Transition metal compound and catalyst composition including the same

US10189916B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10189916-B2
Application numberUS-201615538324-A
CountryUS
Kind codeB2
Filing dateJul 1, 2016
Priority dateJul 2, 2015
Publication dateJan 29, 2019
Grant dateJan 29, 2019

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present disclosure provides a novel transition metal compound having excellent structural stability together with polymerization reactivity, and thereby is useful as a catalyst in preparing an olefin-based polymer, particularly, a low density olefin-based polymer, and a catalyst composition including the same.

First claim

Opening claim text (preview).

What is claimed is: 1. A transition metal compound of the following Chemical Formula 1: wherein, in Chemical Formula 1, M is a group 4 transition metal; R is selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, a cycloalkyl group having 3 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, an arylalkyl group having 7 to 20 carbon atoms, and an alkylaryl group having 7 to 20 carbon atoms; or R and R 1 are linked to each other to form an aliphatic ring having 3 to 20 carbon atoms or an aromatic ring having 5 to 20 carbon atoms including N; R 1 to R 10 are each independently selected from the group consisting of a hydrogen atom, a halogen group, an alkyl group having 1 to 20 carbon atoms, an alkenyl group having 2 to 20 carbon atoms, a cycloalkyl group having 3 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, an arylalkyl group having 7 to 20 carbon atoms, an alkylaryl group having 7 to 20 carbon atoms, an alkoxy group having 1 to 20 carbon atoms, an aryloxy group having 6 to 20 carbon atoms, a silyl group and combinations thereof, or two or more adjacent functional groups among R 1 to R 10 are linked to each other to form an aliphatic ring having 3 to 20 carbon atoms or an aromatic ring having 6 to 20 carbon atoms; R 11 is selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, an alkenyl group having 2 to 20 carbon atoms, a cycloalkyl group having 3 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, an arylalkyl group having 7 to 20 carbon atoms, an alkylaryl group having 7 to 20 carbon atoms, a silyl group, and a metalloid radical of a group 14 metal substituted with a hydrocarbyl group having 1 to 20 carbon atoms; X 1 and X 2 are each independently selected from the group consisting of a halogen group, an alkyl group having 1 to 20 carbon atoms, an alkenyl group having 2 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, an alkylaryl group having 7 to 20 carbon atoms, an arylalkyl group having 7 to 20 carbon atoms, an alkylamino group having 1 to 20 carbon atoms, an arylamino group having 6 to 20 carbon atoms and an alkylidene group having 1 to 20 carbon atoms; R, R 1 to R 11 , X 1 and X 2 are each independently unsubstituted or substituted with one or more substituents selected from the group consisting of a halogen group, an alkyl group having 1 to 20 carbon atoms, a haloalkyl group having 1 to 20 carbon atoms, an alkenyl group having 2 to 20 carbon atoms, an alkoxy group having 1 to 20 carbon atoms, a cycloalkyl group having 3 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, an arylalkyl group having 7 to 20 carbon atoms, an alkylaryl group having 7 to 20 carbon atoms and an aryloxy group having 6 to 20 carbon atoms; n is an integer of 1 or 2, and when n is an integer of 2, R 11 's are the same as or different from each other; and wherein a dashed line to the cyclopentadienyl ring represents an η5-complex with the cyclopentadienyl ring, and a solid line to the cyclopentadienyl ring represents a σ-bond to a carbon of the cyclopentadienyl ring. 2. The transition metal compound of claim 1 , wherein R is selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 3 to 6 carbon atoms, an aryl group having 6 to 12 carbon atoms, an arylalkyl group having 7 to 12 carbon atoms, and an alkylaryl group having 7 to 12 carbon atoms; or R and R 1 are linked to each other to for a substituted or unsubstituted aliphatic ring having 4 to 6 carbon atoms or aromatic ring having 4 to 6 carbon atoms including N. 3. The transition metal compound of claim 1 , which is selected from the group consisting of compounds of the following Chemical Formulae 1a to 1c: wherein, in Chemical Formulae 1a to 1c, R 21 to