JP2001527086A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2001527086A5 JP2001527086A5 JP2000526528A JP2000526528A JP2001527086A5 JP 2001527086 A5 JP2001527086 A5 JP 2001527086A5 JP 2000526528 A JP2000526528 A JP 2000526528A JP 2000526528 A JP2000526528 A JP 2000526528A JP 2001527086 A5 JP2001527086 A5 JP 2001527086A5
- Authority
- JP
- Japan
- Prior art keywords
- spacer
- cyclo
- transition metal
- substituted
- saturated
- 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.)
- Pending
Links
- 150000001875 compounds Chemical class 0.000 description 13
- 125000006850 spacer group Chemical group 0.000 description 13
- 229910052723 transition metal Inorganic materials 0.000 description 9
- 150000003624 transition metals Chemical class 0.000 description 9
- -1 1-thienyl Chemical group 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 5
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- 229910052711 selenium Inorganic materials 0.000 description 5
- 239000011669 selenium Substances 0.000 description 5
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 4
- 229910052785 arsenic Inorganic materials 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 4
- 238000007334 copolymerization reaction Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 239000002841 Lewis acid Substances 0.000 description 2
- 239000002879 Lewis base Substances 0.000 description 2
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 150000001345 alkine derivatives Chemical class 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 2
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001925 cycloalkenes Chemical class 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- 229910052733 gallium Inorganic materials 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 229910052747 lanthanoid Inorganic materials 0.000 description 2
- 150000002602 lanthanoids Chemical class 0.000 description 2
- 150000007517 lewis acids Chemical class 0.000 description 2
- 150000007527 lewis bases Chemical class 0.000 description 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Chemical class C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 2
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 229920001567 vinyl ester resin Polymers 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- GGNVFGDIHCZNPQ-UHFFFAOYSA-N $l^{1}-selanylamine Chemical compound [Se]N GGNVFGDIHCZNPQ-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- 239000007848 Bronsted acid Substances 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229910052768 actinide Inorganic materials 0.000 description 1
- 150000001255 actinides Chemical class 0.000 description 1
- 229910000086 alane Inorganic materials 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- XQJHRCVXRAJIDY-UHFFFAOYSA-N aminophosphine Chemical class PN XQJHRCVXRAJIDY-UHFFFAOYSA-N 0.000 description 1
- 150000001450 anions Chemical group 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- NDXGGKDTNFVFGA-UHFFFAOYSA-N arsinous amide Chemical compound [AsH2]N NDXGGKDTNFVFGA-UHFFFAOYSA-N 0.000 description 1
- VUEDNLCYHKSELL-UHFFFAOYSA-N arsonium Chemical compound [AsH4+] VUEDNLCYHKSELL-UHFFFAOYSA-N 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- 229910000085 borane Inorganic materials 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical group [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical class C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 1
