JP2011122145A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2011122145A5 JP2011122145A5 JP2010253870A JP2010253870A JP2011122145A5 JP 2011122145 A5 JP2011122145 A5 JP 2011122145A5 JP 2010253870 A JP2010253870 A JP 2010253870A JP 2010253870 A JP2010253870 A JP 2010253870A JP 2011122145 A5 JP2011122145 A5 JP 2011122145A5
- Authority
- JP
- Japan
- Prior art keywords
- containing group
- group
- atom
- general formula
- bonded
- 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
Links
- 150000001875 compounds Chemical class 0.000 claims description 9
- 150000001336 alkenes Chemical class 0.000 claims 13
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 13
- -1 iso-propylphenyl Chemical group 0.000 claims 9
- 150000002430 hydrocarbons Chemical group 0.000 claims 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 8
- 125000004432 carbon atom Chemical group C* 0.000 claims 7
- 125000005843 halogen group Chemical group 0.000 claims 7
- 150000003623 transition metal compounds Chemical class 0.000 claims 7
- 239000002685 polymerization catalyst Substances 0.000 claims 6
- 229910052799 carbon Inorganic materials 0.000 claims 4
- 238000006116 polymerization reaction Methods 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 239000001301 oxygen Substances 0.000 claims 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 229910052796 boron Inorganic materials 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 229910052732 germanium Inorganic materials 0.000 claims 2
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims 2
- 150000002391 heterocyclic compounds Chemical group 0.000 claims 2
- 229910052740 iodine Inorganic materials 0.000 claims 2
- 125000002950 monocyclic group Chemical group 0.000 claims 2
- 230000000737 periodic effect Effects 0.000 claims 2
- 229910052698 phosphorus Inorganic materials 0.000 claims 2
- 239000011574 phosphorus Substances 0.000 claims 2
- 230000000379 polymerizing effect Effects 0.000 claims 2
- 229910052710 silicon Inorganic materials 0.000 claims 2
- 239000010703 silicon Substances 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 239000011593 sulfur Substances 0.000 claims 2
- 150000003624 transition metals Chemical group 0.000 claims 2
- JDHZNBMFPGNCLH-UHFFFAOYSA-N 1,4-dihydro-1,4-methanoanthracene Chemical compound C12=CC3=CC=CC=C3C=C2C2CC1C=C2 JDHZNBMFPGNCLH-UHFFFAOYSA-N 0.000 claims 1
- IEGYXSAHRKJELM-UHFFFAOYSA-N 1,4-dihydro-1,4-methanonaphthalene Chemical compound C12=CC=CC=C2C2CC1C=C2 IEGYXSAHRKJELM-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 125000001118 alkylidene group Chemical group 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical group C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 claims 1
- 150000002902 organometallic compounds Chemical class 0.000 claims 1
- 125000003367 polycyclic group Chemical group 0.000 claims 1
- 229910052719 titanium Inorganic materials 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- 239000004711 α-olefin Substances 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 239000007787 solid Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 3
- DWKNOLCXIFYNFV-HSZRJFAPSA-N 2-[[(2r)-1-[1-[(4-chloro-3-methylphenyl)methyl]piperidin-4-yl]-5-oxopyrrolidine-2-carbonyl]amino]-n,n,6-trimethylpyridine-4-carboxamide Chemical compound CN(C)C(=O)C1=CC(C)=NC(NC(=O)[C@@H]2N(C(=O)CC2)C2CCN(CC=3C=C(C)C(Cl)=CC=3)CC2)=C1 DWKNOLCXIFYNFV-HSZRJFAPSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000010898 silica gel chromatography Methods 0.000 description 2
- NYNZQNWKBKUAII-KBXCAEBGSA-N (3s)-n-[5-[(2r)-2-(2,5-difluorophenyl)pyrrolidin-1-yl]pyrazolo[1,5-a]pyrimidin-3-yl]-3-hydroxypyrrolidine-1-carboxamide Chemical compound C1[C@@H](O)CCN1C(=O)NC1=C2N=C(N3[C@H](CCC3)C=3C(=CC=C(F)C=3)F)C=CN2N=C1 NYNZQNWKBKUAII-KBXCAEBGSA-N 0.000 description 1
- MYWSBJKVOUZCIA-UHFFFAOYSA-N 2-hydroxy-3,5-diiodobenzaldehyde Chemical compound OC1=C(I)C=C(I)C=C1C=O MYWSBJKVOUZCIA-UHFFFAOYSA-N 0.000 description 1
- MJKNHXCPGXUEDO-UHFFFAOYSA-N 3,5-ditert-butylaniline Chemical compound CC(C)(C)C1=CC(N)=CC(C(C)(C)C)=C1 MJKNHXCPGXUEDO-UHFFFAOYSA-N 0.000 description 1
- STBGLXMINLWCNL-UHFFFAOYSA-N 3-bromo-2-hydroxybenzaldehyde Chemical compound OC1=C(Br)C=CC=C1C=O STBGLXMINLWCNL-UHFFFAOYSA-N 0.000 description 1
- UXHQLGLGLZKHTC-CUNXSJBXSA-N 4-[(3s,3ar)-3-cyclopentyl-7-(4-hydroxypiperidine-1-carbonyl)-3,3a,4,5-tetrahydropyrazolo[3,4-f]quinolin-2-yl]-2-chlorobenzonitrile Chemical compound C1CC(O)CCN1C(=O)C1=CC=C(C=2[C@@H]([C@H](C3CCCC3)N(N=2)C=2C=C(Cl)C(C#N)=CC=2)CC2)C2=N1 UXHQLGLGLZKHTC-CUNXSJBXSA-N 0.000 description 1
- WRDWWAVNELMWAM-UHFFFAOYSA-N 4-tert-butylaniline Chemical compound CC(C)(C)C1=CC=C(N)C=C1 WRDWWAVNELMWAM-UHFFFAOYSA-N 0.000 description 1
- XULSCZPZVQIMFM-IPZQJPLYSA-N odevixibat Chemical compound C12=CC(SC)=C(OCC(=O)N[C@@H](C(=O)N[C@@H](CC)C(O)=O)C=3C=CC(O)=CC=3)C=C2S(=O)(=O)NC(CCCC)(CCCC)CN1C1=CC=CC=C1 XULSCZPZVQIMFM-IPZQJPLYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010253870A JP5597102B2 (ja) | 2009-11-13 | 2010-11-12 | 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 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009260312 | 2009-11-13 | ||
| JP2009260312 | 2009-11-13 | ||
| JP2010253870A JP5597102B2 (ja) | 2009-11-13 | 2010-11-12 | 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 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011122145A JP2011122145A (ja) | 2011-06-23 |
| JP2011122145A5 true JP2011122145A5 (enrdf_load_stackoverflow) | 2013-10-31 |
| JP5597102B2 JP5597102B2 (ja) | 2014-10-01 |
Family
ID=44286334
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010253870A Active JP5597102B2 (ja) | 2009-11-13 | 2010-11-12 | 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 |
| JP2010253871A Active JP5597103B2 (ja) | 2009-11-13 | 2010-11-12 | 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 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010253871A Active JP5597103B2 (ja) | 2009-11-13 | 2010-11-12 | 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 |
Country Status (1)
| Country | Link |
|---|---|
| JP (2) | JP5597102B2 (enrdf_load_stackoverflow) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6129598B2 (ja) * | 2013-03-17 | 2017-05-17 | 日本ポリエチレン株式会社 | ジオール化合物及びそれを用いるオレフィン重合用触媒並びにオレフィン重合体の製造方法 |
| US11560384B2 (en) | 2017-05-04 | 2023-01-24 | University Of Utah Research Foundation | Benzonorbornadiene derivatives and reactions thereof |
| KR102100142B1 (ko) * | 2017-12-21 | 2020-04-14 | 사빅 에스케이 넥슬렌 컴퍼니 피티이 엘티디 | 금속-리간드 착체, 이를 포함하는 에틸렌계 중합용 촉매 조성물 및 이를 이용한 에틸렌계 중합체의 제조방법 |
| JP7175692B2 (ja) * | 2018-03-26 | 2022-11-21 | 三井化学株式会社 | 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 |
| WO2020137710A1 (ja) * | 2018-12-27 | 2020-07-02 | 三井化学株式会社 | 医療用器具用環状オレフィン共重合体、医療用器具用環状オレフィン共重合体組成物、および成形体 |
| JP2022158626A (ja) * | 2021-04-02 | 2022-10-17 | 株式会社クラレ | 重合体の製造方法、ラジカル重合用組成物及びラジカル重合制御剤 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6410664B1 (en) * | 1997-03-24 | 2002-06-25 | Cryovac, Inc. | Catalyst compositions and processes for olefin polymers and copolymers |
| JP3900699B2 (ja) * | 1998-08-12 | 2007-04-04 | 三井化学株式会社 | オレフィン重合用触媒およびオレフィンの重合方法 |
| JP2000119313A (ja) * | 1998-10-09 | 2000-04-25 | Mitsui Chemicals Inc | オレフィンの重合方法 |
| JP2000191712A (ja) * | 1998-12-28 | 2000-07-11 | Mitsui Chemicals Inc | オレフィン重合触媒とオレフィン重合方法 |
| JP2004331965A (ja) * | 2003-04-18 | 2004-11-25 | Mitsui Chemicals Inc | 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 |
| JP2006219536A (ja) * | 2005-02-08 | 2006-08-24 | Mitsui Chemicals Inc | 末端官能基含有ポリオレフィンの製造方法 |
| EP1834970B1 (en) * | 2006-03-15 | 2014-05-14 | Styrolution GmbH | A process for producing polyolefin-polyvinylaromatic-block copolymers |
| JP2007297453A (ja) * | 2006-04-28 | 2007-11-15 | Mitsui Chemicals Inc | オレフィン重合用触媒およびオレフィンの重合方法 |
| WO2009076152A1 (en) * | 2007-12-05 | 2009-06-18 | The Polymer Technology Group, Inc. | Mixture of polyethylene-co-syndiotactic polypropylene block co-polymer and ultrahigh molecular weight polyethylene |
-
2010
- 2010-11-12 JP JP2010253870A patent/JP5597102B2/ja active Active
- 2010-11-12 JP JP2010253871A patent/JP5597103B2/ja active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2011122145A5 (enrdf_load_stackoverflow) | ||
| EP2231686B1 (en) | Process for one-pot synthesis of 1,1-diphenyl-1-(3-substituted-cyclopentadienyl)-1-(2,7-di-t-butyl-fluoren-9-yl)methane type ligands | |
| JP6688382B2 (ja) | メタロセン化合物及びその製造方法 | |
| Park et al. | Preparation of ansa-metallocenes for production of poly (α-olefin) lubricants | |
| KR20130056247A (ko) | 알킬 시클로펜타디엔 화합물의 합성 | |
| US20110003953A1 (en) | Carbon-Bridged Cyclopentadienyl-Fluorenyl Ligands | |
| JP5019517B2 (ja) | 二核金属錯体およびその製造方法 | |
| TW200533676A (en) | Catalyst components and their use in the polymerization of olefins | |
| JP2022191351A (ja) | 二座ホスフィン配位子を有するロジウム錯体及びその製造方法、並びに二座ホスフィン配位子を有するロジウム錯体を用いるハロゲン化アリルのヒドロシリル化 | |
| JPWO2012077289A1 (ja) | メソ型及びラセミ型メタロセン錯体の製造方法 | |
| JP5957616B2 (ja) | 新規なリガンド化合物、その製造方法、遷移金属化合物、およびその製造方法 | |
| JP2014224053A5 (enrdf_load_stackoverflow) | ||
| US20060052620A1 (en) | Preparation of substituted indenes | |
| JP5959131B2 (ja) | 新規なリガンド化合物、その製造方法および前記リガンド化合物を含む遷移金属化合物、およびその製造方法 | |
| KR20170009597A (ko) | 메탈로센 화합물, 이를 포함하는 촉매 조성물 및 이를 이용한 올레핀 중합체의 제조방법 | |
| JP2022530356A (ja) | 金属－配位子錯体を作製する方法 | |
| KR101789386B1 (ko) | 고수율 및 고 광학순도의 광학활성 벤조티오펜계 화합물의 합성 방법 | |
| JP5980659B2 (ja) | カルバゾール基を有するポリマー、カルバゾール基を有するモノマー及び化合物 | |
| JP5283984B2 (ja) | 遷移金属化合物の製造方法 | |
| JP6182443B2 (ja) | 架橋ビスインデニル化合物の製造方法 | |
| JP2021507963A (ja) | 担持メタロセン触媒の製造方法およびこれから製造された触媒を用いるポリプロピレンの製造方法 | |
| KR101178996B1 (ko) | 1-헥센 제조용 촉매 및 이를 이용한 1-헥센의 제조방법 | |
| JP2013047198A (ja) | 三座配位子ロジウム錯体、その製造方法、置換アセチレン重合開始剤及びそれを用いた置換ポリアセチレン誘導体の製造方法 | |
| JP2023176740A (ja) | 有機リン化合物の製造方法 | |
| KR20150016828A (ko) | 신규한 리간드 화합물 및 이를 포함하는 전이금속 화합물 |