R 25 are each independently selected from the group consisting of a hydrogen atom, a halogen group, an alkyl group having 1 to 20 carbon atoms, a haloalkyl group having 1 to 20 carbon atoms, an alkenyl group having 2 to 20 carbon atoms, an alkoxy group having 1 to 20 carbon atoms, a cycloalkyl group having 3 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, an arylalkyl group having 7 to 20 carbon atoms, an alkylaryl group having 7 to 20 carbon atoms, and an aryloxy group having 6 to 20 carbon atoms, or two or more adjacent functional groups among R 21 to R 25 are linked to each other to form a substituted or unsubstituted aliphatic ring having 3 to 20 carbon atoms or aromatic ring having 5 to 20 carbon atoms; R 26 is selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, a cycloalkyl group having 3 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, an arylalkyl group having 7 to 20 carbon atoms, and an alkylaryl group having 7 to 20 carbon atoms, and R 26 is also unsubstituted or substituted with one or more substituents selected from the group consisting of a halogen group, an alkyl group having 1 to 10 carbon atoms, a haloalkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, a cycloalkyl group having 3 to 12 carbon atoms, an aryl group having 6 to 12 carbon atoms, an arylalkyl group having 7 to 12 carbon atoms, an alkylaryl group having 7 to 12 carbon atoms and an aryloxy group having 6 to 12 carbon atoms; M, R 1 to R 11 , X 1 , X 2 , and n have the same definitions as in claim 1 ; and wherein a dashed line to the cyclopentadienyl ring represents an η5-complex with the cyclopentadienyl ring, and a solid line to the cyclopentadienyl ring represents a σ-bond to a carbon of the cyclopentadienyl ring. 4. The transition metal compound of claim 3 , wherein M is selected from the group consisting of titanium (Ti), zirconium (Zr) and hafnium; R 1 to R 10 are each independently selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, a cycloalkyl group having 3 to 6 carbon atoms, an aryl group having 6 to 12 carbon atoms, an arylalkyl group having 7 to 12 carbon atoms and an alkylaryl group having 7 to 12 carbon atoms, or two or more adjacent functional groups among R 1 to R 10 are linked to each other to form an aliphatic ring having 4 to 6 carbon atoms or an aromatic ring having 6 to 8 carbon atoms; R 11 is a hydrogen atom or an alkyl group having 1 to 6 carbon atoms; R 21 to R 25 are each independently selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, a cycloalkyl group having 3 to 6 carbon atoms, an aryl group having 6 to 12 carbon atoms, an arylalkyl group having 7 to 12 carbon atoms and an alkylaryl group having 7 to 12 carbon atoms, or two or more adjacent functional groups among R 21 to R 25 are linked to each other to form an aliphatic ring having 4 to 6 carbon atoms or an aromatic ring having 6 to 8 carbon atoms unsubstituted or substituted with one or more substituents selected from the group consisting of a halogen group, an alkyl group having 1 to 10 carbon atoms and a haloalkyl group having 1 to 10 carbon atoms; R 26 is selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 3 to 12 carbon atoms, an aryl group having 6 to 12 carbon atoms, an arylalkyl group having 7 to 12 carbon atoms, and an alkylaryl gro

Assignees

Inventors

Classifications

  • Copolymers of ethene with alpha-alkenes, e.g. EP rubbers · CPC title

  • C07F17/00Primary

    Metallocenes · CPC title

  • directly linked by a ring-member-to-ring-member bond · CPC title

  • condensed with rings other than six-membered or with ring systems containing such rings · CPC title

  • Ethene · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US10189916B2 cover?
The present disclosure provides a novel transition metal compound having excellent structural stability together with polymerization reactivity, and thereby is useful as a catalyst in preparing an olefin-based polymer, particularly, a low density olefin-based polymer, and a catalyst composition including the same.
Who is the assignee on this patent?
Lg Chemical Ltd
What technology area does this patent fall under?
Primary CPC classification C07F17/00. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 29 2019 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 3 related publications on this page (citations in our corpus or others sharing the same primary CPC).