JP2008545821A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2008545821A5 JP2008545821A5 JP2008512305A JP2008512305A JP2008545821A5 JP 2008545821 A5 JP2008545821 A5 JP 2008545821A5 JP 2008512305 A JP2008512305 A JP 2008512305A JP 2008512305 A JP2008512305 A JP 2008512305A JP 2008545821 A5 JP2008545821 A5 JP 2008545821A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- alkyl
- aryl
- different
- 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.)
- Ceased
Links
- 150000001875 compounds Chemical class 0.000 claims description 24
- 239000003054 catalyst Substances 0.000 claims description 19
- 150000002902 organometallic compounds Chemical class 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 14
- 150000002894 organic compounds Chemical class 0.000 claims description 12
- 239000012876 carrier material Substances 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 11
- 239000002879 Lewis base Substances 0.000 claims description 9
- 150000007527 lewis bases Chemical class 0.000 claims description 9
- 239000007795 chemical reaction product Substances 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 239000000725 suspension Substances 0.000 claims description 4
- 238000006116 polymerization reaction Methods 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 99
- 125000000217 alkyl group Chemical group 0.000 claims 61
- 229910052799 carbon Inorganic materials 0.000 claims 56
- 125000003118 aryl group Chemical group 0.000 claims 53
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 46
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 39
- 238000002360 preparation method Methods 0.000 claims 36
- 238000000034 method Methods 0.000 claims 30
- 125000002877 alkyl aryl group Chemical group 0.000 claims 25
- 125000004122 cyclic group Chemical group 0.000 claims 23
- -1 silanol Chemical group 0.000 claims 20
- 125000003710 aryl alkyl group Chemical group 0.000 claims 19
- 150000002430 hydrocarbons Chemical class 0.000 claims 18
- 229910052739 hydrogen Inorganic materials 0.000 claims 18
- 239000001257 hydrogen Substances 0.000 claims 18
- 125000003342 alkenyl group Chemical group 0.000 claims 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 16
- 125000004104 aryloxy group Chemical group 0.000 claims 15
- 229910052782 aluminium Inorganic materials 0.000 claims 14
- 239000000460 chlorine Substances 0.000 claims 14
- 229910052801 chlorine Inorganic materials 0.000 claims 14
- 125000005842 heteroatom Chemical group 0.000 claims 14
- 229910052710 silicon Inorganic materials 0.000 claims 14
- 229910052757 nitrogen Inorganic materials 0.000 claims 13
- 229910052760 oxygen Inorganic materials 0.000 claims 13
- 229910052698 phosphorus Inorganic materials 0.000 claims 13
- 229910052717 sulfur Inorganic materials 0.000 claims 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 12
- 229910052796 boron Inorganic materials 0.000 claims 12
- 125000003545 alkoxy group Chemical group 0.000 claims 11
- 229910052794 bromium Inorganic materials 0.000 claims 11
- 230000000737 periodic effect Effects 0.000 claims 11
- 125000005103 alkyl silyl group Chemical group 0.000 claims 10
- 125000005104 aryl silyl group Chemical group 0.000 claims 10
- 229910052731 fluorine Inorganic materials 0.000 claims 10
- 125000005843 halogen group Chemical group 0.000 claims 10
- 239000011541 reaction mixture Substances 0.000 claims 10
- 150000001336 alkenes Chemical class 0.000 claims 9
- 125000000524 functional group Chemical group 0.000 claims 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 8
