ATE251945T1 - Hydrocarbylphosphinimin/cyclopentadienyl-komple e von metallen der gruppe 4 und deren verwendung zur olefinpolymerisation - Google Patents
Hydrocarbylphosphinimin/cyclopentadienyl-komple e von metallen der gruppe 4 und deren verwendung zur olefinpolymerisationInfo
- Publication number
- ATE251945T1 ATE251945T1 AT00954231T AT00954231T ATE251945T1 AT E251945 T1 ATE251945 T1 AT E251945T1 AT 00954231 T AT00954231 T AT 00954231T AT 00954231 T AT00954231 T AT 00954231T AT E251945 T1 ATE251945 T1 AT E251945T1
- Authority
- AT
- Austria
- Prior art keywords
- complexes
- cyclopentadienyl
- hydrocarbylphosphiniminine
- comple
- metals
- Prior art date
Links
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 title abstract 2
- HPYIUKIBUJFXII-UHFFFAOYSA-N Cyclopentadienyl radical Chemical compound [CH]1C=CC=C1 HPYIUKIBUJFXII-UHFFFAOYSA-N 0.000 title 1
- 150000001336 alkenes Chemical class 0.000 title 1
- 229910052751 metal Inorganic materials 0.000 title 1
- 239000002184 metal Substances 0.000 title 1
- 150000002739 metals Chemical class 0.000 title 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title 1
- 238000006116 polymerization reaction Methods 0.000 title 1
- 238000005481 NMR spectroscopy Methods 0.000 abstract 2
- 239000003446 ligand Substances 0.000 abstract 2
- 239000013078 crystal Substances 0.000 abstract 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 abstract 1
- QLNAVQRIWDRPHA-UHFFFAOYSA-N iminophosphane Chemical compound P=N QLNAVQRIWDRPHA-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002524 organometallic group Chemical group 0.000 abstract 1
- 239000002685 polymerization catalyst Substances 0.000 abstract 1
- 238000002424 x-ray crystallography Methods 0.000 abstract 1
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
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1845—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
- B01J31/1875—Phosphinites (R2P(OR), their isomeric phosphine oxides (R3P=O) and RO-substitution derivatives thereof)
- B01J31/188—Amide derivatives thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/22—Organic complexes
- B01J31/2282—Unsaturated compounds used as ligands
- B01J31/2295—Cyclic compounds, e.g. cyclopentadienyls
-
- 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
- C07F17/00—Metallocenes
-
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/40—Complexes comprising metals of Group IV (IVA or IVB) as the central metal
- B01J2531/46—Titanium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
- B01J31/38—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of titanium, zirconium or hafnium
-
- 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
- C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
-
- 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
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65908—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an ionising compound other than alumoxane, e.g. (C6F5)4B-X+
-
- 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
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65912—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an organoaluminium compound
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/943—Polymerization with metallocene catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002282070A CA2282070C (en) | 1999-09-10 | 1999-09-10 | Hydrocarbyl phosphinimine/cyclopentadienyl complexes of group iv metals and preparation thereof |
| PCT/CA2000/000978 WO2001019512A1 (en) | 1999-09-10 | 2000-08-24 | Hydrocarbyl phosphinimine/cyclopentadienyl complexes of group 4 and their use in olefin polymerization |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE251945T1 true ATE251945T1 (de) | 2003-11-15 |
Family
ID=4164113
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT00954231T ATE251945T1 (de) | 1999-09-10 | 2000-08-24 | Hydrocarbylphosphinimin/cyclopentadienyl-komple e von metallen der gruppe 4 und deren verwendung zur olefinpolymerisation |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6440890B1 (de) |
| EP (1) | EP1214146B1 (de) |
| JP (1) | JP4619599B2 (de) |
| KR (1) | KR100670424B1 (de) |
