Resist patterning method and resist material
US-2018356731-A1 · Dec 13, 2018 · US
US12265333B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12265333-B2 |
| Application number | US-202117482557-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 23, 2021 |
| Priority date | Mar 28, 2019 |
| Publication date | Apr 1, 2025 |
| Grant date | Apr 1, 2025 |
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The composition contains: a compound which has a group represented by formula (1); and a solvent. In the formula (1), R 1 and R 2 each independently represent a substituted or unsubstituted aryl group having 6 to 30 ring atoms or a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms; R 3 represents a hydrogen atom or a substituted or unsubstituted monovalent aliphatic hydrocarbon group having 1 to 10 carbon atoms; and * denotes a bonding site to a part other than the group represented by the following formula (1) in the compound.
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What is claimed is: 1. A composition comprising: a compound represented by formula (2); and a solvent, wherein, in the formula (1), R 1 and R 2 each independently represent a substituted or unsubstituted aryl group having 6 to 30 ring atoms or a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms; at least one of R 1 and R 2 represents a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthryl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted phenanthryl group, a substituted or unsubstituted phenalenyl group, a substituted or unsubstituted pyrenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted triphenylenyl group, a substituted or unsubstituted tetracenyl group, a substituted or unsubstituted perylenyl group, a substituted or unsubstituted picenyl group, a substituted or unsubstituted pentacenyl group, a substituted or unsubstituted hexacenyl group, a substituted or unsubstituted coronenyl group, a substituted or unsubstituted trinaphthylenyl group, a substituted or unsubstituted heptacenyl group, or a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms; R 3 represents a hydrogen atom or a substituted or unsubstituted monovalent aliphatic hydrocarbon group having 1 to 10 carbon atoms; n is an integer of 2 to 10, wherein a plurality of R 1 s are identical or different from each other, a plurality of R 2 s are identical or different from each other, and a plurality of R 3 s are identical or different from each other; and R 4 represents an organic group having a valency of n and having an aromatic ring which has 5 to 40 ring atoms. 2. The composition according to claim 1 , wherein the substituted or unsubstituted monovalent aliphatic hydrocarbon group which is represented by R 3 is a substituted or unsubstituted monovalent chain hydrocarbon group. 3. The composition according to claim 1 , wherein R 3 represents a hydrogen atom. 4. The composition according to claim 1 , wherein at least one of R 1 and R 2 represents a group represented by formula (3): wherein, in the formula (3), R 5 represents a hydrogen atom or a monovalent aliphatic hydrocarbon group having 1 to 10 carbon atoms; Ar represents a group obtained by removing (m+1) hydrogen atoms from an aromatic ring having 6 to 30 ring atoms; m is an integer of 1 to 3; ** denotes a binding site to a carbon atom to which R 1 or R 2 bonds in the formula (1); and in a case in which m is no less than 2, a plurality of R 5 s are identical or different from each other. 5. The composition according to claim 1 , wherein a proportion of hydrogen atoms with respect to all atoms constituting the compound is no greater than 7% by mass. 6. The composition according to claim 1 , wherein a molecular weight of the compound is no less than 300 and no greater than 3,000. 7. A method of forming a resist underlayer film, the method comprising: applying the composition according to claim 1 directly or indirectly on a substrate. 8. A method of producing a patterned substrate, the method comprising: forming a resist underlayer film directly or indirectly on a substrate by applying the composition according to claim 1 ; forming a resist pattern directly or indirectly on the resist underlayer film; and carrying out etching using the resist pattern as a mask. 9. The method according to claim 8 , further comprising, before forming the resist pattern, forming a silicon-containing film directly or indirectly on the resist underlayer film formed. 10. A compound represented by formula (2): wherein, in the formula (2), R 1 and R 2 each independently represent a substituted or unsubstituted aryl group having 6 to 30 ring atoms or a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms; at least one of R 1 and R 2 represents a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthryl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted phenanthryl group, a substituted or unsubstituted phenalenyl group, a substituted or unsubstituted pyrenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted triphenylenyl group, a substituted or unsubstituted tetracenyl group, a substituted or unsubstituted perylenyl group, a substituted or unsubstituted picenyl group, a substituted or unsubstituted pentacenyl group, a substituted or unsubstituted hexacenyl group, a substituted or unsubstituted coronenyl group, a substituted or unsubstituted trinaphthylenyl group, a substituted or unsubstituted heptacenyl group, or a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms; R 3 represents a hydrogen atom or a substituted or unsubstituted monovalent aliphatic hydrocarbon group having 1 to 10 carbon atoms; n is an integer of 2 to 10, wherein a plurality of R 1 s are identical or different from each other, a plurality of R 2 s are identical or different from each other, and a plurality of R 3 s are identical or different from each other; and R 4 represents an organic group having a valency of n and having an aromatic ring which has 5 to 40 ring atoms. 11. The composition according to claim 1 , wherein at least one of R 1 and R 2 represents a substituted or unsubstituted fluorenyl group or a substituted or unsubstituted pyrenyl group. 12. The compound according to claim 10 , wherein at least one of R 1 and R 2 represents a substituted or unsubstituted fluorenyl group or a substituted or unsubstituted pyrenyl group. 13. The compound according to claim 10 , wherein the substituted or unsubstituted monovalent aliphatic hydrocarbon group which is represented by R 3 is a substituted or unsubstituted monovalent chain hydrocarbon group. 14. The compound according to claim 10 , wherein R 3 represents a hydrogen atom. 15. The composition according to claim 1 , wherein R 4 represents a group represented by formula (II-1), formula (II-2), formula (II-3), formula (II-4), or formula (II-5): wherein ** denotes a binding site to a carbon atom to which R 4 in the formula (2) bonds. 16. The compound according to claim 10 , wherein R 4 represents a group represented by formula (II-1), formula (II-2), formula (II-3), formula (II-4), or formula (II-5): wherein *** denotes a binding site to a carbon atom to which R 4 in the formula (2) bonds.
of aldehydes with phenols · CPC title
with phenol · CPC title
with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms · CPC title
with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to the ring nitrogen atoms · CPC title
having amino groups bound to two or three six-membered aromatic rings · CPC title
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