AU2001269725A1 - Polymerization of olefins - Google Patents
Polymerization of olefinsInfo
- Publication number
- AU2001269725A1 AU2001269725A1 AU2001269725A AU6972501A AU2001269725A1 AU 2001269725 A1 AU2001269725 A1 AU 2001269725A1 AU 2001269725 A AU2001269725 A AU 2001269725A AU 6972501 A AU6972501 A AU 6972501A AU 2001269725 A1 AU2001269725 A1 AU 2001269725A1
- Authority
- AU
- Australia
- Prior art keywords
- transition metal
- hydrocarbyl
- ligand
- olefin
- metal complex
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/06—Metallic compounds other than hydrides and other than metallo-organic compounds; Boron halide or aluminium halide complexes with organic compounds containing oxygen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/04—Nickel compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
- C07F7/003—Compounds containing elements of Groups 4 or 14 of the Periodic System without C-Metal linkages
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/02—Ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/02—Ethene
Claims (20)
1. A transition metal complex of a ligand of the formula (I)
wherein:
Y is oxo, NR12 or PR12
Z is O, NR13, S or PR13; each of R1, R2 and R3 is independently hydrogen, hydro- carbyl , substituted hydrocarbyl or a functional group; n is 0 or 1; each R12 is independently hydrogen, hydrocarbyl, substituted hydrocarbyl or a functional group; each R13 is independently hydrogen, hydrocarbyl, substi- tuted hydrocarbyl or a functional group; and provided that any two of R1, R2 and R3 geminal or vicinal to one another taken together may form a ring.
2. The transition metal complex of claim 1, character- ized in that the transition metal is a Group 3-11 transition metal .
3. The transition metal complex of claim 2, characterized in that the transition metal is selected from the group consisting of Ni, Zr, Ti , Fe, Co and Cu.
4. The transition metal complex of claim 1, characterized in that Z is O or NR13, and n is 0.
53
5. The transition metal complex of claim 1, characterized in that:
Y is oxo; Z is NR13; R1 is hydrogen or hydrocarbyl; n is 0; and R13 is hydrocarbyl or substituted hydrocarbyl having an Es of less than -1.0 or aryl or substituted aryl in which at least one bond vicinal to the free bond of the aromatic group is substituted; or
Y is NR12; Z is NR13; n is 0; R1 is hydrogen or hydrocarbyl; R12 and R13 are each independently hydrocarbyl or substi- tuted hydrocarbyl, one or both having an Es of less than
-1.0, or aryl or substituted aryl in which at least one bond vicinal to the free bond of the aromatic group is substituted.
6. The transition metal complex of claim 1, characterized in that it has the formula (L1) x (L2) y (L3) ZM (VIII), wherein L3 is (I); z is 1 or 2; M is a transition metal of oxidation state q; y is an integer of 1 to 3; x=(q-z); each L1 is independently a monodentate, monoanionic ligand, wherein at least one L1 group is a ligand that may add to an olefin; and L2 is a monodentate neutral ligand which may be displaced by an olefin, or an empty coordination site; or L1 and L2 taken together are a monoanionic, bidentate ligand into which an olefin molecule may insert between the ligand and M.
7. The transition metal complex of claim 1, characterized in that it has the formula (III), (IV), (V) or (VI):
54
wherein M is the transition metal; each L1 is independently a monodentate, monoanionic ligand, wherein at least one L1 group is a ligand that may add to an olefin; and L2 is a monodentate neutral ligand which may be displaced by an olefin, or an empty coordination site; or L1 and L2 taken together are a monoanionic, bidentate ligand into which an olefin molecule may insert between the ligand and M.
8. A process for the polymerization of olefins, comprising the step of contacting, under olefin polymerizing conditions : a monomer component comprising one or more of olefins of the formula H2C=CHR4, a norbornene, a styrene, a cyclopen-
55 tene or a polar olefin, especially an olefin of the formula H2C=CHR4 and/or a polar olefin of the formula H2C=CHR5C02R6 , wherein R4 is hydrogen, alkyl or substituted alkyl, R5 is a covalent bond, alkylene or substituted alkylene, and R6 is hydrogen, a metal cation, hydrocarbyl or substituted hydrocarbyl, with a transition metal polymerization catalyst, characterized in that the transition metal polymerization catalyst comprises a transition metal complex as set forth in any one of claims 1-7.
