroxyl group
[0114] 18.3 g (0.05 mol) of BAHF was dissolved in 100 mL of acetone and 17.4 g (0.3 mol) of propylene oxide, and cooled to -15°C. 20.4 g (0.11 mol) of 3-nitrobenzoyl chloride dissolved in 100 mL of acetone was added dropwise thereto. After completion|finish of dripping, it was made to react at -15 degreeC for 4 hours, and it returned to room temperature after that. The precipitated white solid was filtered and vacuum-dried at 50°C.
[0115] Put 30g of solid into a 300mL stainless steel autoclave, disperse it in 250mL of methyl cellosolve, and add 2g of 5% palladium-carbon. Hydrogen is introduced into it with a balloon, and the reduction reaction is carried out at room temperature. After about 2 hours, it was confirmed that the balloon was no longer deflated, and the reaction was terminated. After completion of the reaction, the catalyst palladium compound was removed by filtration, and c...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com