Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Base reactive photoacid generators and photoresists comprising same

A photoacid generator and photoresist technology, applied in the field of photoresist compositions, can solve the problems of no beneficial effect of photoresist lithography effect, slow alkali-promoted cracking, etc., so as to improve exposure Tolerance, Defect Reduction, Effect of Low PAG Acid Diffusion

Inactive Publication Date: 2012-07-25
ROHM & HAAS ELECTRONICS MATERIALS LLC
View PDF22 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Certain PAGs disclosed in U.S. 2010 / 0081088 have an ester moiety on the PAG sulfonium cation with extremely slow base-facilitated cleavage and thus have little beneficial effect on photoresist lithographic performance

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
  • Base reactive photoacid generators and photoresists comprising same
  • Base reactive photoacid generators and photoresists comprising same
  • Base reactive photoacid generators and photoresists comprising same

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0092] The photoacid generator TPS was prepared by Equation 1 and the multi-step synthesis outlined below

[0093] NBHFA-TFPS. The detailed synthesis method is shown below.

[0094] Reaction 1

[0095]

[0096] To a solution of 4-bromo-3,3,4,4-tetrafluorobutyric acid (1.26 g, 102.7 mmol) in 150 mL of tetrahydrofuran was added carbonyldiimidazole (CDI, 16.7 g, 103.0 mmol), and the mixture was stirred at room temperature 2 Hour. The reaction mixture was heated to 70°C, then compound 2 (30 g, 102.6 mmol) was added to the reaction at 70°C under nitrogen atmosphere for 16 hours. The solvent was removed under reduced pressure and the resulting oily residue was dissolved in 200 mL of dichloromethane. The latter solution was washed twice with 200 mL of 1N HCl, once with 200 mL of water, MgSO 4 Drying and removal of the solvent under reduced pressure afforded compound 3 as a colorless oil.

[0097] In the second step, compound 3 (45 g, 85.35 mmol) was dissolved in 200 mL of ac...

Embodiment 2

[0099] Example 2: Lithographic Evaluation

[0100] The photoacid generator TPS NBHFA-TFPS of Example 1 was evaluated by photolithography with respect to conventional PAG (triphenylsulfonium perfluorobutanesulfonate). Photoresists were prepared using the components and parts described below.

[0101] The photoresist polymer (A1 ) used in the lithography evaluation (below) was prepared according to the method described below using the monomers M1-M5 described below.

[0102]

[0103] 1-ethylcyclopentyl methacrylate (ECPMA, M1; 20mmol), 1-isopropyl-adamantyl methacrylate (IAM, M2; 20mmol), 2-oxo-tetrahydromethacrylate -furan-3-yl ester (α-GBLMA, M3; 30mmol), 3-oxo-4,10-dioxo-tricyclo[5.2.1.02,6]dec-8(or 9)-ylmethacrylic acid Esters (ODOMA, M4; 20 mmol) and 3-hydroxy-adamantyl methacrylate (HAMA, M5; 10 mmol) were dissolved in 30 g of tetrahydrofuran (THF) for degassing by bubbling with nitrogen, and injected into the formulation. An additional 10 g of degassed THF was added...

Embodiment 3

[0112] Example 3: Synthesis of (4-((2,2-difluoro-3-(methacryloyloxy) (acryloyloxy)) propionyl) oxo)phenyl)-diphenylsulfonium perfluorobutanesulfonate

[0113]

[0114] 2,2-Difluoro-3-(methacryloxy)propionic acid: Add 12.6 g (100 mmol) of 2,2-bis to a mixture of 250 mL of dichloromethane and 10.1 g (100 mmol) of triethylamine Fluoro-3-hydroxypropionic acid, and the resulting mixture was placed in an ice bath. 10.5 g (100 mmol) of methacryloyl chloride was slowly added to the sesame cake, and the reaction was stirred overnight. The resulting mixture was then treated with 200 mL of 1% NaHCO 3 The solution was washed, followed by removal of solvent. The product was recrystallized from methanol to give 2,2-difluoro-3-(methacryloyloxy)propionic acid in expected good yield, which was directly used in the following synthesis without further purification.

[0115] (4-((2,2-difluoro-3-(methacryloyloxy)propionyl)oxy)phenyl)-diphenylsulfonium perfluorobutanesulfonate: to 5g (25.7mmo...

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

No PUM Login to View More

Abstract

This invention relates to new photoacid generator compounds and photoresist compositions that comprise such compounds. In particular, the invention relates to photoacid generator compounds that comprise base-cleavable groups. The present invention provides a photoacid generator compound of formula (I) or (II): (I) R<5>M<+>R<6>R<7>r<-O>3S-R<1>p-Xy-(R<2>ZwR<3>)x or (II) (P<g>-R<4>-Z<2>)g1R<5>M<+>R<6>R<7>r<-O>3S-R<1>p-Xy-(R<2>ZwR<3>)x1(R<2>Z<1>-R<4>P<g>)g2.

Description

technical field [0001] The present invention relates to novel photoacid generator compounds ("PAGs") and photoresist compositions comprising these compounds. In particular, the present invention relates to photoacid generator compounds comprising base-reactive groups. Positive and negative working chemically amplified resists comprising these PAGs, imaged under short wavelength radiation, such as below 300 nm and below 200 nm radiation, are particularly preferred. Background technique [0002] Photoresists are light-sensitive films that transfer an image to a substrate. They form negative or positive images. After coating the photoresist on the substrate, the coating is exposed through a patterned photomask to a source of activating energy, such as ultraviolet light, to form a latent image on the photoresist coating . The photomask has regions that are opaque and transparent to the exciting radiation, enabling the desired image to be transferred to the next layer of the ...

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
Patent Type & Authority Applications(China)
IPC IPC(8): C07C381/12C08F220/32C08F220/38G03F7/004G03F7/039G03F7/038G03F7/00
CPCG03F7/0382G03F7/2041G03F7/0392C07C309/06C07C2102/42C07C309/17C07D307/33C07C381/12G03F7/0045C07C63/72C07D333/46G03F7/0397C07C57/60G03F7/0046C07C2602/42G03F7/085C08F220/22C08F228/02C07C309/04C07C309/08C07C309/12C07C309/19C07C309/20C07C309/23C07C309/24C07C303/32G03F7/38
Inventor E·阿恰达李明琦C-B·徐D·王刘骢吴俊锡山田晋太郎
Owner ROHM & HAAS ELECTRONICS MATERIALS LLC
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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