9. The process of claim 8, characterized in that a cocatalyst is present.
10. The process of claim 8, characterized in that the monomer component comprises ethylene.
11. A process for the manufacture of a polar copolymer, wherein one or more hydrocarbon olefins, one or more polar olefins, and a polymerization catalyst system having a transition metal complex component containing a transition metal of groups 6-11 or a lanthanide metal, are contacted under polymerizing conditions to form said polar copolymer, characterized in that the transition metal complex component comprises a Zwitterionic complex.
12. The process of claim 11, characterized in that said transition metal is from Groups 8-11.
13. The process of claim 12, characterized in that said transition metal is Pd, Ni or Cu.
56
14. The process of claim 13, characterized in that said transition metal is Ni .
15. The process of claim 11, characterized in that said Zwitterionic complex is a Lewis acid adduct of a transition metal complex, the transition metal complex comprising a transition metal complexed to a ligand, wherein a Lewis base is present in the ligand, and wherein the Lewis acid is coordinated to the Lewis base.
16. The process of claim 15, characterized in that the transition metal complex is as set forth in any one of claims 1-7.
17. The process of claim 11, characterized in that said Zwitterionic complex is a Lewis acid adduct of a transition metal complex, wherein said Lewis acid is a borane or an aluminane .
18. The process of claim 17, characterized in that said Lewis acid is a tris (pentafluorophenyl) borane, triphenylbo- rane or a trihydrocarbylaluminum.
19. The process of any one of claims 11-18, character- ized in that said hydrocarbon olefin is ethylene, and said polar olefin is one or more of H2C=CHR5C02R6, wherein R5 is n- alkylene or a covalent bond, and R6 is hydrocarbyl or substituted hydrocarbyl .
20. The process of claim 19, characterized in that an ethylene pressure is about 700 kPa or more, and said process is run at about 50°C to about 170°C.
57
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US20808700P | 2000-05-31 | 2000-05-31 | |
US60/208,087 | 2000-05-31 | ||
US21160100P | 2000-06-15 | 2000-06-15 | |
US60/211,061 | 2000-06-15 | ||
US21403600P | 2000-06-23 | 2000-06-23 | |
US60/214,036 | 2000-06-23 | ||
PCT/US2001/017636 WO2001092348A2 (en) | 2000-05-31 | 2001-05-31 | Polymerization of olefins |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2001269725A1 true AU2001269725A1 (en) | 2001-12-11 |
Family
ID=27395149
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2001269725A Abandoned AU2001269725A1 (en) | 2000-05-31 | 2001-05-31 | Polymerization of olefins |
Country Status (10)
Country | Link |
---|---|
US (3) | US6506861B2 (en) |
EP (1) | EP1290043A2 (en) |
JP (1) | JP2003535107A (en) |
KR (1) | KR20030005432A (en) |
CN (1) | CN100406478C (en) |
AU (1) | AU2001269725A1 (en) |
BR (1) | BR0111338A (en) |
CA (1) | CA2408663A1 (en) |
MX (1) | MXPA02011811A (en) |
WO (1) | WO2001092348A2 (en) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6245871B1 (en) * | 1997-04-18 | 2001-06-12 | Eastman Chemical Company | Group 8-10 transition metal olefin polymerization catalysts |
SG96633A1 (en) * | 2000-07-04 | 2003-06-16 | Mitsui Chemicals Inc | Process for producing polar olefin copolymer and polar olefin copolymer obtained thereby |
US20030130452A1 (en) * | 2001-10-12 | 2003-07-10 | Johnson Lynda Kaye | Copolymers of ethylene with various norbornene derivatives |
US7030200B2 (en) * | 2002-03-06 | 2006-04-18 | E.I. Du Pont De Nemours And Company | Catalysts for olefin polymerization |
