IP Library Granted Patent US 7,018,949
Granted Patent B2
US 7,018,949 · App. 10/748,216 · Granted Mar 28, 2006

Substituted pyridyl amine catalysts and processes for polymerizing and polymers

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Quick Facts
Patent No.
US 7,018,949
App. No.
10/748,216
Granted
Mar 28, 2006
Kind
B2
Abstract

New ligands, compositions, metal-ligand complexes and arrays with pyridyl-amine 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 (29)

1. A catalyst for the production of a polymer comprising a composition comprising:

(1) a ligand characterized by the following general formula:

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

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

R 4 , R 5 , R 6 and R 7 are each independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted heterocycloalkyl, 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;

provided that either R 3 or R 7 is selected only from the group consisting of aryl, substituted aryl, heteroaryl and substituted heteroaryl;

(2) a metal precursor compound characterized by the general formula Hf(L) n wherein each L is independently selected from the group consisting of halide, alkyl, substituted alkyl, 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

(3) optionally, at least one activator.

2. A catalyst for the production of a polymer comprising at least one activator and 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 heterocycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl and combinations thereof;

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

R 4 , R 5 , R 6 and R 7 are each independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, heterocycloalkyl, substituted heterocycloalkyl, 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 4 may be joined together in a ring structure;

provided that either R 3 or R 7 is selected only from the group consisting of aryl, substituted aryl, heteroaryl and substituted heteroaryl;

each L is independently selected from the group consisting of halide, alkyl, substituted alkyl, 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.

3. A catalyst for the production of a polymer comprising at least one activator and 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 heterocycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl and combinations thereof;

T is a bridging group selected 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 heterocycloalkyl, 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 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.

4. The catalyst of either of claims 1 , 2 or 3 , 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 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 heterocycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxyl, aryloxyl, silyl, boryl, phosphino, amino, thio, seleno, halide, nitro, and combinations thereof.

5. The catalyst of either of claims 1 , 2 or 3 , wherein R 3 is selected from the group consisting of benzyl, phenyl, naphthyl, 2-biphenyl, 2-dimethylaminophenyl, 2-methoxyphenyl, anthracenyl, mesityl, 2-pyridyl, 3,5-dimethylphenyl, o-tolyl, and phenanthrenyl.

6. The catalyst of either of claim 4 , wherein Q 1 and Q 5 are, independently, selected from the group consisting of —CH 2 R 15 , —CHR 16 R 17 and methyl, provided that not both Q 1 and Q 5 are methyl, wherein R 15 is selected from the group consisting of alkyl, substituted alkyl, aryl and substituted aryl; R 16 and R 17 are independently selected from the group consisting of alkyl, substituted alkyl, aryl and substituted aryl; and optionally R 16 and R 17 are joined together in a ring structure having from 3-50 non-hydrogen atoms.

7. The catalyst of claim 5 , wherein Q 2 , Q 3 , and Q 4 are each hydrogen and Q 1 and Q 5 are both isopropyl; or both ethyl; or both sec-butyl; or Q 1 is methyl and Q 5 is isopropyl; or Q 1 is ethyl and Q 5 is sec-butyl.

8. The catalyst of claim 4 , wherein R 1 is selected from the group consisting of mesityl; 2-Me-naphthyl; 2,6-(Pr i ) 2 —C 6 H 3 —; 2-Pr-6-Me-C 6 H 3 —; 2,6-Et 2 -C 6 H 3 —; and 2-sec-butyl-6-Et-C 6 H 3 —.

9. The catalyst of either of claims 1 , 2 or 3 , wherein R 7 is selected from the group consisting of phenyl, napthyl, mesityl, anthracenyl and phenanthrenyl.

Assignments (3)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 15, 2004
From: LECLERC, MARGARETE K.; DIAMOND, GARY M.; LAPOINTE, ANNE M.; BOUSSIE, THOMAS R.; MURPHY, VINCE
To: SYMYX TECHNOLOGIES, INC.
Reel/Frame 014852/0809 →