Transition metal complex for use in or as a catalyst for olefin polymerization

Patent metadata

Field	Value
Publication number	US-11312795-B2
Application number	US-201816617702-A
Country	US
Kind code	B2
Filing date	May 18, 2018
Priority date	May 28, 2017
Publication date	Apr 26, 2022
Grant date	Apr 26, 2022

Abstract

A catalyst for olefin polymerization containing at least one metal complex comprising at least one —SF5 group attached to a ligand bound to the metal. The invention further relates to catalyst, a process for making polyolefins and dispersions of UHMWPE.

First claim

The invention claimed is:

1. Transition metal complex suitable for use in a catalyst for olefin polymerization wherein the metal complex comprises at least one —SF 5 group attached to a ligand bound to the metal, wherein the metal is Ti, Zr, or Hf.

2. The transition metal complex according to claim 1 , having one of the structures according to:

3. A catalyst for polymerization of olefins, the catalyst comprising a transition metal complex according to claim 1 and optionally a cocatalyst.

4. A process for the (co)polymerization of olefinic monomers, the process comprising polymerizing one or more olefinic monomers in the presence of a catalyst comprising a transition metal complex according to claim 1 and optionally a cocatalyst, wherein an activator is present and the molar ratio of the activator to the catalyst is in the range from 0.1 to 10.

5. Transition metal complex suitable for use in a catalyst for olefin polymerization wherein the metal complex comprises at least one —SF 5 group attached to a ligand bound to the metal, and wherein the complex is a catalyst or compound having the general structure 12.

where the substituents and indices have the following meanings:
M is a transition metal from groups 3 to 10 of the periodic table of the elements,
L 1 denotes a neutral Lewis base,
L 2 denotes halide ions, amide ions (R 16 ) h NH 2-h , h denoting an integer from 0 to 2, C 1 -C 6 alkyl anions, allyl anions, benzyl anions or aryl anions, wherein optionally L 1 and L 2 are linked by one or more covalent bonds;
X is CR or nitrogen atom (N), wherein R is hydrogen, a C 1 -C 6 alkyl group, a C 7 -C 13 aralkyl radical or a C 6 -C14 aryl group, unsubstituted or substituted by one or more C 1 -C 12 alkyl groups, halogens, mono- or polyhalogenated C 1 -C 12 alkyl groups, C 1 -C 12 alkoxy groups, silyloxy groups OSiR 11 R 12 R 13 ; amino groups NR 14 R 15 or C 1 -C 12 thioether groups;
Y is OH group, oxygen, sulfur, N-R 10 or P-R 10 , provided that when Y is OH group, the bond between Y and M is a coordinate bond;
a is 1 or 2; b=0 or 1; c=0 or 1, and wherein a+b+c equals the valency of the transition metal M and wherein b+c is 1 or 2;
R 1 to R 9 are independently of one another:
hydrogen;
C 1 -C 12 alkyl, the alkyl groups being branched or unbranched, optionally C 1 -C 12 alkyl being substituted one or more times by identical or different substituents selected from C 1 -C 12 alkyl groups, halogens, C 1 -C 12 alkoxy groups, C 1 -C 12 thioether groups; and C 7 -C 13 aralkyl;
C 3 -C 12 cycloalkyl;
C 3 -C 12 cycloalkyl substituted one or more times by identical or different substituents selected from C 1 -C 12 alkyl groups, halogens, C 1 -C 12 alkoxy groups and C 1 -C 12 thioether groups;
C 6 -C 14 aryl, optionally substituted by identical or different substituents selected from one or more C 1 -C 12 alkyl groups, halogens, mono- or polyhalogenated C 1 -C 12 alkyl groups, C 1 -C 12 alkoxy groups, silyloxy groups OSiR 11 R 12 R 13 ; amino groups NR 14 R 15 and C 1 -C 12 thioether groups;
C 1 -C 12 alkoxy groups;
silyloxy groups OSiR 11 R 12 R 13 ;
halogens;
NO 2 groups or amino groups NR 14 R 15 ; or
—SF 5 groups or radicals of the formula 14 below, where n is an integer from 1 to 5;
optionally in each case two adjacent radicals R 1 to R 9 forming with one another a saturated or unsaturated 5- to 8-membered ring;

