Supercharge Your Innovation With Domain-Expert AI Agents!

Photosensitive resin composition containing silane coupling agent

A technology of photosensitive resin and silane coupling agent, applied in the field of photosensitive resin composition, can solve the problems of high price of phenylethynyl phthalic anhydride, unsuitable for large-scale industrial use, etc.

Active Publication Date: 2020-10-27
波米科技有限公司
View PDF9 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, phenylethynyl phthalic anhydride is expensive and not suitable for large-scale industrial use

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Photosensitive resin composition containing silane coupling agent
  • Photosensitive resin composition containing silane coupling agent
  • Photosensitive resin composition containing silane coupling agent

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0070] The preparation method of the silane coupling agent of general formula (3) is as follows:

[0071] 1) The itaconic anhydride compound represented by formula (4) and the silane compound whose terminal group is amino group represented by formula (5) perform amidation reaction to form amic acid.

[0072] 2) After the amidation reaction, carry out imidization reaction to obtain the silane coupling agent represented by the general formula (3).

[0073]

[0074] In formulas (4) and (5), R 9 , R 10 , R 11 , R 12 , R 13 The definitions are the same as those mentioned above.

[0075] Further, the amidation reaction is carried out in an aprotic polar solvent, and the effect of each aprotic polar solvent is equivalent. Considering the cost and the convenience of acquisition, preferably, the aprotic polar solvent is selected from N-methylpyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, dimethyl At least one of sulfoxide and γ-butyrolactone, preferably N-methylpy...

Synthetic example 1

[0100] Synthesis of polyimide resin A-1 (polyamide ester resin):

[0101] Under nitrogen flow, 31.02 g (0.1 mol) of 4,4'-oxydiphthalic anhydride (ODPA), N-methylpyrrolidone ( NMP) 100g, stirred and dissolved at room temperature to obtain a dianhydride solution. Take another three-necked flask equipped with a stirrer, add 2,2-bis(3-amino-4-hydroxyphenyl)hexafluoropropane (BAHF) 29.30g (0.08mol), 1,3-bis(3- Aminopropyl)-1,1,3,3-tetramethyldisiloxane (SiDA) 2.48g (0.01mol) and N-methylpyrrolidone 100g were stirred and dissolved to obtain a diamine solution. Add the diamine solution dropwise to the above-mentioned dianhydride solution, react at room temperature for 1 hour after the dropwise addition, and then react at 50°C for 2 hours. After the reaction was completed, 2.18 g (0.02 mol) of 4-aminophenol was added as an end-capping agent, and reacted at 50° C. for 2 h. Dilute 23.83 g of N,N-dimethylformamide dimethyl acetal with 45 g of NMP, and add the diluted solution dropwise...

Synthetic example 2

[0105] Synthesis of polybenzoxazole resin A-2 (polybenzoxazole precursor resin):

[0106] Under nitrogen flow, add 32.96g (0.09mol) of 2,2-bis(3-amino-4-hydroxyphenyl)hexafluoropropane (BAHF) to a 500mL three-necked flask equipped with a stirrer, dropping funnel and thermometer , 2.18g (0.02mol) of 4-aminophenol, 15.82g (0.2mol) of pyridine, and 100g of N-methylpyrrolidone (NMP) were fully dissolved, and the temperature of the solution was cooled to -15°C. Dissolve 29.51g (0.10mol) of 4,4-diphenyl ether diformyl chloride in 50g of NMP to make a solution, drop the solution into the flask with a dropping funnel, and control the reaction material below 0°C during the dropping process. After the dropwise addition was completed, the stirring reaction was continued for 6 hours under the condition of -10 to -15°C. After the reaction was completed, the reaction solution was poured into 3 L of 10 wt% methanol aqueous solution, and the polymer was precipitated to form a white precipita...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
Viscosityaaaaaaaaaa
Film thicknessaaaaaaaaaa
Login to View More

Abstract

The invention discloses a photosensitive resin composition containing a silane coupling agent. The silane coupling agent with a double bond and imide structure is introduced into the photosensitive resin composition, and by adding the silane coupling agent with the structure, the adhesiveness between the photosensitive resin composition and a base material after high-temperature thermocuring is improved.

Description

technical field [0001] The invention relates to a photosensitive resin composition containing a silane coupling agent, in particular to a silane-containing coupling agent suitable for particle shielding, surface protection, interlayer dielectric or insulation of semiconductor elements, and insulating layers of OLED elements. agent photosensitive resin composition. The photosensitive resin composition contains a silane coupling agent with a double bond and an imide structure, which can improve the adhesion between the photosensitive resin and substrates (silicon chips, ceramics, aluminum materials and other metal substrates). Background technique [0002] Since heat-resistant resins such as polyimide and polybenzoxazole have excellent heat resistance and electrical insulation, they can be used for surface protection films of semiconductor devices such as LSI (Large Scale integration; large scale integration), interlayer insulating film, etc. With the miniaturization of semi...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): G03F7/075G03F7/008G03F7/004C07F7/18
CPCG03F7/0755G03F7/0085G03F7/004C07F7/1804C07F7/1892
Inventor 李铭新公聪聪王华森陈存浩王建伟
Owner 波米科技有限公司
Features
  • R&D
  • Intellectual Property
  • Life Sciences
  • Materials
  • Tech Scout
Why Patsnap Eureka
  • Unparalleled Data Quality
  • Higher Quality Content
  • 60% Fewer Hallucinations
Social media
Patsnap Eureka Blog
Learn More