US7037990B2 (en) * | 2003-01-03 | 2006-05-02 | Nippon Synthetic Chemical Company | Transition metal complexes in the controlled synthesis of polyolefins substituted with functional groups |
DE10304158A1 (en) * | 2003-02-03 | 2004-08-05 | Bayer Ag | New transition metal complexes with azo ligands, useful as catalysts, particularly for polymerization of olefins, especially in presence of polar additives |
US7754839B2 (en) * | 2003-03-03 | 2010-07-13 | The Regents Of The University Of California | Quasi-living metal catalyst for ethylene homo-polymerization and co-polymerization with 5-norbornen -2-yl acetate |
US7825200B2 (en) * | 2003-02-28 | 2010-11-02 | The Regents Of The University Of California | Controlled free radical grafting from polyolefins |
US7968487B2 (en) | 2003-02-28 | 2011-06-28 | The Regents Of The University Of California | Single component, phosphine-free, initiators for ethylene homopolymerization and copolymerization with functionalized co-monomers |
US7259214B2 (en) * | 2003-02-28 | 2007-08-21 | The Regents Of The University Of California | Metal catalyst for olefin polymerization and co-polymerization with functional monomers |
DE10310289A1 (en) * | 2003-03-10 | 2004-09-23 | Bayer Ag | Process for the preparation of an azo catalyst for the polymerization of olefins |
US7087687B2 (en) * | 2003-08-21 | 2006-08-08 | Rohm And Haas Company | Catalytic composition and its preparation and use for preparing polymers from ethylenically unsaturated monomers |
US7005489B2 (en) * | 2003-09-29 | 2006-02-28 | Equistar Chemicals, Lp | Zwitterionic Metallocycles |
US6903169B1 (en) * | 2003-12-30 | 2005-06-07 | Equistar Chemicals, Lp | LTMC polymerization of unsaturated monomers |
US7199074B2 (en) * | 2004-06-14 | 2007-04-03 | Rohm And Haas Company | Catalytic composition and its preparation and use for preparing polymers from ethylenically unsaturated monomers |
US7172986B2 (en) * | 2004-06-14 | 2007-02-06 | Rohm And Haas Company | Catalytic composition and its preparation and use for preparing polymers from ethylenically unsaturated monomers |
US7635739B2 (en) * | 2005-08-31 | 2009-12-22 | Rohm And Haas Company | Substantially linear polymers and methods of making and using same |
FR2937643B1 (en) | 2008-10-27 | 2011-10-14 | Arkema France | NOVEL BLOCK COPOLYMERS OF POLAR AND APOLAR OLEFINS |
US20110065950A1 (en) * | 2009-09-03 | 2011-03-17 | Technical University Of Denmark | Palladium catalyst system comprising zwitterion and/or acid-functionalyzed ionic liquid |
WO2011026860A1 (en) | 2009-09-03 | 2011-03-10 | Technical Univeristy Of Denmark | Palladium catalyst system comprising zwitterion and/or acid-functionalized ionic liquid |
IT201700006307A1 (en) * | 2017-01-20 | 2018-07-20 | Versalis Spa | BONE-AZOTATE COMPLEX OF IRON, CATALYTIC SYSTEM INCLUDING THE BONE-AZOTATE COMPLEX OF IRON AND PROCEDURE FOR (CO) POLYMERIZATION OF CONJUGATED DIENES |
CN109694436A (en) * | 2017-10-24 | 2019-04-30 | 中国石油化工股份有限公司 | A kind of alkene-alkene alkoxide polymer and preparation method thereof |
CN109096139B (en) * | 2018-09-03 | 2021-03-02 | 贵州大学 | Preparation method of alpha-carbonyl amide derivative |
CN112759710B (en) * | 2021-01-22 | 2023-09-08 | 吴军化 | Para-phenoxy substituted alpha-diimine iron catalyst and preparation method thereof |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE188967T1 (en) * | 1994-06-13 | 2000-02-15 | Targor Gmbh | TRANSITION METAL JOINTS |
US5486632A (en) * | 1994-06-28 | 1996-01-23 | The Dow Chemical Company | Group 4 metal diene complexes and addition polymerization catalysts therefrom |
US5972822A (en) * | 1994-08-02 | 1999-10-26 | The Dow Chemical Company | Biscyclopentadienyldiene complex containing addition polymerization catalysts |
