IP Library Granted Patent US 7,241,715
Granted Patent B2
US 7,241,715 · App. 11/436,145 · Granted Jul 10, 2007

Bridged bi-aromatic ligands, catalysts, processes for polymerizing and polymers therefrom

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Quick Facts
Patent No.
US 7,241,715
App. No.
11/436,145
Granted
Jul 10, 2007
Kind
B2
Abstract

New ligands and compositions with bridged bis-aromatic ligands are disclosed that catalyze the polymerization of monomers into polymers. These catalysts with metal centers have high performance characteristics, including higher comonomer incorporation into ethylene/olefin copolymers, where such olefins are for example, 1-octene, propylene or styrene. The catalysts also polymerize propylene into isotactic polypropylene.

Claims (19)

1. A composition, comprising:

a ligand characterized by the general formula:

wherein each of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , R 18 , R 19 , and R 20 when present is independently selected from the group consisting of hydride, halide, and optionally substituted hydrocarbyl, heteroatom-containing hydrocarbyl, alkoxy, aryloxy, silyl, boryl, phosphino, amino, alkylthio, arylthio, thioxy, seleno, nitro, and combinations thereof; optionally two or more R groups can combine together into ring structures, with such ring structures having from 3 to 100 atoms in the ring not counting hydrogen atoms; B is a bridging group having from one to 50 atoms not counting hydrogen atoms; X and X′ are the same or different and are independently selected from the group consisting of oxygen, sulfur, and —PR 30 —, where R 30 is selected from the group consisting of hydride, halide, and optionally substituted hydrocarbyl, heteroatom-containing hydrocarbyl, silyl, boryl, alkoxy, aryloxy and combinations thereof; Y and Y′ are the same or different and are independently selected from the group consisting of optionally substituted amino, phosphino, hydroxy, alkoxy, aryloxy, alkylthio, arylthio and thioxy;

a metal precursor compound characterized by the general formula M(L) n where M is a metal selected from groups 3–6 and Lanthanide elements of the Periodic Table of Elements, each L is a moiety that forms a covalent, dative or ionic bond with M; n is 1, 2, 3, 4, 5, or 6; and

optionally, at least one activator.

2. The composition of claim 1 , wherein the ligand is characterized by the formula:

wherein R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , R 18 , and R 19 are as defined above, B is as defined above, X and X′ are as defined above, and Y and Y′ are as defined above with the proviso that each of Y and Y′ include hydrogen.

3. The composition of claim 2 , wherein the ligand is characterized by the formula:

wherein each of R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 and R 9 is independently selected from the group consisting of hydride, halide, and optionally substituted alkyl, alkenyl, alkynyl, heteroalkyl, heteroalkenyl, heteroalkynyl, aryl, heteroaryl, alkoxyl, aryloxyl, silyl, boryl, phosphino, amino, alkylthio, arylthio, thioxy, seleno, nitro, and combinations thereof.

4. The composition of claim 1 , wherein each of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , R 18 , R 19 , and R 20 is independently selected from the group consisting of hydride, halide, and optionally substituted alkyl, heteroalkyl, aryl, heteroaryl, alkoxyl, aryloxyl, silyl, boryl, phosphino, amino, alkylthio, arylthio, thioxy, seleno, and nitro.

5. The composition of claim 4 , wherein each of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , R 18 , R 19 , and R 20 is independently selected from the group consisting of hydride, halide, and optionally substituted alkyl, heteroalkyl, aryl, heteroaryl, alkoxyl, aryloxyl, silyl, amino, alkylthio, arylthio and thioxy.

6. The composition of claim 3 , wherein each R 2 is not hydrogen.

7. The composition of claim 6 , wherein each R 2 is independently selected from the group consisting of optionally substituted aryl and heteroaryl.

8. The composition of claim 3 , wherein the bridging group B is selected from the group consisting of optionally substituted divalent hydrocarbyl and divalent heteroatom containing hydrocarbyl.

9. The composition of claim 8 , wherein B is selected from the group consisting of optionally substituted divalent alkyl, alkenyl, alkynyl, heteroalkyl, heteroalkenyl, heteroalkynyl, aryl, heteroaryl and silyl.

10. The composition of claim 8 , wherein B is represented by the general formula -(Q″R 40 2-z″ ) z′ — wherein each Q″ is either carbon or silicon and each R 40 may be the same or different from the others such that each R 40 is selected from the group consisting of hydride and optionally substituted hydrocarbyl and heteroatom containing hydrocarbyl, and optionally two or more R 40 groups may be joined into a ring structure having from 3 to 50 atoms in the ring structure not counting hydrogen atoms; z′ is an integer from 1 to 10; and z″ is 0, 1 or 2.

11. The composition of any of claim 1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 or 10 wherein M is selected from the group consisting of Hf, Zr and Ti.

12. The composition of claim 3 , wherein R 7 and R 8 are independently selected from the group consisting of halo, alkoxy, aryloxy, and amino.

13. The composition of claim 3 , wherein at least one L is an anion.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2016
From: FREESLATE, INC.
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 039758/0897 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2010
From: SYMYX SOLUTIONS, INC.
To: FREESLATE, INC.
Reel/Frame 024057/0911 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 13, 2009
From: SYMYX TECHNOLOGIES, INC.
To: SYMYX SOLUTIONS, INC.
Reel/Frame 022939/0564 →