- 125000003983 fluorenyl group Chemical class C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 239000002638 heterogeneous catalyst Substances 0.000 description 1
- 150000002469 indenes Chemical class 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- RSPCKAHMRANGJZ-UHFFFAOYSA-N thiohydroxylamine Chemical compound SN RSPCKAHMRANGJZ-UHFFFAOYSA-N 0.000 description 1
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19757524.2 | 1997-12-23 | ||
| DE19757524A DE19757524A1 (de) | 1997-12-23 | 1997-12-23 | eta-Komplex-Verbindungen |
| PCT/EP1998/008074 WO1999033852A1 (de) | 1997-12-23 | 1998-12-10 | π-KOMPLEX-VERBINDUNGEN |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2001527086A JP2001527086A (ja) | 2001-12-25 |
| JP2001527086A5 true JP2001527086A5 (enExample) | 2006-02-09 |
Family
ID=7853175
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000526528A Pending JP2001527086A (ja) | 1997-12-23 | 1998-12-10 | π錯体化合物 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6433112B1 (enExample) |
| EP (1) | EP1042336B1 (enExample) |
| JP (1) | JP2001527086A (enExample) |
| KR (1) | KR100573338B1 (enExample) |
| CN (1) | CN1238362C (enExample) |
| AT (1) | ATE215546T1 (enExample) |
| AU (1) | AU2270699A (enExample) |
| CA (1) | CA2315805A1 (enExample) |
| DE (2) | DE19757524A1 (enExample) |
| ES (1) | ES2177132T3 (enExample) |
| NO (1) | NO20003135L (enExample) |
| RU (1) | RU2214414C2 (enExample) |
| TW (1) | TW503245B (enExample) |
| WO (1) | WO1999033852A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19915108A1 (de) * | 1999-04-01 | 2000-10-05 | Bayer Ag | Geträgerte Katalysatoren mit einer Donor-Akzeptor-Wechselwirkung |
| DE10114345A1 (de) * | 2001-03-23 | 2002-09-26 | Bayer Ag | Katalysator mit einer Donor-Akzeptor-Wechselwirkung |
| DE10244214A1 (de) * | 2002-09-23 | 2004-04-01 | Bayer Ag | Übergangsmetallverbindungen mit Donor-Akzeptor-Wechselwirkung und speziellem Substitutionsmuster |
| CN103889992B (zh) * | 2011-08-02 | 2016-08-31 | 罗克伍德锂有限责任公司 | 均配稀土三芳基配合物 |
| WO2013017280A1 (de) * | 2011-08-02 | 2013-02-07 | Chemetall Gmbh | η5:η1-CYCLOPENTADIENYLIDEN-PHOSPHORAN-CONSTRAINED-GEOMETRY-KOMPLEXE DER SELTENERD-METALLE |
| CN114552019A (zh) * | 2022-03-18 | 2022-05-27 | 杭州怡莱珂科技有限公司 | 一种络阴离子钠盐及其制备方法与使用方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ZA844157B (en) | 1983-06-06 | 1986-01-29 | Exxon Research Engineering Co | Process and catalyst for polyolefin density and molecular weight control |
| NZ235032A (en) | 1989-08-31 | 1993-04-28 | Dow Chemical Co | Constrained geometry complexes of titanium, zirconium or hafnium comprising a substituted cyclopentadiene ligand; use as olefin polymerisation catalyst component |
| US5026798A (en) | 1989-09-13 | 1991-06-25 | Exxon Chemical Patents Inc. | Process for producing crystalline poly-α-olefins with a monocyclopentadienyl transition metal catalyst system |
| DE4139261A1 (de) | 1991-11-29 | 1993-06-03 | Basf Ag | Ethylen-copolymerisate niederer dichte |
| WO1993014132A1 (en) | 1992-01-06 | 1993-07-22 | The Dow Chemical Company | Improved catalyst composition |
| WO1993021242A1 (en) * | 1992-04-20 | 1993-10-28 | Exxon Chemical Patents Inc. | Ethylene/branched olefin copolymers |
| US5635573A (en) * | 1992-12-01 | 1997-06-03 | Exxon Chemical Patents Inc. | Method for preparing alpha-olefin/cycloolefin copolymers |
| GB9304521D0 (en) | 1993-03-05 | 1993-04-21 | Exxon Chemical Patents Inc | Improved alumoxane,method for its preparation and polymerisation process using such alumoxane |
