JP2005514424A5 - - Google Patents
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- Publication number
- JP2005514424A5 JP2005514424A5 JP2003558020A JP2003558020A JP2005514424A5 JP 2005514424 A5 JP2005514424 A5 JP 2005514424A5 JP 2003558020 A JP2003558020 A JP 2003558020A JP 2003558020 A JP2003558020 A JP 2003558020A JP 2005514424 A5 JP2005514424 A5 JP 2005514424A5
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- group
- saturated
- alkyl
- 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.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims description 23
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 17
- 229910052744 lithium Inorganic materials 0.000 claims description 15
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 14
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical group [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 14
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 14
- 229910052700 potassium Chemical group 0.000 claims description 14
- 239000011591 potassium Chemical group 0.000 claims description 14
- 229910052708 sodium Inorganic materials 0.000 claims description 14
- 239000011734 sodium Chemical group 0.000 claims description 14
- 239000002168 alkylating agent Substances 0.000 claims description 13
- 229940100198 alkylating agent Drugs 0.000 claims description 13
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 11
- 229910052794 bromium Inorganic materials 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 10
- 239000000460 chlorine Substances 0.000 claims description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 9
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 9
- 125000005843 halogen group Chemical group 0.000 claims description 9
- 229910052740 iodine Inorganic materials 0.000 claims description 9
- 239000011630 iodine Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 239000003513 alkali Substances 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- 150000001340 alkali metals Chemical group 0.000 claims description 5
- 150000004678 hydrides Chemical class 0.000 claims description 5
- 239000003446 ligand Substances 0.000 claims description 5
- 230000003647 oxidation Effects 0.000 claims description 5
- 238000007254 oxidation reaction Methods 0.000 claims description 5
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 229920006395 saturated elastomer Polymers 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 125000003118 aryl group Chemical group 0.000 claims 7
- 125000002877 alkyl aryl group Chemical group 0.000 claims 5
- 125000005842 heteroatom Chemical group 0.000 claims 5
- 230000000737 periodic effect Effects 0.000 claims 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 239000010703 silicon Substances 0.000 claims 2
- 229910052768 actinide Inorganic materials 0.000 claims 1
- 150000001255 actinides Chemical class 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims 1
- 229910052747 lanthanoid Inorganic materials 0.000 claims 1
- 150000002602 lanthanoids Chemical class 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 229910052723 transition metal Inorganic materials 0.000 claims 1
- 150000003624 transition metals Chemical class 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000010 aprotic solvent Substances 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 125000006701 (C1-C7) alkyl group Chemical group 0.000 description 1
- 125000005915 C6-C14 aryl group Chemical group 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical compound C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- -1 pentadienyl Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02075040 | 2002-01-08 | ||
| PCT/EP2002/014899 WO2003057705A1 (en) | 2002-01-08 | 2002-12-30 | Preparation of silicon-bridged metallocene compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005514424A JP2005514424A (ja) | 2005-05-19 |
| JP2005514424A5 true JP2005514424A5 (enExample) | 2009-08-06 |
| JP4417719B2 JP4417719B2 (ja) | 2010-02-17 |
Family
ID=8185505
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003558020A Expired - Lifetime JP4417719B2 (ja) | 2002-01-08 | 2002-12-30 | シリコン橋状メタロセン化合物の製造 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7002031B2 (enExample) |
| EP (1) | EP1470140B1 (enExample) |
| JP (1) | JP4417719B2 (enExample) |
| AT (1) | ATE388957T1 (enExample) |
| DE (1) | DE60225595T2 (enExample) |
| WO (1) | WO2003057705A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1492825A1 (en) * | 2002-02-25 | 2005-01-05 | Basell Polyolefine GmbH | Process for the copolymerization of ethylene |
| WO2004099225A1 (en) * | 2003-05-08 | 2004-11-18 | Basell Polyolefine Gmbh | Process for the production of halide metallocene compounds |
| ES2280047T3 (es) | 2003-09-29 | 2007-09-01 | Basell Polyolefine Gmbh | Procedimiento para la isomerizacion de compuestos de metaloceno. |
| US11208514B2 (en) | 2008-03-20 | 2021-12-28 | Chevron Phillips Chemical Company Lp | Silica-coated alumina activator-supports for metallocene catalyst compositions |
| US7884163B2 (en) | 2008-03-20 | 2011-02-08 | Chevron Phillips Chemical Company Lp | Silica-coated alumina activator-supports for metallocene catalyst compositions |
| US20090240010A1 (en) * | 2008-03-20 | 2009-09-24 | Mcdaniel Max P | Alumina-silica activator-supports for metallocene catalyst compositions |
| US8895679B2 (en) | 2012-10-25 | 2014-11-25 | Chevron Phillips Chemical Company Lp | Catalyst compositions and methods of making and using same |
| US8937139B2 (en) | 2012-10-25 | 2015-01-20 | Chevron Phillips Chemical Company Lp | Catalyst compositions and methods of making and using same |
| US8877672B2 (en) | 2013-01-29 | 2014-11-04 | Chevron Phillips Chemical Company Lp | Catalyst compositions and methods of making and using same |
| US9034991B2 (en) | 2013-01-29 | 2015-05-19 | Chevron Phillips Chemical Company Lp | Polymer compositions and methods of making and using same |
| KR102064411B1 (ko) | 2016-11-22 | 2020-01-09 | 주식회사 엘지화학 | 메탈로센 담지 촉매 및 이를 이용하는 폴리프로필렌의 제조 방법 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW294669B (enExample) * | 1992-06-27 | 1997-01-01 | Hoechst Ag | |
| IT1256259B (it) | 1992-12-30 | 1995-11-29 | Montecatini Tecnologie Srl | Composti mettallocenici aventi leganti di tipo fluorenilico |
| WO1996019488A1 (en) * | 1994-12-21 | 1996-06-27 | Exxon Chemical Patents Inc. | A method of preparing high purity racemic metallocene alkyls and use thereof |
| PL330222A1 (en) * | 1997-03-29 | 1999-05-10 | Montell Technology Company Bv | Metalocenes and catalysts for use in polymerisation of olefins |
| CA2257132A1 (en) * | 1997-03-29 | 1998-10-08 | Montell Technology Company B.V. | Process for preparing cyclopentadienyl compounds |
| CN1243763C (zh) | 1998-01-14 | 2006-03-01 | 蒙特尔技术有限公司 | 茂金属化合物的制备方法 |
-
2002
- 2002-12-30 JP JP2003558020A patent/JP4417719B2/ja not_active Expired - Lifetime
- 2002-12-30 EP EP02795296A patent/EP1470140B1/en not_active Expired - Lifetime
- 2002-12-30 WO PCT/EP2002/014899 patent/WO2003057705A1/en not_active Ceased
- 2002-12-30 US US10/500,542 patent/US7002031B2/en not_active Expired - Lifetime
- 2002-12-30 DE DE60225595T patent/DE60225595T2/de not_active Expired - Lifetime
- 2002-12-30 AT AT02795296T patent/ATE388957T1/de not_active IP Right Cessation
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