Modifier, method of preparing the same, and modified conjugated diene-based polymer including the same

US11414440B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11414440-B2
Application numberUS-202016913390-A
CountryUS
Kind codeB2
Filing dateJun 26, 2020
Priority dateNov 21, 2016
Publication dateAug 16, 2022
Grant dateAug 16, 2022

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

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The present disclosure relates to a modifier, and more particularly, to a modifier including a compound represented by Formula 1, and a method of preparing the same. Such modifier exhibits excellent dispersibility via hydrogen bonding with an inorganic filler when mixed therewith. The present disclosure also relates to a modified conjugated diene-based polymer and a method of preparing the modified conjugated diene-based polymer by using the modifier. The resulted modified conjugated diene-based polymer exhibits excellent processability, high tensile strength, high wear resistance, low rolling resistance, and high wet skid resistance.

First claim

Opening claim text (preview).

The invention claimed is: 1. A modified conjugated diene-based polymer comprising a repeating unit derived from a conjugated diene-based monomer and, at one terminal thereof, a functional group derived from a modifier comprising a compound represented by Formula 1 below: wherein, in Formula 1, R 1 is deuterium, a substituted or unsubstituted C 1 -C 30 alkyl group, a substituted or unsubstituted C 2 -C 30 alkenyl group, a substituted or unsubstituted C 2 -C 30 alkynyl group, a substituted or unsubstituted C 1 -C 30 heteroalkyl group, a substituted or unsubstituted C 5 -C 30 cycloalkyl group, a substituted or unsubstituted C 6 -C 30 aryl group, or a substituted or unsubstituted C 3 -C 30 heterocyclic group, R 2 is deuterium, a substituted or unsubstituted C 1 -C 30 alkyl group, a substituted or unsubstituted C 1 -C 30 alkylsilyl group, a substituted or unsubstituted C 2 -C 30 alkenyl group, a substituted or unsubstituted C 2 -C 30 alkynyl group, a substituted or unsubstituted C 1 -C 30 alkoxy group, a substituted or unsubstituted C 1 -C 30 heteroalkyl group, a substituted or unsubstituted C 5 -C 30 cycloalkyl group, a substituted or unsubstituted C 6 -C 30 aryl group, a substituted or unsubstituted C 3 -C 30 heterocyclic group, or a functional group represented by Formula 1a below, R 3 is deuterium, a substituted or unsubstituted C 1 -C 30 alkyl group, a substituted or unsubstituted C 1 -C 30 alkylsilyl group, a substituted or unsubstituted C 2 -C 30 alkenyl group, a substituted or unsubstituted C 2 -C 30 alkynyl group, a substituted or unsubstituted C 1 -C 30 alkoxy group, a substituted or unsubstituted C 1 -C 30 heteroalkyl group, a substituted or unsubstituted C 5 -C 30 cycloalkyl group, a substituted or unsubstituted C 6 -C 30 aryl group, a substituted or unsubstituted C 3 -C 30 heterocyclic group, or a functional group represented by Formula 1b below, wherein, when R 1 , R 2 , and R 3 are the substituted alkyl group, the substituted alkylsilyl group, the substituted alkenyl group, the substituted alkynyl group, the substituted alkoxy group, the substituted heteroalkyl group, the substituted cycloalkyl group, the substituted aryl group, or the substituted heterocyclic group, a substituent of the substituted alkyl group, the substituted alkylsilyl group, the substituted alkenyl group, the substituted alkynyl group, the substituted alkoxy group, the substituted heteroalkyl group, the substituted cycloalkyl group, the substituted aryl group, or the substituted heterocyclic group comprises one or more selected from the group consisting of deuterium, a halogen, a hydroxyl group, a nitro group, a cyano group, a C 1 -C 30 alkyl group, a C 1 -C 30 alkylsilyl group, a C 2 -C 30 alkenyl group, a C 2 -C 30 alkynyl group, a C 1 -C 30 alkoxy group, a substituted or unsubstituted C 1 -C 30 heteroalkyl group, a C 5 -C 30 cycloalkyl group, a C 6 -C 30 aryl group, and a C 3 -C 30 heterocyclic group, and X is one heteroatom selected from the group consisting of nitrogen (N), oxygen (O), and sulfur (S), wherein, when X is N, at least one of R 2 and R 3 is necessarily the functional group of Formula 1a or 1b, and when X is O or S, only one of the R 2 and R 3 functional groups is present, wherein, when R 2 is present, R 2 is the functional group of Formula 1a, and, when R 3 is present, R 3 is the functional group of Formula 1b, wherein, in Formulae 1a and 1b, R 4 and R 7 are each independently a C 1 -C 10 alkylene group, R 5 , R 6 , R 8 , and R 9 are each independently a C 1 -C 30 alkyl group, a C 5 -C 30 cycloalkyl group, or a C 6 -C 30 aryl group, m and n are each independently an integer selected from 0, 1, 2, and 3, wherein m+n≥1, and when only one of the functional groups of Formulae 1a and 1b is present, m or n is each independently an integer selected from 1, 2, and 3. 