Method for producing polymer for electronic material and polymer for electronic material obtained by the production method
US-2018134819-A1 · May 17, 2018 · US
US2020207902A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2020207902-A1 |
| Application number | US-201916724777-A |
| Country | US |
| Kind code | A1 |
| Filing date | Dec 23, 2019 |
| Priority date | Dec 26, 2018 |
| Publication date | Jul 2, 2020 |
| Grant date | — |
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A polymer, a hardmask composition, and a method of forming patterns, the polymer including structural units obtained by a reaction of a reaction mixture that includes a substituted or unsubstituted indole compound, a first aromatic aldehyde compound including a substituted or unsubstituted C3 to C20 branched alkyl group thereon, and a second aromatic aldehyde compound that is different from the first aromatic aldehyde compound.
Opening claim text (preview).
What is claimed is: 1 . A polymer comprising structural units obtained by a reaction of a reaction mixture that includes: a substituted or unsubstituted indole compound, a first aromatic aldehyde compound including a substituted or unsubstituted C3 to C20 branched alkyl group thereon, and a second aromatic aldehyde compound that is different from the first aromatic aldehyde compound. 2 . The polymer as claimed in claim 1 , wherein the indole compound is represented by Chemical Formula 1: wherein, in Chemical Formula 1, Z 1 is hydrogen, a hydroxy group, a halogen atom, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C1 to C30 cycloalkyl group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted C2 to C30 alkynyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C1 to C30 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof, Z 2 and Z 3 are independently a hydroxy group, a halogen atom, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C1 to C30 cycloalkyl group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted C2 to C30 alkynyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C1 to C30 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof, m is an integer of 0 to 4, and n is an integer of 0 to 2. 3 . The polymer as claimed in claim 1 , wherein the substituted or unsubstituted C3 to C20 branched alkyl group is a substituted or unsubstituted tert-butyl group. 4 . The polymer as claimed in claim 1 , wherein the first aromatic aldehyde compound includes a substituted or unsubstituted aromatic ring moiety of Group 1: 5 . The polymer as claimed in claim 1 , wherein the first aromatic aldehyde compound is a benzaldehyde substituted with a C3 to C20 branched alkyl group, a naphthaldehyde substituted with a C3 to C20 branched alkyl group, an anthracenecarboxaldehyde substituted with a C3 to C20 branched alkyl group, or a pyrenecarboxaldehyde substituted with a C3 to C20 branched alkyl group. 6 . The polymer as claimed in claim 1 , wherein the second aromatic aldehyde compound includes a substituted or unsubstituted aromatic ring moiety of Group 2: 7 . The polymer as claimed in claim 1 , wherein the second aromatic aldehyde compound includes a C6 to C30 aromatic ring substituted at least one hydroxy group. 8 . The polymer as claimed in claim 1 , wherein at least one of the first aromatic aldehyde compound and the second aromatic aldehyde compound includes a condensed ring. 9 . The polymer as claimed in claim 1 , wherein: the first aromatic aldehyde compound is a benzaldehyde substituted with a C3 to C20 branched alkyl group, a naphthaldehyde substituted with a C3 to C20 branched alkyl group, an anthracenecarboxaldehyde substituted with a C3 to C20 branched alkyl group, or a pyrenecarboxaldehyde substituted with a C3 to C20 branched alkyl group, and the second aromatic aldehyde compound is a substituted or unsubstituted pyrenecarboxaldehyde. 10 . The polymer as claimed in claim 1 , wherein: the indole compound is included in the reaction mixture in an amount of about 1 mol % to about 50 mol %, the first aromatic aldehyde compound is included in the reaction mixture in an amount of about 1 mol % to about 80 mol %, and the second aromatic aldehyde compound is included in the reaction mixture in an amount of about 1 mol % to about 80 mol %, all mol % being based on a total number of moles of the indole compound, the first aromatic aldehyde compound, and the second aromatic aldehyde compound in the reaction mixture. 11 . A hardmask composition, comprising: the polymer as claimed in claim 1 , and a solvent. 12 . A method of forming patterns, the method comprising: applying the hardmask composition as claimed in claim 11 on a material layer and heat-treating the same to form a hardmask layer, forming a photoresist layer on the hardmask layer, exposing and developing the photoresist layer to form a photoresist pattern, selectively removing the hardmask layer using the photoresist pattern to expose a portion of the material layer, and etching the exposed portion of the material layer.
with heterocyclic compounds · CPC title
Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor (using photoresist structures for special production processes, see the relevant places, e.g. B44C, H10P76/00, H05K) · CPC title
Photosensitive materials (G03F7/12, G03F7/14 take precedence) · CPC title
having cover layers or intermediate layers, e.g. subbing layers {(G03F7/091 - G03F7/093, B41N3/03 take precedence)} · CPC title
of masks comprising organic materials · CPC title
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