Aromatic underlayer
US-2020142309-A1 · May 7, 2020 · US
US12411409B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12411409-B2 |
| Application number | US-202117245326-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 30, 2021 |
| Priority date | Nov 2, 2018 |
| Publication date | Sep 9, 2025 |
| Grant date | Sep 9, 2025 |
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Compounds having three or more alkynyl moieties substituted with an aromatic moiety having one or more of certain substituents are useful in forming underlayers useful in semiconductor manufacturing processes.
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What is claimed is: 1. A method comprising: (a) providing an electronic device substrate; (b) coating a layer of a coating composition comprising one or more curable compounds on a surface of the electronic device substrate, wherein the one or more curable compounds comprise an aromatic core chosen from a C 5-6 aromatic ring and a C 9-30 fused aromatic ring system and three or more substituents of formula (1) wherein at least two substituents of formula (1) are attached to the aromatic core; and wherein Ar 1 is an aromatic ring or fused aromatic ring system having from 5 to 30 carbons; Z is a substituent chosen from OR 1 , protected hydroxyl, carboxyl, protected carboxyl, SR 1 , protected thiol, —O—C(═O)—C 1-6 -alkyl, halogen, and NHR 2 ; each R 1 is chosen from H, C 1-10 alkyl, C 2-10 unsaturated hydrocarbyl, and C 5-30 aryl; each R 2 is chosen from H, C 1-10 alkyl, C 2-10 unsaturated hydrocarbyl, C 5-30 aryl, C(═O)—R 1 , and S(═O) 2 —R 1 ; x is an integer from 1 to 4; and * denotes the point of attachment to the aromatic core; wherein Ar 1 is not further substituted beyond the Z substituent(s) and the alkyne-containing substituent; provided that no substituents of formula (1) are in an ortho position to each other on the same ring of the aromatic core; (c) curing the layer of the curable compound to form an underlayer; (d) coating a layer of a photoresist on the underlayer; (e) exposing the photoresist layer to actinic radiation through a mask; (f) developing the exposed photoresist layer to form a resist pattern; and (g) transferring the pattern to the underlayer to expose portions of the electronic device substrate. 2. The method of claim 1 further comprising the steps of patterning the substrate; and then removing the patterned underlayer. 3. The method of claim 1 further comprising the step of coating one or more of a silicon-containing layer, an organic antireflective coating layer and a combination thereof over the underlayer before step (d). 4. The method of claim 3 further comprising the step of transferring the pattern to the one or more of the silicon-containing layer, the organic antireflective coating layer and the combination thereof after step (f) and before step (g). 5. The method of claim 1 wherein each Z is independently chosen from OR 1 , protected hydroxyl, carboxyl, protected carboxyl, SH, fluorine and NR 2 . 6. The method of claim 1 wherein aromatic core is chosen from pyridine, benzene, naphthalene, quinoline, isoquinoline, anthracene, phenanthrene, pyrene, coronene, triphenylene, chrysene, phenalene, benz[a]anthracene, dibenz[a,h]anthracene, and benzo[a]pyrene. 7. The method of claim 1 wherein each Ar 1 is independently chosen from pyridine, benzene, naphthalene, quinoline, isoquinoline, anthracene, phenanthrene, pyrene, coronene, triphenylene, chrysene, phenalene, benz[a]anthracene, dibenz[a,h]anthracene, and benzo[a]pyrene. 8. The method of claim 1 wherein the coating composition further comprises one or more of an organic solvent, a curing agent, and a surface leveling agent. 9. An electronic device comprising an electronic device substrate having a layer of a polymer comprising as polymerized units one or more curable compounds on a surface of the electronic device substrate, wherein the one or more curable compounds comprise an aromatic core chosen from a C 5-6 aromatic ring and a C 9-30 fused aromatic ring system and three or more substituents of formula (1) wherein at least two substituents of formula (1) are attached to the aromatic core; and wherein Ar 1 is an aromatic ring or fused aromatic ring system having from 5 to 30 carbons; Z is a substituent chosen from OR 1 , protected hydroxyl, carboxyl, protected carboxyl, SR 1 , protected thiol, —O—C(═O)—C 1-6 -alkyl, halogen, and NHR 2 ; each R 1 is chosen from H, C 1-10 alkyl, C 2-10 unsaturated hydrocarbyl, and C 5-30 aryl; each R 2 is chosen from H, C 1-10 alkyl, C 2-10 unsaturated hydrocarbyl, C 5-30 aryl, C(═O)—R 1 , and S(═O) 2 -R 1 ; x is an integer from 1 to 4; and * denotes the point of attachment to the aromatic core; wherein Ar 1 is not further substituted beyond the Z substituent(s) and the alkyne-containing substituent; provided that no substituents of formula (1) are in an ortho position to each other on the same ring of the aromatic core. 10. The method of claim 5 wherein each Z is OH. 11. The method of claim 1 wherein each Ar 1 is independently chosen from pyridine, benzene, naphthalene, quinoline, isoquinoline, anthracene, phenanthrene, pyrene, coronene, triphenylene, chrysene, phenalene, benz[a]anthracene, dibenz[a,h]anthracene, and benzo[a]pyrene. 12. The method of claim 11 wherein each Ar 1 is benzene. 13. The method of claim 12 wherein each Z is OH.
Anti-reflective coatings · CPC title
in non photosensitive layers or as additives, e.g. for dry lithography · CPC title
characterised by antireflection means or light filtering or absorbing means, e.g. anti-halation, contrast enhancement · CPC title
having cover layers or intermediate layers, e.g. subbing layers {(G03F7/091 - G03F7/093, B41N3/03 take precedence)} · CPC title
Multilayer resist systems, e.g. planarising layers · CPC title
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