IP Library Granted Patent US 6,900,321
Granted Patent B2
US 6,900,321 · App. 09/992,630 · Granted May 31, 2005

Substituted pyridyl amine complexes, and catalysts

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Quick Facts
Patent No.
US 6,900,321
App. No.
09/992,630
Granted
May 31, 2005
Kind
B2
Abstract

New ligands, compositions, metal-ligand complexes and arrays with pyridylamine ligands are disclosed that catalyze the polymerization of monomers into polymers. Certain of these catalysts with hafnium metal centers have high performance characteristics, including higher comonomer incorporation into ethylene/olefin copolymers, where such olefins are for example, 1-octene, isobutylene or styrene. Certain of the catalysts are particularly effective at polymerizing propylene to high molecular weight isotactic polypropylene in a solution process at a variety of polymerization conditions.

Claims (39)

1. A metal-ligand complex characterized by the following formula:

wherein R 1 is selected from the group consisting of alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl and combinations thereof;

T is a bridging group selected from the group consisting of —CR 2 R 3 — and —SiR 2 R 3 — with R 2 and R 3 independently selected from the group from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxyl, aryloxyl, silyl, boryl, phosphino, amino, thio, seleno, halide, nitro, and combinations thereof;

J″ is selected from the group consisting of heteroaryl and substituted heteroaryl;

each L is independently selected from the group consisting of halide, alkyl, substituted alky, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl heterocycloalkyl, substituted heterocycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, aryloxy, hydroxy, boryl, silyl, amino, amine, hydrido, allyl, diene, seleno, phosphino, phosphine, carboxylates, thio, 1,3-dionates, oxalates, carbonates, nitrates, sulphates, ethers, thioethers and combinations thereof or optionally two or more L groups are joined into a ring structure; n is 1, 2, 3, 4, 5, or 6; and x is 1 or 2.

2. The metal complex of claim 1 having the formula:

wherein each of R 4 , R 5 , R 6 and R 7 is independently selected from the group consisting of hydrogen, alky, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aiyl, heteroaryl, substituted heteroaryl, alkoxyl, aryloxyl, silyl, boryl, phosphino, amino, thio, seleno, halide, nitro, and combinations thereof; and optionally, any combination of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 or R 7 may be joined together in a ring structure.

3. The metal complex of claim 2 , wherein said complex is characterized by the formula:

wherein Q 1 , Q 2 , Q 3 Q 4 and Q 5 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxyl, aryloxyl, silyl, boryl, phosphino, amino, thio, seleno, nitro, and combinations thereof; optionally any 2 of Q 1 , Q 2 , Q 3 Q 4 and Q 5 are joined together in a ring structure; and x=1.

4. The metal complex of claim 2 , wherein said complex is characterized by the formula:

such that T is —CR 2 , R 3 — and wherein R 10 , R 11 , R 12 and R 13 are each independently selected from the group consisting of hydrogen, halide, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, aryloxy, silyl, boryl, phosphino, amino, thio, seleno, nitro, and combinations thereof; optionally, two or more R 10 , R 11 , R 12 and R 13 groups may be joined to form a fused ring system having from 3-50 non-hydrogen atoms; and

R 14 is selected from the group consisting of hydrogen, alkyl, substituted alky, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, aryloxy, silyl, boryl, phosphino, amino, thio, seleno, halide, nitro, and combinations thereof; and x=1.

5. The metal complex of claim 4 , wherein said complex is characterized by the general formula:

wherein Q 1 , Q 2 , Q 3 Q 4 and Q 5 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxyl, aryloxyl, silyl, boryl, phosphino, amino, thio, seleno, nitro, and combinations thereof; optionally any 2 of Q 1 , Q 2 , Q 3 Q 4 and Q 5 are joined together in a ring structure.

