JP2006509064A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2006509064A5 JP2006509064A5 JP2004556159A JP2004556159A JP2006509064A5 JP 2006509064 A5 JP2006509064 A5 JP 2006509064A5 JP 2004556159 A JP2004556159 A JP 2004556159A JP 2004556159 A JP2004556159 A JP 2004556159A JP 2006509064 A5 JP2006509064 A5 JP 2006509064A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- alkyl
- same
- mol
- periodic table
- 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
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 9
- 229920001577 copolymer Polymers 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 230000000737 periodic effect Effects 0.000 claims 7
- 239000004711 α-olefin Substances 0.000 claims 7
- 125000005842 heteroatom Chemical group 0.000 claims 6
- 229920006395 saturated elastomer Polymers 0.000 claims 6
- 125000002877 alkyl aryl group Chemical group 0.000 claims 5
- 125000003710 aryl alkyl group Chemical group 0.000 claims 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims 5
- 241000257303 Hymenoptera Species 0.000 claims 4
- 125000004429 atom Chemical group 0.000 claims 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 3
- 125000003968 arylidene group Chemical group [H]C(c)=* 0.000 claims 3
- 150000002430 hydrocarbons Chemical group 0.000 claims 3
- 125000001118 alkylidene group Chemical group 0.000 claims 2
- 229920000642 polymer Polymers 0.000 claims 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 1
- 229910052768 actinide Inorganic materials 0.000 claims 1
- 150000001255 actinides Chemical class 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 150000001768 cations Chemical class 0.000 claims 1
- 230000014509 gene expression Effects 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 238000003780 insertion Methods 0.000 claims 1
- 230000037431 insertion Effects 0.000 claims 1
- 229910052747 lanthanoid Inorganic materials 0.000 claims 1
- 150000002602 lanthanoids Chemical class 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- 125000003906 silylidene group Chemical group [H][Si]([H])=* 0.000 claims 1
- 229910052723 transition metal Inorganic materials 0.000 claims 1
- 150000003624 transition metals Chemical class 0.000 claims 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 14
- OSCBARYHPZZEIS-UHFFFAOYSA-N phenoxyboronic acid Chemical compound OB(O)OC1=CC=CC=C1 OSCBARYHPZZEIS-UHFFFAOYSA-N 0.000 description 9
- LWNGJAHMBMVCJR-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenoxy)boronic acid Chemical compound OB(O)OC1=C(F)C(F)=C(F)C(F)=C1F LWNGJAHMBMVCJR-UHFFFAOYSA-N 0.000 description 6
- IMFACGCPASFAPR-UHFFFAOYSA-O tributylazanium Chemical compound CCCC[NH+](CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-O 0.000 description 6
- 150000004645 aluminates Chemical class 0.000 description 5
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 4
- JLTDJTHDQAWBAV-UHFFFAOYSA-O dimethyl(phenyl)azanium Chemical compound C[NH+](C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-O 0.000 description 3
- OLFPYUPGPBITMH-UHFFFAOYSA-N tritylium Chemical compound C1=CC=CC=C1[C+](C=1C=CC=CC=1)C1=CC=CC=C1 OLFPYUPGPBITMH-UHFFFAOYSA-N 0.000 description 3
- HTGQCLJTWPSFNL-UHFFFAOYSA-N (2-methylphenoxy)boronic acid Chemical compound CC1=CC=CC=C1OB(O)O HTGQCLJTWPSFNL-UHFFFAOYSA-N 0.000 description 2
- BOXSCYUXSBYGRD-UHFFFAOYSA-N cyclopenta-1,3-diene;iron(3+) Chemical compound [Fe+3].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 BOXSCYUXSBYGRD-UHFFFAOYSA-N 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- LKWLQPNRJQQVEB-UHFFFAOYSA-N (2,3-dimethylphenoxy)boronic acid Chemical compound CC1=CC=CC(OB(O)O)=C1C LKWLQPNRJQQVEB-UHFFFAOYSA-N 0.000 description 1
