Method for carrying out a chemical reaction in an upflow reactor
US-2024042406-A1 · Feb 8, 2024 · US
US9540339B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9540339-B2 |
| Application number | US-201615005177-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 25, 2016 |
| Priority date | Aug 12, 2011 |
| Publication date | Jan 10, 2017 |
| Grant date | Jan 10, 2017 |
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A resist composition containing a compound represented by the general formula (1) or (2), a method for forming a resist pattern using the composition, a polyphenolic compound for use in the composition, and an alcoholic compound that can be derived therefrom are described.
Opening claim text (preview).
The invention claimed is: 1. A compound represented by formula (1) or formula (2): wherein R 1 are each independently a single bond or a 2n-valent hydrocarbon group having 1 to 30 carbon atoms wherein the hydrocarbon group may have a cyclic hydrocarbon group, a double bond, a heteroatom, or an aromatic group having 6 to 30 carbon atoms; R 2 are each independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group having 1 to 10 carbon atoms, an aryl group having 6 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, or a hydroxyl group and may be the same or different on the same naphthalene ring; at least two of R 2 on at least one of the naphthalene moieties is a hydroxyl group in the formula (1); at least one of R 2 is a hydroxyl group in the formula (2); n is an integer of 2 to 4; the structural formulas of the repeating units in the formulas (1) and (2) may be the same or different; in the formula (1), m 1 are each independently an integer of 1 to 7; and in the formula (2), X are each independently an oxygen atom or a sulfur atom, and m 2 are each independently an integer of 1 to 6. 2. The compound according to claim 1 , wherein the formula (1) is the general formula (1-1), and the formula (2) is the formula (2-1): wherein R 1 are each independently a single bond or a 2n-valent hydrocarbon group having 1 to 30 carbon atoms wherein the hydrocarbon group may have a cyclic hydrocarbon group, a double bond, a heteroatom, or an aromatic group having 6 to 30 carbon atoms; R 3 are each independently a hydrogen atom, a linear, branched, or cyclic alkyl group having 1 to 10 carbon atoms, an aryl group having 6 to 10 carbon atoms, or an alkenyl group having 2 to 10 carbon atoms and may be the same or different on the same naphthalene ring; the structural formulas of the repeating units in the formulas (1-1) and (2-1) may be the same or different; n is an integer of 2 to 4; in the formula (1-1), m 3 are each independently an integer of 2 to 7, m 4 are each independently an integer of 0 to 6, and m 3 +m 4 is an integer of 2 to 7; and in the formula (2-1), m 5 are each independently an integer of 1 to 6, m 6 are each independently an integer of 0 to 5, and m 5 +m 6 is an integer of 1 to 6. 3. The compound according to 1 , wherein the formula (2) is the formula (2-2): wherein R 1 is a single bond or a 2n-valent hydrocarbon group having 1 to 30 carbon atoms wherein the hydrocarbon group may have a cyclic hydrocarbon group, a double bond, a heteroatom, or an aromatic group having 6 to 30 carbon atoms; R 3 are each independently a hydrogen atom, a linear, branched, or cyclic alkyl group having 1 to 10 carbon atoms, an aryl group having 6 to 10 carbon atoms, or an alkenyl group having 2 to 10 carbon atoms and may be the same or different on the same naphthalene ring; the structural formulas of the repeating units in the formula (2-2) may be the same or different; n is an integer of 2 to 4; and in the formula (2-2), m 6 are each independently an integer of 0 to 5.
containing other rings in addition to the six-membered aromatic rings {, e.g. cyclohexylphenol} · CPC title
with organic non-macromolecular light-sensitive compounds not otherwise provided for, e.g. dissolution inhibitors · CPC title
The ring being saturated · CPC title
using aldehydes or ketones · CPC title
the ring being unsaturated · CPC title
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