6. A metal complex characterized by the formula:

where M is zirconium or hafnium;

wherein R 1 is selected from the group consisting of alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl and combinations thereof;

T is a bridging group selected from the group consisting of —CR 2 R 3 — and —SiR 2 R 3 — with R 2 and R 3 being independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxyl, aryloxyl, silyl, boryl, phosphino, amino, thio, seleno, halide, nitro, and combinations thereof;

J′″ being selected from the group of substituted heteroaryls with 2 atoms bonded to the metal M, at least one of those 2 atoms being a heteroatom, and with one atom of J′″ is bonded to M via a dative bond, the other through a covalent bond; and

L 1 and L 2 are independently selected from the group consisting of halide, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted beteroalkyl, heterocycloalkyl, substituted heterocycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, aryloxy, hydroxy, boryl, silyl, amino, amine, hydrido, allyl, diene, seleno, phosphino, phosphine, carboxylates, thio, 1,3-dionates, oxalates, carbonates, nitrates, sulphates, ethers, thioethers and combinations thereof or optionally the two L groups are joined into a ring structure.

7. The complex of claim 6 , wherein said complex is characterized by the formula:

wherein each of R 4 , R 5 and R 6 is independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxyl, aryloxyl, silyl, boryl, phosphino, amino, thio, seleno, halide, nitro, and combinations thereof; and optionally, any combination of R 1 , R 2 , R 3 , R 4 , R 5 , or R 6 may be joined together in a ring structure; and

E″ is either carbon or nitrogen and is part of a cyclic aryl, substituted aryl, heteroaryl, or substituted heteroaryl group.

8. The metal complex of claim 7 , wherein said complex is characterized by the formula:

wherein R 10 , R 11 , R 12 and R 13 are each independently selected from the group consisting of hydrogen, halide, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, aryloxy, silyl, boryl, phosphino, amino, thio, seleno, nitro, and combinations thereof; optionally, two or more R 10 , R 11 , R 12 and R 13 groups may be joined to form a fused ring system having from 3-50 non-hydrogen atoms.

9. The metal complex of claim 8 , wherein said complex is characterized by the formula:

wherein Q 1 , Q 2 , Q 3 Q 4 and Q 5 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxyl, aryloxyl, silyl, boryl, phosphino, amino, thio, seleno, nitro, and combinations thereof; or optionally, two of Q 2 , Q 3 and Q 4 are joined together in a ring structure.

10. The complex of either of claim 1 , 2 , 4 , 6 , 7 or 8 , wherein R 1 is characterized by the general formula:

wherein E is either carbon or nitrogen,

Q 1 and Q 5 are substituents on the R 1 ring at a position ortho to E, with at least one of Q 1 or Q 5 being bulky, wherein Q 1 and Q 5 are independently selected from the group consisting of alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl and silyl, but provided that Q 1 and Q 5 are not both methyl; and

Q″ q represents additional possible substituents on the ring, with q being 1, 2, 3, 4 or 5 and Q″ being selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxyl, aryloxyl, silyl, boryl, phosphino, amino, thio, seleno, halide, nitro, and combinations thereof.

11. The complex of claim 10 , wherein R 1 is characterized by the general formula

wherein Q 2 and Q 3 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted hetercycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxyl, aryloxyl, silyl, boryl, phosphino, amino, thio, seleno, nitro, and combinations thereof; or optionally, Q 2 and Q 3 are joined together in a ring structure.

12. The complex of either of claim 6 , 7 , 8 or 9 , wherein M is hafnium.

13. The complex of either of claim 6 , 7 , 8 or 9 , wherein L 1 and L 2 are the same and selected from the group consisting of methyl and dimethylamino.

14. The complex of claim 13 , wherein said complex is selected from the group consisting of:

15. A catalyst comprising the complex of either of claim 1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 or 9 , combined with an activator, combination of activators or activating technique.

16. The catalyst of claim 15 , wherein said catalyst comprises an activator that is an ionic activator.

17. The catalyst of claim 16 , additionally comprising at least one of a group 13 reagent, a divalent metal reagent or an alkali metal reagent.

Assignments (2)
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 →