R 10 to R 16 independently of one another being hydrogen, C 1 -C 20 alkyl groups, which are optionally substituted with O(C 1 -C 6 alkyl) or N(C 1 -C 6 alkyl) 2 groups, C 3 -C 12 cycloalkyl groups, C 7 -C 13 aralkyl radicals, C 7 -C 13 substituted aralkyl radicals, C 6 -C 14 aryl groups or substituted C 6 -C 14 aryl groups;

wherein at least one of the radicals R 1 to R 9 is in the form of a —SF 5 group or a radical of the formula 14 below

where n is an integer from 1 to 5.

6. A catalyst for olefin polymerization, the catalyst comprising at least one transition metal complex according to claim 5 .

7. The transition metal complex according to claim 5 , wherein the metal M is a transition metal from groups 3-6 of the period table, a is 2, indicating that the transition metal comprises 2 ligands.

8. The transition metal complex according to claim 5 , wherein the complex has a structure according to formula 13,

and wherein R 1 -R 9 , L 1 , L 2 , M, X, and Y have the meanings as defined in claim 5 .

9. The transition metal complex according to claim 5 , wherein Y is an —OH group or oxygen.

10. The transition metal complex according to claim 8 , wherein the complex has a structure represented by formula 15

wherein R 5 , R 7 , and R 9 are independently H, methyl, isopropyl, NO 2 or

wherein R 1 and R 3 are independently H, methyl, isopropyl, NO 2 , I, or

where n is an integer from 1 to 5;
with the proviso that at least one of R 1 , R 3 , R 5 , R 7 and R 9 is a

wherein n is an integer from 1 to 5.

11. The transition metal complex according to claim 5 , wherein the —SF 5 containing group is a 3,5-dipentafluorosulfanyl phenyl group.

12. The transition metal complex according to claim 8 , wherein the complex has a structure represented by any one of formula 13 1 -13 5 ,

wherein in formula 13 3 and 13 4 , R 5 and R 9 are independently H, —CH 3 or iso-propyl, and

wherein in formula 13 1 and formula 13 5 , R 1 and R 3 are independently H, CH 3 ,
isopropyl, phenyl, naphthyl, anthracenyl, —NO 2 , or

wherein in formula 13 1 -13 5 , L 1 is pyridine or 3,3′,3″-phosphanetriyl tris(benzenesulfonic acid) trisodium salt and L 2 is a methyl group.

13. The transition metal complex according to claim 5 , wherein L 1 is pyridine or 3,3′,3″-phosphanetriyl tris(benzenesulfonic acid) trisodium salt, L 2 is a methyl group, R 1 and R 3 are independently H, CH 3 , isopropyl, phenyl, naphthyl, anthracenyl, NO 2 , or

14. The transition metal complex according to claim 5 , wherein L 1 denotes phosphanes (R 19 ) x PH 3-x or amines (R 16 ) x NH 3-x with identical or different radicals R 16 , ethers (R 16 ) 2 O, H 2 O, alcohols (R 16 )OH, pyridine, pyridine derivatives of the formula C 5 H 5-x (R 16 ) x N, CO, C 1 -C 12 alkylnitriles, C 6 -C 14 arylnitriles or ethylenically unsaturated double bond systems, and wherein x denotes an integer fr

Assignees

• Sabic Global Technologies Bv

Inventors

• Friederichs Nicolaas Hendrika
• Zuideveld Martin Alexander
• Kenyon Philip
• Mecking Stefan

Classifications

• C08F210/02

  Ethene · CPC title

• C08F4/619

  Component covered by group C08F4/60 containing a transition metal-carbon bond {(C08F4/60003 - C08F4/60196 take precedence)} · CPC title

• C08F4/64048

  NO · CPC title

• C08F4/64051 Primary

  NS · CPC title

• C08F110/02 Primary

  Ethene · CPC title