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims 8
- 150000001721 carbon Chemical group 0.000 claims 8
- 229910052726 zirconium Inorganic materials 0.000 claims 8
- 125000001931 aliphatic group Chemical group 0.000 claims 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 7
- 229910052751 metal Inorganic materials 0.000 claims 7
- 239000002184 metal Substances 0.000 claims 7
- 125000005018 aryl alkenyl group Chemical group 0.000 claims 6
- 125000004429 atom Chemical group 0.000 claims 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 6
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims 6
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 6
- 125000001188 haloalkyl group Chemical group 0.000 claims 6
- 125000003106 haloaryl group Chemical group 0.000 claims 6
- 125000002034 haloarylalkyl group Chemical group 0.000 claims 6
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims 6
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 6
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 5
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 5
- 125000006492 halo alkyl aryl group Chemical group 0.000 claims 5
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 5
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 5
- 150000003254 radicals Chemical group 0.000 claims 5
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims 4
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims 4
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 4
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 4
- 229910052735 hafnium Inorganic materials 0.000 claims 4
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 4
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 4
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 4
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims 4
- 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 claims 4
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 4
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims 3
- 239000004215 Carbon black (E152) Substances 0.000 claims 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 3
- 125000003828 azulenyl group Chemical group 0.000 claims 3
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 claims 3
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims 3
- 125000003709 fluoroalkyl group Chemical group 0.000 claims 3
- 238000010438 heat treatment Methods 0.000 claims 3
- 229930195733 hydrocarbon Natural products 0.000 claims 3
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims 3
- 239000011261 inert gas Substances 0.000 claims 3
- ZWRDBWDXRLPESY-UHFFFAOYSA-N n-benzyl-n-ethylethanamine Chemical compound CCN(CC)CC1=CC=CC=C1 ZWRDBWDXRLPESY-UHFFFAOYSA-N 0.000 claims 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 claims 3
- 229940031826 phenolate Drugs 0.000 claims 3
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 2
- 239000005977 Ethylene Substances 0.000 claims 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 2
- 229910052783 alkali metal Inorganic materials 0.000 claims 2
- 150000001340 alkali metals Chemical class 0.000 claims 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 2
- 150000001342 alkaline earth metals Chemical class 0.000 claims 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 2
- 150000005840 aryl radicals Chemical class 0.000 claims 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 claims 2
- MQXCDPDLPMAEIE-UHFFFAOYSA-N bis(2,3,4,5,6-pentafluorophenyl)borinic acid Chemical compound FC=1C(F)=C(F)C(F)=C(F)C=1B(O)C1=C(F)C(F)=C(F)C(F)=C1F MQXCDPDLPMAEIE-UHFFFAOYSA-N 0.000 claims 2
