Synthesis of aryl coupled bis phenoxides and their use in olefin polymerization catalyst systems with activator-supports

Patent metadata

Field	Value
Publication number	US-9663594-B2
Application number	US-201615176204-A
Country	US
Kind code	B2
Filing date	Jun 8, 2016
Priority date	May 15, 2014
Publication date	May 30, 2017
Grant date	May 30, 2017

Abstract

Disclosed herein are methods of making bis(phenol) ligand compounds and transition metal bis(phenolate) compounds. The transition metal bis(phenolate) compounds can be used as components in catalyst systems for the polymerization of olefins.

First claim

I claim:

1. A catalyst composition comprising a transition metal bis(phenolate) compound, an activator-support comprising a solid oxide treated with an electron-withdrawing anion, and an optional co-catalyst, wherein the transition metal bis(phenolate) compound has the formula:

wherein:
R 2 , R 3 , R 4 , and R 5 independently are H or a C 1 to C 18 hydrocarbyl or halogenated hydrocarbyl group;

is a substituted or unsubstituted, saturated or unsaturated, C 4 to C 8 heterocyclic group, wherein each R A independently is a C 1 to C 18 hydrocarbyl or halogenated hydrocarbyl group, and m is 0, 1, 2, or 3;
M is Ti, Zr, or Hf;
each X independently is a monoanionic ligand; and
each L independently is a neutral ligand, wherein n is 0, 1 or 2.

2. The composition of claim 1 , wherein:
R 2 , R 3 , R 4 , and R 5 independently are H or a C 1 to C 6 alkyl group;
each R A independently is a C 1 to C 8 hydrocarbyl group;
m is 0, 1, or 2;
L is an ether, a thioether, an amine, a nitrile, or a phosphine; and
n is 0 or 1.

3. The composition of claim 2 , wherein L is diethyl ether and n is 1.

4. The composition of claim 1 , wherein:
R 2 and R 4 independently are a C 1 to C 6 alkyl group, and R 3 and R 5 are H;

M is Zr or Hf;
each X independently is a halide or a C 1 to C 8 hydrocarbyl group; and
L is diethyl ether, tetrahydrofuran, acetonitrile, pyridine, dimethyl amine, diethyl amine, trimethyl amine, trimethylphosphine, or triphenylphosphine.

5. The composition of claim 4 , wherein M is Zr and each X is a benzyl group.

6. The composition of claim 1 , wherein:
the catalyst composition comprises an organoaluminum co-catalyst;
the weight ratio of the organoaluminum co-catalyst to the activator-support is in a range from about 10:1 to about 1:1000; and
the weight ratio of transition metal bis(phenolate) compound to the activator-support is in a range from about 1:20 to about 1:1000.

7. The composition of claim 1 , wherein a catalyst activity of the catalyst composition is from about 20 to about 500 kg of ethylene polymer per gram of transition metal bis(phenolate) compound per hour, under slurry polymerization conditions, with a triisobutylaluminum co-catalyst, using isobutane as a diluent, and with a polymerization temperature of 90° C. and a reactor pressure of 420 psig.

8. The composition of claim 1 , wherein the activator-support comprises a fluorided solid oxide.

9. The composition of claim 1 , wherein the activator-support comprises a sulfated solid oxide.

10. A polymerization process, the process comprising:
contacting the catalyst composition of claim 1 with an olefin monomer and an optional olefin comonomer in a polymerization reactor system under polymerization conditions to produce an olefin polymer.

11. The process of claim 10 , wherein:
the catalyst composition comprises an organoaluminum co-catalyst;
the activator-support comprises a fluorided solid oxide and/or a sulfated solid oxide;
the polymerization reactor system comprises a slurry reactor, a gas-phase reactor, a solution reactor, or a combination thereof; and
the olefin monomer comprises ethylene, and the olefin comonomer comprises 1-butene, 1-hexene, 1-octene, or a mixture thereof.

12. The process of claim 11 , wherein the activator-support comprises fluorided alumina, fluorided silica-alumina, fluorided silica-coated alumina, sulfated alumina, sulfated silica-alumina, sulfated silica-coated alumina, or any combination thereof.

13. The process of claim 11 , wherein:
R 2 , R 3 , R 4 , and R 5 independently are H or a C 1 to C 6 alkyl group;
each R A independently is a C 1 to C 8 hydrocarbyl group;
m is 0, 1, or 2;
L is an ether, a thioether, an amine, a nitrile, or a phosphine; and
n is 0 or 1.

14. The process of claim 11 , wherein:
R 2 and R 4 independently are a C 1 to C 6 alkyl group, and R 3 and R 5 are H;

M is Zr or Hf;
each X independently is a halide or a C 1 to C 8 hydrocarbyl group; and
L is diethyl ether, tetrahydrofuran, acetonitrile, pyridine, dimethyl amine, diethyl amine, trimethyl amine, trimethylphosphine, or triphenylphosphine.

15. The process of claim 14 , wherein M is Zr and each X is a benzyl group.

16. The process of claim 10 , wherein:
the activator-support comprises a fluorided solid oxide; and
the olefin polymer is an ethylene polymer characterized by a ratio of Mw/Mn in a range from about 1.5 to about 5, and a Mw in a range from about 1,500,000 to about 5,000,000 g/mol.

17. The process of claim 16 , wherein the ethylene polymer is an ethylene homopolymer, an ethylene/1-butene copolymer, an ethylene/1-hexene copolymer, or an ethylene/1-octene copolymer.

18. The process of claim 10 , wherein:
the activator-support comprises a sulfated solid oxide; and
the olefin polymer is an ethylene polymer characterized by a ratio of Mw/Mn in a range from 10 to about 200, and a Mw in a range from about 100,000 to about 800,000 g/mol.

19. The process of claim 18 , wherein the ethylene polymer is an ethylene homopolymer, an ethylene/1-butene copolymer, an ethylene/1-hexene copolymer, or an ethylene/1-octene copolymer.

Assignees

• Chevron Phillips Chemical Co Lp
• Chevron Philips Chemical Company Lp

Inventors

• Hlavinka Mark L

Classifications

• C08F110/02 Primary

  Ethene · CPC title

• C07D213/127

  Preparation from compounds containing pyridine rings · CPC title

• C08F4/60158

  ONO · CPC title

• C07F7/00

  Compounds containing elements of Groups 4 or 14 of the Periodic Table · CPC title

• C08F4/64158

  ONO · CPC title