2. The modified conjugated diene-based polymer of claim 1 , further comprising a repeating unit derived from an aromatic vinyl monomer. 3. The modified conjugated diene-based polymer of claim 1 , wherein the modified conjugated diene-based polymer has a number average molecular weight (Mn) of 10,000 g/mol to 2,000,000 g/mol. 4. The modified conjugated diene-based polymer of claim 1 , wherein the modified conjugated diene-based polymer has a molecular weight distribution (Mw/Mn) of 1.0 to 8.0. 5. The modified conjugated diene-based polymer of claim 1 , wherein the compound of Formula 1 is one selected from the group consisting of compounds represented by Formulae 1-1 to 1-12 below: wherein, in Formulae 1-1 to 1-12, R 13 is a C 1 -C 20 alkyl group. 6. A modified conjugated diene-based polymer comprising a repeating unit derived from a conjugated diene-based monomer and, at one terminal thereof, a functional group derived from a modifier comprising a compound represented by Formula 1 below and, at another terminal thereof, a functional group derived from a modification initiator represented by Formula 4 below: wherein, in Formula 1, R 1 is deuterium, a substituted or unsubstituted C 1 -C 30 alkyl group, a substituted or unsubstituted C 2 -C 30 alkenyl group, a substituted or unsubstituted C 2 -C 30 alkynyl group, a substituted or unsubstituted C 1 -C 30 heteroalkyl group, a substituted or unsubstituted C 5 -C 30 cycloalkyl group, a substituted or unsubstituted C 6 -C 30 aryl group, or a substituted or unsubstituted C 3 -C 30 heterocyclic group, R 2 is deuterium, a substituted or unsubstituted C 1 -C 30 alkyl group, a substituted or unsubstituted C 1 -C 30 alkylsilyl group, a substituted or unsubstituted C 2 -C 30 alkenyl group, a substituted or unsubstituted C 2 -C 30 alkynyl group, a substituted or unsubstituted C 1 -C 30 alkoxy group, a substituted or unsubstituted C 1 -C 30 heteroalkyl group, a substituted or unsubstituted C 5 -C 30 cycloalkyl group, a substituted or unsubstituted C 6 -C 30 aryl group, a substituted or unsubstituted C 3 -C 30 heterocyclic group, or a functional group represented by Formula 1a below, R 3 is deuterium, a substituted or unsubstituted C 1 -C 30 alkyl group, a substituted or unsubstituted C 1 -C 30 alkylsilyl group, a substituted or unsubstituted C 2 -C 30 alkenyl group, a substituted or unsubstituted C 2 -C 30 alkynyl group, a substituted or unsubstituted C 1 -C 30 alkoxy group, a substituted or unsubstituted C 1 -C 30 heteroalkyl group, a substituted or unsubstituted C 5 -C 30 cycloalkyl group, a substituted or unsubstituted C 6 -C 30 aryl group, a substituted or unsubstituted C 3 -C 30 heterocyclic group, or a functional group represented by Formula 1b below, wherein, when R 1 , R 2 , and R 3 are the substituted alkyl group, the substituted alkylsilyl group, the substituted alkenyl group, the substituted alkynyl group, the substituted alkoxy group, the substituted heteroalkyl group, the substituted cycloalkyl group, the substituted aryl group, or the substituted heterocyclic group, a substituent of the substituted alkyl group, the substituted alkylsilyl group, the substituted alkenyl group, the substituted alkynyl group, the substituted alk

Assignees

Inventors

Classifications

  • Compositions of rubber derivatives (C08L11/00, C08L13/00 take precedence) · CPC title

  • Incorporating nitrogen atoms into the molecule · CPC title

  • C07F7/1804Primary

    Compounds having Si-O-C linkages (Si-O-acyl linkages C07F7/1896) · CPC title

  • Organic solvent · CPC title

  • with vinyl-aromatic monomers · CPC title

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What does patent US11414440B2 cover?
The present disclosure relates to a modifier, and more particularly, to a modifier including a compound represented by Formula 1, and a method of preparing the same. Such modifier exhibits excellent dispersibility via hydrogen bonding with an inorganic filler when mixed therewith. The present disclosure also relates to a modified conjugated diene-based polymer and a method of preparing the modi…
Who is the assignee on this patent?
Lg Chemical Ltd
What technology area does this patent fall under?
Primary CPC classification C07F7/1804. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Aug 16 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).