- 238000001035 drying Methods 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
- 229910021478 group 5 element Inorganic materials 0.000 claims 2
- 239000003446 ligand Substances 0.000 claims 2
- 239000000178 monomer Substances 0.000 claims 2
- HVAAHUDGWQAAOJ-UHFFFAOYSA-N n-benzylethanamine Chemical compound CCNCC1=CC=CC=C1 HVAAHUDGWQAAOJ-UHFFFAOYSA-N 0.000 claims 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- 125000002524 organometallic group Chemical group 0.000 claims 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 2
- 239000010703 silicon Substances 0.000 claims 2
- 229910052718 tin Inorganic materials 0.000 claims 2
- 238000005406 washing Methods 0.000 claims 2
- VASOMTXTRMYSKD-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenyl)boronic acid Chemical compound OB(O)C1=C(F)C(F)=C(F)C(F)=C1F VASOMTXTRMYSKD-UHFFFAOYSA-N 0.000 claims 1
- 125000006218 1-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 claims 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 230000003213 activating effect Effects 0.000 claims 1
- 125000005282 allenyl group Chemical group 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- UPABQMWFWCMOFV-UHFFFAOYSA-N benethamine Chemical compound C=1C=CC=CC=1CNCCC1=CC=CC=C1 UPABQMWFWCMOFV-UHFFFAOYSA-N 0.000 claims 1
- 150000001639 boron compounds Chemical class 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000003245 coal Substances 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 238000003379 elimination reaction Methods 0.000 claims 1
- 125000001841 imino group Chemical group [H]N=* 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- LYBKPDDZTNUNNM-UHFFFAOYSA-N isopropylbenzylamine Chemical compound CC(C)NCC1=CC=CC=C1 LYBKPDDZTNUNNM-UHFFFAOYSA-N 0.000 claims 1
- 229910052744 lithium Inorganic materials 0.000 claims 1
- 229910052749 magnesium Inorganic materials 0.000 claims 1
- 239000011777 magnesium Substances 0.000 claims 1
- ZYZHMSJNPCYUTB-UHFFFAOYSA-N n-benzyl-1-phenylethanamine Chemical compound C=1C=CC=CC=1C(C)NCC1=CC=CC=C1 ZYZHMSJNPCYUTB-UHFFFAOYSA-N 0.000 claims 1
- DLSOILHAKCBARI-UHFFFAOYSA-N n-benzyl-2-methylpropan-2-amine Chemical compound CC(C)(C)NCC1=CC=CC=C1 DLSOILHAKCBARI-UHFFFAOYSA-N 0.000 claims 1
- WYZDCUGWXKHESN-UHFFFAOYSA-N n-benzyl-n-methyl-1-phenylmethanamine Chemical compound C=1C=CC=CC=1CN(C)CC1=CC=CC=C1 WYZDCUGWXKHESN-UHFFFAOYSA-N 0.000 claims 1
- HIPXPABRMMYVQD-UHFFFAOYSA-N n-benzylbutan-1-amine Chemical compound CCCCNCC1=CC=CC=C1 HIPXPABRMMYVQD-UHFFFAOYSA-N 0.000 claims 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims 1
- RIWRFSMVIUAEBX-UHFFFAOYSA-N n-methyl-1-phenylmethanamine Chemical compound CNCC1=CC=CC=C1 RIWRFSMVIUAEBX-UHFFFAOYSA-N 0.000 claims 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 230000002018 overexpression Effects 0.000 claims 1
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- 239000002685 polymerization catalyst Substances 0.000 claims 1
- 230000000379 polymerizing effect Effects 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims 1
- 239000000741 silica gel Substances 0.000 claims 1
- 229910002027 silica gel Inorganic materials 0.000 claims 1
- 239000000377 silicon dioxide Substances 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 125000005017 substituted alkenyl group Chemical group 0.000 claims 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 0 CC1=C(*)C(C(*)C(**)C2*C3C4C(*)=C(*)C(*)=C(*)C4C(*)C3*)C2C(*)=C1C Chemical compound CC1=C(*)C(C(*)C(**)C2*C3C4C(*)=C(*)C(*)=C(*)C4C(*)C3*)C2C(*)=C1C 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 1