- PHBVXHIVWULVNF-UHFFFAOYSA-N (4-fluorophenoxy)boronic acid Chemical compound OB(O)OC1=CC=C(F)C=C1 PHBVXHIVWULVNF-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- UVSSPWOKVSKHCU-UHFFFAOYSA-N [2-(trifluoromethyl)phenoxy]boronic acid Chemical compound OB(O)OC1=CC=CC=C1C(F)(F)F UVSSPWOKVSKHCU-UHFFFAOYSA-N 0.000 description 1
- GGSUCNLOZRCGPQ-UHFFFAOYSA-O diethyl(phenyl)azanium Chemical compound CC[NH+](CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-O 0.000 description 1
- GPAYUJZHTULNBE-UHFFFAOYSA-O diphenylphosphanium Chemical compound C=1C=CC=CC=1[PH2+]C1=CC=CC=C1 GPAYUJZHTULNBE-UHFFFAOYSA-O 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-O triethylphosphanium Chemical compound CC[PH+](CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-O 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- RIOQSEWOXXDEQQ-UHFFFAOYSA-O triphenylphosphanium Chemical compound C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-O 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- GIIXTFIYICRGMZ-UHFFFAOYSA-N tris(2,3-dimethylphenyl)phosphane Chemical compound CC1=CC=CC(P(C=2C(=C(C)C=CC=2)C)C=2C(=C(C)C=CC=2)C)=C1C GIIXTFIYICRGMZ-UHFFFAOYSA-N 0.000 description 1
- COIOYMYWGDAQPM-UHFFFAOYSA-N tris(2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)C1=CC=CC=C1C COIOYMYWGDAQPM-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02080121 | 2002-12-04 | ||
| US43180202P | 2002-12-09 | 2002-12-09 | |
| PCT/EP2003/012944 WO2004050713A2 (en) | 2002-12-04 | 2003-11-14 | 1-buten copolymers and process for preparing them |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006509064A JP2006509064A (ja) | 2006-03-16 |
| JP2006509064A5 true JP2006509064A5 (enExample) | 2006-12-07 |
Family
ID=46124008
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004556159A Pending JP2006509064A (ja) | 2002-12-04 | 2003-11-14 | １−ブテンコポリマー類およびそれらの製造方法 |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP1567568B1 (enExample) |
| JP (1) | JP2006509064A (enExample) |
| KR (1) | KR101021829B1 (enExample) |
| AT (1) | ATE444315T1 (enExample) |
| AU (1) | AU2003296585A1 (enExample) |
| WO (1) | WO2004050713A2 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7459511B2 (en) | 2001-06-12 | 2008-12-02 | Basell Polyolefine Gmbh | Process for the polymerization of 1-butene |
| WO2004033510A2 (en) | 2002-10-10 | 2004-04-22 | Basell Polyolefine Gmbh | Process for the copolymerization of ethylene |
| US7589160B2 (en) | 2002-12-04 | 2009-09-15 | Basell Polyolefine Gmbh | Process for preparing 1-butene polymers |
| WO2005095473A1 (en) * | 2004-03-12 | 2005-10-13 | Basell Polyolefine Gmbh | Process for polymerizing 1-hexene or higher alpha-olefins |
| CA2573984A1 (en) | 2004-07-22 | 2006-01-26 | Basell Polyolefine Gmbh | Process for producing fractionable 1-butene polymers |
| PL1769030T3 (pl) * | 2004-07-22 | 2008-08-29 | Basell Polyolefine Gmbh | Kompozycja polimerów 1-butenu |
| EP1655314A1 (en) * | 2004-11-09 | 2006-05-10 | Basell Polyolefine GmbH | Process for the preparation of 1-butene/propylene copolymers |
| DE602005015479D1 (de) * | 2004-11-09 | 2009-08-27 | Basell Polyolefine Gmbh | Verfahren zur herstellung von 1-buten/propylen-copolymeren |
| KR20070093058A (ko) * | 2004-11-22 | 2007-09-17 | 바젤 폴리올레핀 게엠베하 | 프로필렌 기재 삼중합체 |
| EP2057226B1 (en) * | 2006-08-30 | 2009-12-09 | Basell Polyolefine GmbH | 1-butene propylene copolymer compositions |
| JP5580589B2 (ja) * | 2006-08-30 | 2014-08-27 | バーゼル・ポリオレフィン・ゲーエムベーハー | １−ブテンプロピレンコポリマー組成物 |
| KR20100127226A (ko) * | 2008-03-20 | 2010-12-03 | 바셀 폴리올레핀 이탈리아 에스.알.엘 | 1-부텐 공중합체 |
