Film forming composition for hard disk
US-9217096-B2 · Dec 22, 2015 · US
US2016168296A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016168296-A1 |
| Application number | US-201514960978-A |
| Country | US |
| Kind code | A1 |
| Filing date | Dec 7, 2015 |
| Priority date | Dec 10, 2014 |
| Publication date | Jun 16, 2016 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A polymer comprising recurring units having an acid generator bound to the backbone, and recurring units having an optionally acid labile group-substituted carboxyl group and/or recurring units having an optionally acid labile group-substituted hydroxyl group is obtained by polymerizing corresponding monomers under such illumination that the quantity of light of wavelength up to 400 nm is up to 0.05 mW/cm 2 . The polymer avoids photo-decomposition of the acid generator during polymerization and concomitant deprotection reaction of the acid labile group when used in positive resist compositions. A pattern with high dissolution contrast and rectangularity is formed after development.
Opening claim text (preview).
1 . A polymer comprising recurring units having an acid generator bound to the backbone, and recurring units of at least one type selected from recurring units having a carboxyl group optionally substituted with an acid labile group and recurring units having a hydroxyl group optionally substituted with an acid labile group, said polymer being obtained from polymerization of monomers corresponding to the recurring units under such illumination that the quantity of light of wavelength up to 400 nm is 0.05 mW/cm 2 or less. 2 . The polymer of claim 1 wherein the quantity of light of wavelength up to 400 nm is 0.02 mW/cm 2 or less. 3 . The polymer of claim 2 wherein the quantity of light of wavelength up to 400 nm is 0.01 mW/cm 2 or less. 4 . The polymer of claim 1 wherein the illumination is provided by an LED or organic EL. 5 . The polymer of claim 1 wherein the recurring units having an acid generator bound to the backbone are units of at least one type selected from recurring units having the formulae (1) to (3): wherein R 1 , R 5 and R 9 are each independently hydrogen or methyl, R 2 is a single bond, phenylene, —O—R— or —C(═O)—Y 0 —R—, Y 0 is oxygen or NH, R is a straight, branched or cyclic C 1 -C 6 alkylene, straight, branched or cyclic C 2 -C 6 alkenylene, or phenylene group, which may contain a carbonyl (—CO—), ester (—COO—), ether (—O—), sulfonic acid ester (—OS(O 2 )—), sulfonamide (—NH—S(O 2 )—) or hydroxyl moiety, R 3 , R 4 , R 6 , R 7 , R 8 , R 11 , R 12 and R 13 are each independently a straight, branched or cyclic C 1 -C 12 alkyl group which may contain a carbonyl, ester or ether moiety, or a C 6 -C 12 aryl, C 7 -C 20 aralkyl, or thiophenyl group, X 1 and X 2 are each independently a single bond, methylene, ethylene, phenylene, fluorinated phenylene, —O—R 14 —, or —C(═O)-Z 1 -R 14 —, Z 1 is oxygen or NH, R 14 is a straight, branched or cyclic C 1 -C 6 alkylene, alkenylene, or phenylene group, which may contain a carbonyl, ester, ether, sulfonic acid ester, sulfonamide or hydroxyl moiety, or which may be fluorinated, R 10 is a C 1 -C 4 fluoroalkyl or C 6 -C 10 fluoroaryl group, and M − is a non-nucleophilic counter ion. 6 . The polymer of claim 5 wherein at least one of R 3 and R 4 , at least one of R 6 , R 7 and R 8 , or at least one of R 11 , R 12 and R 13 is an optionally substituted phenyl group. 7 . The polymer of claim 1 wherein the recurring units having a carboxyl group optionally substituted with an acid labile group and the recurring units having a hydroxyl group optionally substituted with an acid labile group have the following formulae (4) and (5), respectively, wherein R 15 and R 17 are each independently hydrogen or methyl, R 16 and R 19 are each independently hydrogen or an acid labile group, Y 1 is a single bond, phenylene, naphthylene or —C(═O)—O—R 20 —, R 20 is a straight, branched or cyclic C 1 -C 10 alkylene group which may contain an ether, ester, lactone ring or hydroxyl moiety, or phenylene or naphthylene group, Y 2 is a single bond, a phenylene or naphthylene group which may have a nitro, cyano or halogen moiety, or —C(═O)—O—R 21 —, —C(═O)—NH—R 21 —, —O—R 21 —, or —S—R 21 —, R 21 is a straight, branched or cyclic C 1 -C 10 alkylene group which may contain an ether, ester, lactone ring or hydroxyl moiety, or a phenylene or naphthylene group which may contain a straight, branched or cyclic C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 6 -C 10 aryl, alkoxy, acyl, acyloxy, alkoxycarbonyl, nitro, cyano or halogen moiety, R 18 is a single bond, or a straight, branched or cyclic, C 1 -C 16 , di- to pentavalent, aliphatic hydrocarbon group or phenylene group, which may contain an ether or ester moiety, and m is an integer of 1 to 4. 8 . A chemically amplified resist composition comprising the polymer of claim 1 , and an organic solvent. 9 . The resist composition of claim 8 , further comprising a basic compound and/or surfactant. 10 . A pattern forming process comprising the steps of applying the resist composition of claim 8 onto a substrate, baking, exposing to high-energy radiation, and developing in a developer. 11 . The pattern forming process of claim 10 wherein the high-energy radiation is i-line, KrF excimer laser, ArF excimer laser, EB, or soft x-ray of wavelength in the range of 3 to 15 nm.
Oxygen · CPC title
Phenols or alcohols · CPC title
and containing oxygen, e.g. 2-sulfoethyl (meth)acrylate · CPC title
Liquid compositions therefor, e.g. developers · CPC title
with organic non-macromolecular light-sensitive compounds not otherwise provided for, e.g. dissolution inhibitors · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.