| US5470993A (en) | 1993-06-24 | 1995-11-28 | The Dow Chemical Company | Titanium(II) or zirconium(II) complexes and addition polymerization catalysts therefrom |
| EP0638593A1 (en) * | 1993-08-02 | 1995-02-15 | Shell Internationale Researchmaatschappij B.V. | Catalyst compositions |
| MY112177A (en) | 1994-09-30 | 2001-04-30 | Mitsui Chemicals Inc | Olefin polymerization catalyst and process for olefin polymerization |
| CN1171794A (zh) | 1994-10-31 | 1998-01-28 | Dsm有限公司 | 用于烯烃聚合的催化剂组合物及方法 |
-
1997
- 1997-12-23 DE DE19757524A patent/DE19757524A1/de not_active Withdrawn
-
1998
- 1998-12-10 CN CNB988137755A patent/CN1238362C/zh not_active Expired - Fee Related
- 1998-12-10 CA CA002315805A patent/CA2315805A1/en not_active Abandoned
- 1998-12-10 JP JP2000526528A patent/JP2001527086A/ja active Pending
- 1998-12-10 ES ES98966295T patent/ES2177132T3/es not_active Expired - Lifetime
- 1998-12-10 WO PCT/EP1998/008074 patent/WO1999033852A1/de not_active Ceased
- 1998-12-10 EP EP98966295A patent/EP1042336B1/de not_active Expired - Lifetime
- 1998-12-10 DE DE59803673T patent/DE59803673D1/de not_active Expired - Fee Related
- 1998-12-10 KR KR1020007006968A patent/KR100573338B1/ko not_active Expired - Fee Related
- 1998-12-10 RU RU2000119764/04A patent/RU2214414C2/ru not_active IP Right Cessation
- 1998-12-10 AT AT98966295T patent/ATE215546T1/de not_active IP Right Cessation
- 1998-12-10 AU AU22706/99A patent/AU2270699A/en not_active Abandoned
- 1998-12-10 US US09/581,973 patent/US6433112B1/en not_active Expired - Fee Related
- 1998-12-11 TW TW087120580A patent/TW503245B/zh not_active IP Right Cessation
-
2000
- 2000-06-16 NO NO20003135A patent/NO20003135L/no not_active Application Discontinuation
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP3010349B2 (ja) | 付加重合触媒及び付加重合方法 | |
| US6184320B1 (en) | Method for producing metallocene compounds formed by two carbanions | |
| EP0705851B9 (en) | Catalyst systems and process for producing broad molecular weight distribution polyolefin | |
| CA2259434C (en) | Method for producing elastomers | |
| WO1992009640A1 (fr) | Procede de production de polymere olefinique | |
| US6479646B1 (en) | Metallocene compounds having indenyl ligand and catalysts for olefin polymerization containing the same | |
| CN1248979A (zh) | 烯烃聚合的方法 | |
| JP2001527086A5 (enExample) | ||
| US6353064B1 (en) | Supported catalysts with a donor-acceptor interaction | |
| JP3493235B2 (ja) | エチレン系重合体の製造方法及びその方法により得られたエチレン系重合体 | |
| US6433112B1 (en) | π-complex compounds | |
| CA2113806A1 (en) | Method for the preparation of polyolefin | |
| JP2004534740A (ja) | ドナー−アクセプター相互作用を特徴とする触媒 | |
| CA2315651A1 (en) | Method for producing elastomers | |
| JPWO1993024541A1 (ja) | ポリオレフィンの製造方法 | |
| US6423659B1 (en) | π-complex compounds | |
| JP3325719B2 (ja) | エチレン重合体の製造法 | |
| US7166684B2 (en) | Transition metal compound, catalyst for olefin polymerization and method for producing polyolefin | |
| US20040059073A1 (en) | Transition metal compounds having a donor-acceptor interaction and a specific substitution pattern | |
| KR100523497B1 (ko) | 메탈로센화합물 | |
| KR100480849B1 (ko) | 공업용시클로올레핀(공)중합체의제조방법 | |
| JP4035860B2 (ja) | 有機遷移金属化合物、それを用いたオレフィン重合用触媒およびそれを用いたポリオレフィンの製造方法 | |
| JP3255710B2 (ja) | オレフィン系重合体の製造方法およびオレフィン系重合触媒 | |
| JP4245864B2 (ja) | オレフィン重合用触媒及び該触媒を用いる重合方法 | |
| JP3070256B2 (ja) | オレフィン重合体の製造方法 |