| BRPI0908997A2 (pt) | 2008-03-20 | 2015-08-04 | Basell Poliolefine Srl | Composições de polímeros à base de 1-buteno |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60262804A (ja) * | 1984-06-11 | 1985-12-26 | Mitsui Petrochem Ind Ltd | ポリ１−ブテン樹脂 |
| JPH06104699B2 (ja) * | 1985-11-20 | 1994-12-21 | 三井石油化学工業株式会社 | １―ブテン系ランダム共重合体およびそれからなる熱可塑性樹脂用ヒートシール性改善剤 |
| JPH0753767B2 (ja) * | 1985-11-22 | 1995-06-07 | 三井石油化学工業株式会社 | α−オレフイン系ランダム共重合体の製造法 |
| JPH0816133B2 (ja) * | 1987-03-14 | 1996-02-21 | 出光石油化学株式会社 | ブテン−１共重合体 |
| JPH0816131B2 (ja) * | 1987-03-19 | 1996-02-21 | 出光石油化学株式会社 | ブテン系共重合体 |
| DE59104869D1 (de) * | 1990-11-12 | 1995-04-13 | Hoechst Ag | 2-Substituierte Bisindenylmetallocene, Verfahren zu ihrer Herstellung und ihre Verwendung als Katalysatoren bei der Olefinpolymerisation. |
| ES2139217T3 (es) * | 1994-06-09 | 2000-02-01 | Infineum Usa Lp | Procedimiento diluido para la polimerizacion de homopolimeros y copolimeros de alfa-olefina no etilenica que usa sistemas cataliticos de metaloceno. |
| RU2219190C2 (ru) * | 1998-03-05 | 2003-12-20 | Монтелл Текнолоджи Компани Б.В. | (со)полимеры полибутена-1 и способ их получения |
| US6444833B1 (en) * | 1999-12-15 | 2002-09-03 | Basell Technology Company Bv | Metallocene compounds, process for their preparation and their use in catalytic systems for the polymerization of olefins |
| CN1280300C (zh) * | 1999-12-28 | 2006-10-18 | 巴塞尔技术有限公司 | 杂环茂金属化合物及其在生产烯烃聚合物的催化剂体系中的用途 |
| JP4902050B2 (ja) * | 2000-11-24 | 2012-03-21 | 出光興産株式会社 | ポリオレフィン系樹脂組成物とその成形体及びフィルム |
| ATE444975T1 (de) * | 2001-06-12 | 2009-10-15 | Basell Polyolefine Gmbh | Verfahren zur polymerisation von buten-1 |
| US7459511B2 (en) * | 2001-06-12 | 2008-12-02 | Basell Polyolefine Gmbh | Process for the polymerization of 1-butene |
| EP1446430B1 (en) * | 2001-11-12 | 2007-02-07 | Basell Polyolefine GmbH | Process for polymerizing 1-butene and 1-butene polymers |
-
2003
- 2003-11-14 KR KR1020057010235A patent/KR101021829B1/ko not_active Expired - Lifetime
- 2003-11-14 WO PCT/EP2003/012944 patent/WO2004050713A2/en not_active Ceased
- 2003-11-14 AT AT03812152T patent/ATE444315T1/de not_active IP Right Cessation
- 2003-11-14 EP EP03812152A patent/EP1567568B1/en not_active Expired - Lifetime
- 2003-11-14 JP JP2004556159A patent/JP2006509064A/ja active Pending
- 2003-11-14 AU AU2003296585A patent/AU2003296585A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2004529254A5 (enExample) | ||
| US9266910B2 (en) | Asymmetric polypropylene catalysts | |
| US10519259B2 (en) | Low melting PP homopolymer with high content of regioerrors and high molecular weight | |
| JP2006509059A5 (enExample) | ||
| JP6216887B2 (ja) | 低温における耐衝撃性が改善されたプロピレン組成物 | |
| JP2008535799A5 (enExample) | ||
| JP2006526042A5 (enExample) | ||
| JP2020511423A5 (enExample) | ||
| US20210332227A1 (en) | Propylene random copolymer for use in film applications | |
| US6448349B1 (en) | Syndiotactic/atactic block polyolefins, catalysts and processes for producing the same | |
| US20210347971A1 (en) | Propylene copolymer with excellent optical properties | |
| JP2007505173A5 (enExample) | ||
| JP2009534489A5 (enExample) | ||
| JP2008534705A5 (enExample) | ||
| EP3063184B1 (en) | Asymmetric catalysts for olefin polymerisation | |
| JP2004530029A5 (enExample) | ||
| JP3672500B2 (ja) | ポリプロピレン樹脂組成物およびその用途 | |
| KR102559050B1 (ko) | 프로필렌-1-부텐 공중합체 및 그 제조방법 | |
| RU2365605C2 (ru) | Полипропиленовая композиция | |
| JP2008536813A5 (enExample) | ||
| CN113039218A (zh) | 用于丙烯聚合的负载催化剂及利用它的聚丙烯树脂制备方法 | |
| RU2007106716A (ru) | Способ получения фракционируемых полимеров 1-бутена | |
| JP2008506825A5 (enExample) | ||
| JP2004534829A5 (enExample) | ||
| JP2008506663A5 (enExample) |