| AT (1) | ATE251945T1 (de) |
| AU (1) | AU6678300A (de) |
| BR (1) | BR0013870B1 (de) |
| CA (1) | CA2282070C (de) |
| DE (1) | DE60005982T2 (de) |
| ES (1) | ES2208398T3 (de) |
| WO (1) | WO2001019512A1 (de) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2347410C (en) * | 2001-05-11 | 2009-09-08 | Nova Chemicals Corporation | Solution polymerization process catalyzed by a phosphinimine catalyst |
| US7309741B2 (en) * | 2004-06-01 | 2007-12-18 | Nova Chemicals (International) S.A. | Polyolefin blends and pipe |
| EP1801113A1 (de) * | 2005-12-22 | 2007-06-27 | DSM IP Assets B.V. | Zwitterionischer Phosphinimin-Katalysator |
| DE102007057854A1 (de) * | 2007-11-28 | 2009-06-04 | Philipps-Universität Marburg | Cyclopentadienylphosphazen-Komplexe (CpPN-Komplexe) von Metallen der 3. und 4. Gruppe und der Lanthanoide |
| US9120984B2 (en) | 2012-12-21 | 2015-09-01 | Governors Of The University Of Alberta | Transition metal catalysts for hydrodesulfurization |
| US9051229B2 (en) | 2012-12-21 | 2015-06-09 | Governors Of The University Of Alberta | Transition metal catalysts for C—O hydrogenolysis and hydrodeoxygenation |
| US9120741B2 (en) | 2012-12-21 | 2015-09-01 | Governors Of The University Of Alberta | Transition metal catalysts for hydrogenation and hydrosilylation |
| US8901334B2 (en) | 2012-12-21 | 2014-12-02 | Governors Of The University Of Alberta | Transition metal-phosphoranimide catalysts |
| US9458395B2 (en) | 2013-05-21 | 2016-10-04 | Governors Of The University Of Alberta | Catalysts for hydrodesulfurization |
| US9000198B2 (en) | 2013-05-21 | 2015-04-07 | Governors Of The University Of Alberta | Mixed-valent transition metal-phosphoranimide catalysts |
| US9441063B2 (en) | 2014-10-09 | 2016-09-13 | Chevron Phillips Chemical Company Lp | Titanium phosphinimide and titanium iminoimidazolidide catalyst systems with activator-supports |
| KR101919435B1 (ko) * | 2015-10-21 | 2018-11-16 | 주식회사 엘지화학 | 전이금속 화합물, 이를 포함하는 촉매 조성물 및 이를 이용한 폴리올레핀의 제조 방법 |
| US10005865B1 (en) | 2017-04-07 | 2018-06-26 | Chevron Phillips Chemical Company Lp | Methods for controlling molecular weight and molecular weight distribution |
| US10428091B2 (en) | 2017-04-07 | 2019-10-01 | Chevron Phillips Chemical Company Lp | Catalyst systems containing low valent titanium-aluminum complexes and polymers produced therefrom |
| US10000595B1 (en) | 2017-04-07 | 2018-06-19 | Chevron Phillips Chemical Company Lp | Catalyst systems containing low valent titanium compounds and polymers produced therefrom |
| JP7767014B2 (ja) * | 2020-01-22 | 2025-11-11 | 三井化学株式会社 | 遷移金属化合物、オレフィン重合用触媒、およびオレフィン重合体の製造方法 |
| JP7839869B2 (ja) * | 2022-03-31 | 2026-04-02 | ポリプラスチックス株式会社 | 触媒組成物の保管方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3566819B2 (ja) * | 1996-10-04 | 2004-09-15 | 関東化学株式会社 | 新規な有機遷移金属化合物 |
| CA2206944C (en) * | 1997-05-30 | 2006-08-29 | Douglas W. Stephan | High temperature solution polymerization process |
| CA2210131C (en) * | 1997-07-09 | 2005-08-02 | Douglas W. Stephan | Supported phosphinimine-cp catalysts |
| US5986120A (en) * | 1998-02-10 | 1999-11-16 | The Research Foundation Of The State University Of New York | Metal triflimide complexes |
-
1999
- 1999-09-10 CA CA002282070A patent/CA2282070C/en not_active Expired - Lifetime
-
2000
- 2000-08-24 WO PCT/CA2000/000978 patent/WO2001019512A1/en not_active Ceased
- 2000-08-24 AT AT00954231T patent/ATE251945T1/de not_active IP Right Cessation
- 2000-08-24 KR KR1020027003129A patent/KR100670424B1/ko not_active Expired - Lifetime
- 2000-08-24 JP JP2001523129A patent/JP4619599B2/ja not_active Expired - Lifetime
- 2000-08-24 AU AU66783/00A patent/AU6678300A/en not_active Abandoned
- 2000-08-24 EP EP00954231A patent/EP1214146B1/de not_active Expired - Lifetime
- 2000-08-24 ES ES00954231T patent/ES2208398T3/es not_active Expired - Lifetime
- 2000-08-24 BR BRPI0013870-3A patent/BR0013870B1/pt not_active IP Right Cessation
- 2000-08-24 DE DE60005982T patent/DE60005982T2/de not_active Expired - Lifetime
- 2000-09-06 US US09/656,126 patent/US6440890B1/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JP4619599B2 (ja) | 2011-01-26 |
| ES2208398T3 (es) | 2004-06-16 |