- 230000037048 polymerization activity Effects 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/130,925 US7232869B2 (en) | 2005-05-17 | 2005-05-17 | Catalyst composition for olefin polymerization |
| PCT/US2006/016114 WO2006124231A1 (en) | 2005-05-17 | 2006-04-27 | Catalyst composition for olefin polymerization |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008545821A JP2008545821A (ja) | 2008-12-18 |
| JP2008545821A5 true JP2008545821A5 (enExample) | 2011-06-23 |
Family
ID=36829739
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008512305A Ceased JP2008545821A (ja) | 2005-05-17 | 2006-04-27 | オレフィン重合用の触媒組成物 |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US7232869B2 (enExample) |
| EP (1) | EP1882000B1 (enExample) |
| JP (1) | JP2008545821A (enExample) |
| KR (1) | KR101190758B1 (enExample) |
| CN (1) | CN101384624B (enExample) |
| AT (1) | ATE462731T1 (enExample) |
| BR (1) | BRPI0610163A2 (enExample) |
| DE (1) | DE602006013300D1 (enExample) |
| ES (1) | ES2342106T3 (enExample) |
| TW (1) | TW200710110A (enExample) |
| WO (1) | WO2006124231A1 (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102005052654A1 (de) * | 2005-11-04 | 2007-05-16 | Ticona Gmbh | Verfahren zur Herstellung von ultrahochmolekularen Polymeren unter Verwendung von speziellen verbrückten Metallocen-Katalysatoren |
| PT2099832T (pt) | 2006-12-14 | 2019-06-27 | Grace W R & Co | Ativadores de catalisador, processos para preparação dos mesmos, e sua utilização em catalisadores e polimerização de olefinas |
| BRPI0722162A2 (pt) | 2007-10-25 | 2014-03-18 | Lummus Novolen Technology Gmbh | Compostos de metaloceno, catalisadores compreendendo os mesmos, processo para produzir um polímero de olefina pelo uso de catalisadores, e homo-e copolímeros de olefina. |
| KR101278336B1 (ko) * | 2007-10-25 | 2013-06-25 | 루머스 노보렌 테크놀로지 게엠베하 | 안사-메탈로센 화합물의 라세모선택적 합성, 안사-메탈로센 화합물, 이를 포함하는 촉매, 그 촉매를 이용한 올레핀 폴리머 제조 공정, 그리고 올레핀 호모- 및 코폴리머 |
| EP2172493A1 (en) | 2008-10-02 | 2010-04-07 | Total Petrochemicals Research Feluy | Activating supports based on perfluorinated boronic acids |
| JP2012513463A (ja) * | 2008-12-31 | 2012-06-14 | ルムス・ノボレン・テクノロジー・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 新たなメタロセン化合物、それを含む触媒、その触媒を使用するオレフィンポリマーの製造プロセス、ならびにオレフィンホモポリマーおよびコポリマー |
| EP2633104A1 (en) | 2010-10-28 | 2013-09-04 | Lummus Novolen Technology Gmbh | Nonwoven and yarn polypropylene with additivation |
| BR112013010627B1 (pt) * | 2010-11-22 | 2020-01-28 | Albemarle Corp | composições de ativador, sua preparação e seu uso em catálise |
| EP2573091A1 (en) | 2011-09-23 | 2013-03-27 | Lummus Novolen Technology Gmbh | Process for recycling of free ligand from their corresponding metallocene complexes |
| WO2013118140A2 (en) * | 2012-02-08 | 2013-08-15 | Reliance Industries Ltd | Immobilization of single site catalyst on inorganic oxide support for preparation of uhmwpe |
| EP2824107B1 (en) | 2012-05-08 | 2017-01-18 | Lg Chem, Ltd. | Ansa-metallocene compound and method for preparing supported catalyst using same |
| KR101584350B1 (ko) * | 2013-04-08 | 2016-01-13 | 한화케미칼 주식회사 | 대전 방지제를 포함하는 메탈로센 촉매 시스템 및 이를 이용한 폴리올레핀의 제조 방법 |
| FR3039431B1 (fr) * | 2015-07-29 | 2019-05-31 | IFP Energies Nouvelles | Nouvelle composition catalytique a base de nickel et d'un ligand de type phosphine complexe au nickel et son utilisation dans un procede d'oligomerisation des olefines |
