Chemically amplified positive resist composition and resist pattern forming process
US-12164231-B2 · Dec 10, 2024 · US
US10719015B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10719015-B2 |
| Application number | US-201815950630-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 11, 2018 |
| Priority date | Apr 17, 2017 |
| Publication date | Jul 21, 2020 |
| Grant date | Jul 21, 2020 |
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A laminate comprising a thermoplastic film and a positive resist film is provided, the positive resist film comprising (A) a novolak resin-naphthoquinone diazide (NQD) base resin composition, (B) a polyester, and (C) 3-30 wt % of an organic solvent. The resist film may be transferred to a stepped support without forming voids.
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The invention claimed is: 1. A positive resist film laminate comprising a thermoplastic film as a first support and a novolak resin-naphthoquinone diazide (NQD) base positive resist film thereon, said novolak resin-NQD base positive resist film comprising (A) a novolak resin-NQD base resin composition, (B) a polyester, and (C) 3 to 30% by weight of an organic solvent, the novolak resin-NQD base resin composition (A) comprising (A-1) a novolak resin having phenolic hydroxyl groups wherein some or all hydrogen atoms of the phenolic hydroxyl groups are substituted by 1,2-naphthoquinone diazidosulfonyl groups, (A-2) a novolak resin having phenolic hydroxyl groups wherein some or all hydrogen atoms of the phenolic hydroxyl groups are substituted by 1,2-naphthoquinone diazidosulfonyl groups, and a novolak resin having unsubstituted phenolic hydroxyl groups, (A-3) a novolak resin having phenolic hydroxyl groups wherein some or all hydrogen atoms of the phenolic hydroxyl groups are substituted by 1,2-naphthoquinone diazidosulfonyl groups, and a 1,2-naphthoquinone diazidosulfonic acid ester, (A-4) a novolak resin having phenolic hydroxyl groups wherein some or all hydrogen atoms of the phenolic hydroxyl groups are substituted by 1,2-naphthoquinone diazidosulfonyl groups, a novolak resin having unsubstituted phenolic hydroxyl groups, and a 1,2-naphthoquinone diazidosulfonic acid ester, or (A-5) a novolak resin having unsubstituted phenolic hydroxyl groups and a 1,2-naphthoquinone diazidosulfonic acid ester, wherein the polyester (B) is a condensate of a polyfunctional carboxylic acid with a polyhydric alcohol or a condensate of a polyfunctional carboxylic anhydride with a polyhydric alcohol. 2. The laminate of claim 1 wherein the polyester (B) is a polyester based on a polyfunctional carboxylic acid having 2 to 6 carboxyl groups. 3. A pattern forming process comprising the steps of: (1) transferring the novolak resin-NQD base positive resist film of the laminate of claim 1 to a second support, (2) exposing the resist film to UV radiation, and (3) developing the resist film in an alkaline aqueous solution. 4. The process of claim 3 wherein the step (1) further includes pre-baking the resist film after the transfer. 5. The process of claim 3 wherein the step (2) further includes post-exposure baking. 6. The process of claim 3 , further comprising the step (4) of forming a metal plating layer on the second support by electroplating or electroless plating, subsequent to the step (3). 7. A positive resist film laminate comprising a thermoplastic film as a first support and a novolak resin-naphthoquinone diazide (NQD) base positive resist film thereon, said novolak resin-NQD base positive resist film comprising (A) a novolak resin-NQD base resin composition, (B) a polyester, and (C) 3 to 30% by weight of an organic solvent, the novolak resin-NQD base resin composition (A) comprising (A-1) a novolak resin having phenolic hydroxyl groups wherein some or all hydrogen atoms of the phenolic hydroxyl groups are substituted by 1,2-naphthoquinone diazidosulfonyl groups, (A-2) a novolak resin having phenolic hydroxyl groups wherein some or all hydrogen atoms of the phenolic hydroxyl groups are substituted by 1,2-naphthoquinone diazidosulfonyl groups, and a novolak resin having unsubstituted phenolic hydroxyl groups, (A-3) a novolak resin having phenolic hydroxyl groups wherein some or all hydrogen atoms of the phenolic hydroxyl groups are substituted by 1,2-naphthoquinone diazidosulfonyl groups, and a 1,2-naphthoquinone diazidosulfonic acid ester, (A-4) a novolak resin having phenolic hydroxyl groups wherein some or all hydrogen atoms of the phenolic hydroxyl groups are substituted by 1,2-naphthoquinone diazidosulfonyl groups, a novolak resin having unsubstituted phenolic hydroxyl groups, and a 1,2-naphthoquinone diazidosulfonic acid ester, or (A-5) a novolak resin having unsubstituted phenolic hydroxyl groups and a 1,2-naphthoquinone diazidosulfonic acid ester, wherein the polyester (B) is alkali soluble. 8. The laminate of claim 1 , further comprising (D) a surfactant.
Coating processes; Apparatus therefor (applying coatings to base materials in general B05; applying photosensitive compositions to base for photographic purposes G03C1/74) · CPC title
the macromolecular compound being present in a chemically amplified positive photoresist composition · CPC title
characterised by the polymeric binders or the macromolecular additives other than the macromolecular quinonediazides · CPC title
Finishing the coated layer, e.g. drying, baking, soaking · CPC title
Treatment after imagewise removal, e.g. baking · CPC title
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