| EP1214146B1 (de) | 2003-10-15 |
| KR20020034186A (ko) | 2002-05-08 |
| EP1214146A1 (de) | 2002-06-19 |
| WO2001019512A1 (en) | 2001-03-22 |
| DE60005982D1 (de) | 2003-11-20 |
| JP2003509388A (ja) | 2003-03-11 |
| US6440890B1 (en) | 2002-08-27 |
| BR0013870B1 (pt) | 2011-07-12 |
| KR100670424B1 (ko) | 2007-01-18 |
| BR0013870A (pt) | 2002-07-23 |
| CA2282070C (en) | 2008-12-09 |
| DE60005982T2 (de) | 2004-09-09 |
| AU6678300A (en) | 2001-04-17 |
| CA2282070A1 (en) | 2001-03-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE60005982D1 (de) | Hydrocarbylphosphinimin/cyclopentadienyl-komplexe von metallen der gruppe 4 und deren verwendung zur olefinpolymerisation | |
| Zuccaccia et al. | NOE and PGSE NMR spectroscopic studies of solution structure and aggregation in metallocenium ion-pairs | |
| Horton et al. | Controlled alkene and alkyne insertion reactivity of a cationic zirconium complex stabilized by an open diamide ligand | |
| Sellmann et al. | Nitrogenase Model Compounds:[μ‐N2H2 {Fe (“NHS4”)} 2], the Prototype for the Coordination of Diazene to Iron Sulfur Centers and Its Stabilization through Strong N H ⃛ S Hydrogen Bonds | |
| Leatherman et al. | Ni (II)-catalyzed polymerization of trans-2-butene | |
| Knijnenburg et al. | Reaction of the diimine pyridine ligand with aluminum alkyls: an unexpectedly complex reaction | |
| Vollmerhaus et al. | Ethylene Polymerization Using β-Diketimine Complexes of Zirconium | |
| Yue et al. | Zirconium phosphinimide complexes: synthesis, structure, and deactivation pathways in ethylene polymerization catalysis | |
| Sinnema et al. | Non-bridged amido cyclopentadienyl complexes of titanium: synthesis, characterization, and olefin polymerization catalysis | |
| Razavi et al. | Preparation and crystal structures of the complexes (η5-C5H3TMS–CMe2–η5-C13H8) MCl2 and [3, 6-ditButC13H6–SiMe2–NtBu] MCl2 (M= Hf, Zr or Ti): Mechanistic aspects of the catalytic formation of a isotactic–syndiotactic stereoblock-type polypropylene | |
| Herzog et al. | Reactions of [(C5Me5) ZrF3] with AlMe3–Synthesis and Structure of a Zirconium–Aluminum–Carbon Cluster | |
| Liang et al. | Nickel (II) complexes containing bidentate diarylamido phosphine ligands | |
| KR960022548A (ko) | 메탈로센 화합물 및 촉매 성분으로의 이의 용도 | |
| Chirik et al. | Preparation of ansa-niobocene and ansa-tantalocene olefin hydride complexes as transition state analogues in metallocene-catalyzed olefin polymerization | |
| Liu et al. | Tricoordinate Organochromium (III) Complexes Supported by a Bulky Silylamido Ligand Produce Ultra‐High‐Molecular Weight Polyethylene in the Absence of Activators | |
| Kim et al. | Activation of enamido zirconium complexes for ethylene polymerization: Electrophilic addition versus electrophilic abstraction reaction | |
| Deelman et al. | Lithium Derivatives of Novel Monoanionic Di-N, N ‘-chelating Pyridyl-and Quinolyl-1-azaallyl Ligands | |
| Dash et al. | Amine Elimination Reactions between Homoleptic Silylamide Lanthanide Complexes and an Isopropylidene-Bridged Cyclopentadiene− Fluorene System | |
| Götz et al. | Ternary metallocene catalyst systems based on metallocene dichlorides and AlBu3i/[PhNMe2H][B (C6F5) 4]: NMR investigations of the influence of Al/Zr ratios on alkylation and on formation of the precursor of the active metallocene species | |
| Amor et al. | Remarkably robust group 4 metal half-Sandwich complexes containing two higher alkyl ligands: x-ray structure and reactivity of the Di-n-butyl complex [Hf (η5: η1: η1-C5Me4SiMe2NCH2CH2OMe) nBu2] | |
| Stephan et al. | An approach to catalyst design: cyclopentadienyl-titanium phosphinimide complexes in ethylene polymerization | |
| Wieser et al. | Methyl-versus-chloride exchange as a measure of electron density at the metal center of ring-substituted zirconocene complexes | |
| Pietryga et al. | Main group “constrained geometry” complexes | |
| Voth et al. | Yttrium alkyl and hydrido complexes containing a tridentate-linked amido-cyclopentadienyl ligand | |
| Okamoto et al. | Structure of triaqua (nitrilotriacetato) vanadium (III) tetrahydrate |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |