JP2004505019A5 - - Google Patents
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- Publication number
- JP2004505019A5 JP2004505019A5 JP2002507829A JP2002507829A JP2004505019A5 JP 2004505019 A5 JP2004505019 A5 JP 2004505019A5 JP 2002507829 A JP2002507829 A JP 2002507829A JP 2002507829 A JP2002507829 A JP 2002507829A JP 2004505019 A5 JP2004505019 A5 JP 2004505019A5
- Authority
- JP
- Japan
- Prior art keywords
- hydrocarbyl
- dimethyl
- dihydrodibenzo
- azulen
- hydrogen
- 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
- 125000001183 hydrocarbyl group Chemical group 0.000 description 51
- -1 hydrocarbyloxy Chemical group 0.000 description 26
- 229910052739 hydrogen Inorganic materials 0.000 description 18
- 239000001257 hydrogen Substances 0.000 description 18
- 125000004429 atom Chemical group 0.000 description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 7
- 150000002431 hydrogen Chemical class 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 150000004820 halides Chemical class 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- FVZVCSNXTFCBQU-UHFFFAOYSA-N phosphanyl Chemical group [PH2] FVZVCSNXTFCBQU-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 3
- 150000004696 coordination complex Chemical class 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 150000001350 alkyl halides Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 150000001502 aryl halides Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- FFIMZWXRPYQJNC-UHFFFAOYSA-N C1(=CC=CC=C1)C=CC=CC1=CC=CC=C1.[Ti+2].CN([SiH]=O)C Chemical compound C1(=CC=CC=C1)C=CC=CC1=CC=CC=C1.[Ti+2].CN([SiH]=O)C FFIMZWXRPYQJNC-UHFFFAOYSA-N 0.000 description 1
- QFZJXZKYWZNYRA-UHFFFAOYSA-N C=CC=CC.[Ti+2].[SiH](=O)N(C)C Chemical compound C=CC=CC.[Ti+2].[SiH](=O)N(C)C QFZJXZKYWZNYRA-UHFFFAOYSA-N 0.000 description 1
- WURFPZILSSYUSY-UHFFFAOYSA-N CC(C)(C)N([SiH]=O)[Ti](C)(C)C(C=C1C2=C(C3)C=CC=C2)C=C1C1=C3C=CC=C1.Cl.Cl Chemical compound CC(C)(C)N([SiH]=O)[Ti](C)(C)C(C=C1C2=C(C3)C=CC=C2)C=C1C1=C3C=CC=C1.Cl.Cl WURFPZILSSYUSY-UHFFFAOYSA-N 0.000 description 1
- BGPKOXZSIZKGNY-UHFFFAOYSA-N CC(C)(C)N([SiH]=O)[Ti](C)(C)C(CC=C1C2=C(C3)C=CC=C2)=C1C1=C3C=CC=C1.Cl.Cl Chemical compound CC(C)(C)N([SiH]=O)[Ti](C)(C)C(CC=C1C2=C(C3)C=CC=C2)=C1C1=C3C=CC=C1.Cl.Cl BGPKOXZSIZKGNY-UHFFFAOYSA-N 0.000 description 1
- UNYYOYPNCPWUOQ-UHFFFAOYSA-N C[Ti](C)(C(CC=C1C2=C(C3)C=CC=C2)=C1C1=C3C=CC=C1)N(C1CCCCC1)[SiH]=O.Cl.Cl Chemical compound C[Ti](C)(C(CC=C1C2=C(C3)C=CC=C2)=C1C1=C3C=CC=C1)N(C1CCCCC1)[SiH]=O.Cl.Cl UNYYOYPNCPWUOQ-UHFFFAOYSA-N 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
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000001588 azulen-1-yl group Chemical group [H]C1=C([H])C2=C([H])C([H])=C([H])C([H])=C([H])C2=C1* 0.000 description 1
- 125000003112 azulen-2-yl group Chemical group [H]C1=C2C([H])=C([H])C([H])=C([H])C([H])=C2C([H])=C1* 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000001993 dienes Chemical group 0.000 description 1
- 238000012685 gas phase polymerization Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 229910052747 lanthanoid Inorganic materials 0.000 description 1
- 150000002602 lanthanoids Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US21545600P | 2000-06-30 | 2000-06-30 | |
| US60/215,456 | 2000-06-30 | ||
| PCT/US2001/018808 WO2002002577A1 (en) | 2000-06-30 | 2001-06-12 | Polycyclic, fused ring compounds, metal complexes and polymerization process |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004505019A JP2004505019A (ja) | 2004-02-19 |
| JP2004505019A5 true JP2004505019A5 (enExample) | 2008-07-31 |
| JP4964389B2 JP4964389B2 (ja) | 2012-06-27 |
Family
ID=22803050
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002507829A Expired - Lifetime JP4964389B2 (ja) | 2000-06-30 | 2001-06-12 | 多環式、縮合環化合物、金属錯体及び重合方法 |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US6613921B2 (enExample) |
| EP (1) | EP1299405B1 (enExample) |
| JP (1) | JP4964389B2 (enExample) |
| KR (1) | KR20030013479A (enExample) |
| AT (1) | ATE431353T1 (enExample) |
| AU (1) | AU2001275462A1 (enExample) |
| CA (1) | CA2411712C (enExample) |
| DE (1) | DE60138708D1 (enExample) |
| WO (1) | WO2002002577A1 (enExample) |
Families Citing this family (68)
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| JP7096236B2 (ja) | 2016-09-30 | 2022-07-05 | ダウ グローバル テクノロジーズ エルエルシー | チェーンシャトリングに有用なマルチヘッドまたはデュアルヘッド組成物、およびそれを調製するプロセス |
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| JP2020510129A (ja) | 2017-03-15 | 2020-04-02 | ダウ グローバル テクノロジーズ エルエルシー | マルチブロックコポリマー形成用触媒系 |
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| IT1290856B1 (it) | 1996-12-19 | 1998-12-14 | Enichem Spa | Metalloceni, loro preparazione ed uso nella polimerizzazione di alfa-olefine |
| WO1998031690A1 (fr) | 1997-01-21 | 1998-07-23 | Mitsubishi Chemical Corporation | COMPOSES ORGANIQUES CONTENANT DU SILICIUM OU DU GERMANIUM COMPLEXES DE METAUX DE TRANSITION, CATALYSEUR DE POLYMERISATION D'α-OLEFINE, ET PROCEDES DE PRODUCTION DE POLYMERES D'α-OLEFINE |
| FI972946A7 (fi) | 1997-07-11 | 1999-01-12 | Borealis As | Uudet metalloseeniyhdisteet etyleenisesti tyydyttämättömien monomeerien polymeroimiseksi |
| US6150297A (en) * | 1997-09-15 | 2000-11-21 | The Dow Chemical Company | Cyclopentaphenanthrenyl metal complexes and polymerization process |
| TW490470B (en) | 1998-03-26 | 2002-06-11 | Idemitsu Petrochemical Co | Transition metal compound, polymerization catalyst comprising it, and method for producing polymers using the polymerization catalyst |
| JPH11335387A (ja) * | 1998-03-26 | 1999-12-07 | Idemitsu Petrochem Co Ltd | 遷移金属化合物、それを用いた重合用触媒及び該重合用触媒を用いた重合体の製造方法 |
| JP4116148B2 (ja) | 1998-06-08 | 2008-07-09 | 三菱化学株式会社 | 新規な遷移金属化合物、オレフィン重合用触媒成分およびα−オレフィン重合体の製造方法 |
| AU1270500A (en) * | 1998-11-18 | 2000-06-05 | Montell Technology Company B.V. | Bis(tetrahydro-indenyl) metallocenes as olefin-polymerisation-catalyst |
| DE19916837A1 (de) | 1999-04-14 | 2000-10-19 | Merck Patent Gmbh | Dibenzoazulenderivate |
| IT1318436B1 (it) * | 2000-03-31 | 2003-08-25 | Enichem Spa | Ciclopentadieni sostituiti policiclici e metodo per la loropreparazione. |
| CA2411712C (en) * | 2000-06-30 | 2011-01-25 | Dow Global Technologies Inc. | Polycyclic, fused ring compounds, metal complexes and polymerization process |
-
2001
- 2001-06-12 CA CA2411712A patent/CA2411712C/en not_active Expired - Fee Related
- 2001-06-12 JP JP2002507829A patent/JP4964389B2/ja not_active Expired - Lifetime
- 2001-06-12 AU AU2001275462A patent/AU2001275462A1/en not_active Abandoned
- 2001-06-12 WO PCT/US2001/018808 patent/WO2002002577A1/en not_active Ceased
- 2001-06-12 EP EP01942174A patent/EP1299405B1/en not_active Expired - Lifetime
- 2001-06-12 KR KR1020027018046A patent/KR20030013479A/ko not_active Ceased
- 2001-06-12 US US09/879,463 patent/US6613921B2/en not_active Expired - Lifetime
- 2001-06-12 AT AT01942174T patent/ATE431353T1/de not_active IP Right Cessation
- 2001-06-12 DE DE60138708T patent/DE60138708D1/de not_active Expired - Lifetime
-
2003
- 2003-05-13 US US10/437,161 patent/US6800701B2/en not_active Expired - Lifetime
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