US5942461A (en) * | 1995-11-06 | 1999-08-24 | Minnesota Mining And Manufacturing Company | Polymerizable compositions comprising alpha-olefin hydrocarbon monomers and methods of use therefor |
US6174974B1 (en) * | 1996-07-05 | 2001-01-16 | Bayer Aktiengesellschaft | Method for producing thermoplastic elastomers |
US5939503A (en) * | 1996-08-09 | 1999-08-17 | California Institute Of Technology | Group IV zwitterion ansa metallocene (ZAM) catalysts for α-olefin polymerization |
US6174975B1 (en) | 1998-01-13 | 2001-01-16 | E.I. Du Pont De Nemours And Company | Polymerization of olefins |
EP0952998B1 (en) | 1997-01-14 | 2002-06-19 | E.I. Du Pont De Nemours And Company | Polymerization of ethylene |
WO1998030609A1 (en) * | 1997-01-14 | 1998-07-16 | E.I. Du Pont De Nemours And Company | Polymerization of olefins |
US6103658A (en) * | 1997-03-10 | 2000-08-15 | Eastman Chemical Company | Olefin polymerization catalysts containing group 8-10 transition metals, processes employing such catalysts and polymers obtained therefrom |
US6200925B1 (en) | 1997-03-13 | 2001-03-13 | Eastman Chemical Company | Catalyst compositions for the polymerization of olefins |
US6573345B1 (en) | 1997-03-24 | 2003-06-03 | Cryovac, Inc. | Catalyst compositions and processes for olefin oligomerization and polymerization |
US6410664B1 (en) | 1997-03-24 | 2002-06-25 | Cryovac, Inc. | Catalyst compositions and processes for olefin polymers and copolymers |
US6174976B1 (en) * | 1998-02-24 | 2001-01-16 | Eastman Chemical Company | Neutral nickel complexes for olefin polymerization |
TW562810B (en) * | 1998-04-16 | 2003-11-21 | Mitsui Chemicals Inc | Catalyst for olefinic polymerization and method for polymerizing olefine |
JP3747354B2 (en) * | 1998-08-27 | 2006-02-22 | 三井化学株式会社 | Transition metal compound, catalyst for olefin polymerization, and polymerization method |
US6465385B1 (en) * | 1999-02-12 | 2002-10-15 | Sunoco, Inc. (R&M) | Zwitterionic polymerization catalyst |
AU7507001A (en) * | 2000-05-31 | 2001-12-11 | Du Pont | Catalysts for olefin polymerization |
-
2001
- 2001-05-31 MX MXPA02011811A patent/MXPA02011811A/en unknown
- 2001-05-31 WO PCT/US2001/017636 patent/WO2001092348A2/en active Application Filing
- 2001-05-31 AU AU2001269725A patent/AU2001269725A1/en not_active Abandoned
- 2001-05-31 CA CA002408663A patent/CA2408663A1/en not_active Abandoned
- 2001-05-31 US US09/871,100 patent/US6506861B2/en not_active Expired - Fee Related
- 2001-05-31 CN CNB018105750A patent/CN100406478C/en not_active Expired - Fee Related
- 2001-05-31 JP JP2002500959A patent/JP2003535107A/en active Pending
- 2001-05-31 KR KR1020027016228A patent/KR20030005432A/en not_active Application Discontinuation
- 2001-05-31 BR BR0111338-0A patent/BR0111338A/en not_active Application Discontinuation
- 2001-05-31 EP EP01948254A patent/EP1290043A2/en not_active Withdrawn
-
2002
- 2002-10-17 US US10/272,765 patent/US7683147B2/en not_active Expired - Fee Related
- 2002-10-17 US US10/273,049 patent/US7115763B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
CN1432027A (en) | 2003-07-23 |
KR20030005432A (en) | 2003-01-17 |
EP1290043A2 (en) | 2003-03-12 |
MXPA02011811A (en) | 2003-05-14 |
US20020028741A1 (en) | 2002-03-07 |
BR0111338A (en) | 2003-06-17 |
US20030130453A1 (en) | 2003-07-10 |
CN100406478C (en) | 2008-07-30 |
US7683147B2 (en) | 2010-03-23 |
WO2001092348A3 (en) | 2002-07-25 |
WO2001092348A2 (en) | 2001-12-06 |
US20030130449A1 (en) | 2003-07-10 |
US7115763B2 (en) | 2006-10-03 |
US6506861B2 (en) | 2003-01-14 |
JP2003535107A (en) | 2003-11-25 |
CA2408663A1 (en) | 2001-12-06 |
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