Semiconductor photoresist composition and method of forming patterns using the composition
US-2026016748-A1 · Jan 15, 2026 · US
US11506975B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11506975-B2 |
| Application number | US-202016652036-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 10, 2020 |
| Priority date | Dec 26, 2019 |
| Publication date | Nov 22, 2022 |
| Grant date | Nov 22, 2022 |
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A photoresist material, a method of fabricating the same, and a color filter substrate are described. The photoresist material has an oligomer segment having a chemical structural formula of: wherein a value of n is 1 to 2.
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The invention claimed is: 1. A photoresist material, comprising an oligomer segment having a chemical structural formula of: wherein a value of n is 1 to 2; wherein, R comprises: at least one of non-conjugated linear alkanes, branched alkanes, alkoxy alkane, halogen-substituted alkane derivatives, conjugate structures linked through alkoxy and ester groups, or compounds containing heterocycles. 2. A method of fabricating a photoresist material, comprising: dissolving and stirring compound 1 in tetrahydrofuran to form a first solution, adding sodium hydride to the first solution to form a second solution, and adding compound 2 to the second solution to stir at 60° C. for 6 hours so as to obtain compound 3 after purifying and isolating; wherein a chemical structure of the compound 1 is: wherein a chemical structure of the compound 2 is: and wherein a chemical structure of the compound 3 is: 3. The method of fabricating the photoresist material according to claim 2 , wherein a molar ratio of the compound 1 to the sodium hydride is 4:1; and a molar ratio of the compound 1 to the compound 2 is 4:1.5. 4. The method of fabricating the photoresist material according claim 2 , further comprising: dissolving the compound 3 and an oligomer segment in toluene to form a first solution, and adding a catalyst to the first solution to obtain the photoresist material through a purification treatment after a reaction at room temperature for 30 minutes, wherein the oligomer segment having a chemical structural formula of: wherein a value of n is 1 or 2; wherein, R comprises: at least one of non-conjugated linear alkanes, branched alkanes, alkoxy alkane, halogen-substituted alkane derivatives, conjugate structures linked through alkoxy and ester groups, or compounds containing heterocycles, wherein a chemical structure of the photoresist material is: 5. The method of fabricating the photoresist material according to claim 4 , wherein: a molar ratio of the compound 3 to the oligomer segment is 1:1. 6. The method of fabricating the photoresist material according to claim 4 , wherein R in the oligomer segment comprises: at least one of non-conjugated linear alkanes, branched alkanes, alkoxy alkane, halogen-substituted alkane derivatives, conjugate structures linked through alkoxy and ester groups, or compounds containing heterocycles; wherein the heterocyclic compound includes at least one of a five-membered heterocyclic ring compound, a six-membered heterocyclic ring compound, or a benzoheterocyclic compound; wherein the five-membered heterocyclic compound comprises at least one of furan, thiophene, pyrrole, thiazole, and imidazole; and wherein the six-membered heterocyclic compound comprises at least one of pyridine, pyrazine, pyrimidine, and pyridazine. 7. The method of fabricating the photoresist material according to claim 6 , wherein carbon chain length in R is 1 to 3. 8. The method of fabricating the photoresist material according to claim 4 , wherein the catalyst is pentamethylcyclopentadienyl ruthenium chloride. 9. A color filter substrate, comprising a color resist layer, wherein material of the color resist layer comprises the photoresist material according to claim 1 .
containing organic substances, e.g. dyes, inks or pigments · CPC title
Filters, e.g. additive colour filters; Components for display devices · CPC title
made of organic materials, e.g. plastics (G02B1/08 takes precedence) · CPC title
characterised by the non-macromolecular additives · CPC title
Macromolecular azides; Macromolecular additives, e.g. binders {(G03F7/0085 takes precedence)} · CPC title
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