| FR3042989A1 (fr) * | 2015-10-30 | 2017-05-05 | Ifp Energies Now | Nouvelle composition catalytique a base de nickel en presence d'un activateur specifique et son utilisation dans un procede d'oligomerisation des olefines |
| FR3045414B1 (fr) * | 2015-12-18 | 2019-12-27 | IFP Energies Nouvelles | Nouvelle composition catalytique a base de nickel et de ligand de type phosphine et d'une base de lewis et son utilisation dans un procede d'oligomerisation des olefines |
| CN108786919B (zh) * | 2017-05-05 | 2020-07-21 | 中国石油化工股份有限公司 | 负载型茂金属催化剂及其制备方法和应用和丙烯酸甲酯的制备方法 |
| CN108786918B (zh) * | 2017-05-05 | 2020-07-24 | 中国石油化工股份有限公司 | 负载型茂金属催化剂及其制备方法和应用和丙烯酸甲酯的制备方法 |
| US11161922B2 (en) | 2017-10-31 | 2021-11-02 | Exxonmobil Chemical Patents Inc. | Toluene free silica supported single-site metallocene catalysts from in-situ supported MAO formation in aliphatic solvents |
| WO2019089145A1 (en) | 2017-10-31 | 2019-05-09 | Exxonmobil Chemical Patents Inc. | Toluene free silica supported single-site metallocene catalysts from in-situ supported alumoxane formation in aliphatic solvents |
| KR102301666B1 (ko) * | 2017-12-22 | 2021-09-14 | 주식회사 엘지화학 | 혼성 담지 메탈로센 촉매의 제조 방법, 상기 제조 방법으로 제조된 혼성 담지 메탈로센 촉매, 및 이를 이용하는 폴리올레핀의 제조 방법 |
| KR102431269B1 (ko) | 2018-11-02 | 2022-08-10 | 주식회사 엘지화학 | 신규 전이금속 화합물 및 이를 이용한 폴리프로필렌의 제조방법 |
| US11352375B2 (en) | 2018-12-28 | 2022-06-07 | Braskem S.A. | Auxiliaries for olefin polymerization process |
| US11866522B2 (en) | 2018-12-28 | 2024-01-09 | Braskem S.A. | Process for introducing catalyst in a polymerization process |
| CN115368490B (zh) * | 2021-05-20 | 2023-11-28 | 中国科学技术大学 | 硼烷助催化剂、合成方法及其应用 |
| CN121021585A (zh) * | 2025-10-28 | 2025-11-28 | 洛阳常龙新材料科技有限公司 | 一种第一代Grubbs催化剂的制备方法 |
Family Cites Families (102)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3127133A1 (de) * | 1981-07-09 | 1983-01-27 | Hoechst Ag, 6000 Frankfurt | Verfahren zur herstellung von polyolefinen und deren copolymerisaten |
| US4530914A (en) * | 1983-06-06 | 1985-07-23 | Exxon Research & Engineering Co. | Process and catalyst for producing polyethylene having a broad molecular weight distribution |
| US5324800A (en) * | 1983-06-06 | 1994-06-28 | Exxon Chemical Patents Inc. | Process and catalyst for polyolefin density and molecular weight control |
| US4937299A (en) * | 1983-06-06 | 1990-06-26 | Exxon Research & Engineering Company | Process and catalyst for producing reactor blend polyolefins |
| ZA844157B (en) | 1983-06-06 | 1986-01-29 | Exxon Research Engineering Co | Process and catalyst for polyolefin density and molecular weight control |
| DE3508887A1 (de) * | 1985-03-13 | 1986-09-25 | Hoechst Ag, 6230 Frankfurt | Verfahren zur herstellung von optisch aktiven polyolefinen |
| US4808561A (en) * | 1985-06-21 | 1989-02-28 | Exxon Chemical Patents Inc. | Supported polymerization catalyst |
| US4752597A (en) * | 1985-12-12 | 1988-06-21 | Exxon Chemical Patents Inc. | New polymerization catalyst |
| PL276385A1 (en) * | 1987-01-30 | 1989-07-24 | Exxon Chemical Patents Inc | Method for polymerization of olefines,diolefins and acetylene unsaturated compounds |
| US5384299A (en) * | 1987-01-30 | 1995-01-24 | Exxon Chemical Patents Inc. | Ionic metallocene catalyst compositions |
| US5198401A (en) * | 1987-01-30 | 1993-03-30 | Exxon Chemical Patents Inc. | Ionic metallocene catalyst compositions |
| ES2082745T3 (es) | 1987-04-03 | 1996-04-01 | Fina Technology | Sistemas cataliticos metalocenos para la polimerizacion de las olefinas presentando un puente de hidrocarburo de silicio. |
| DE3726067A1 (de) * | 1987-08-06 | 1989-02-16 | Hoechst Ag | Verfahren zur herstellung von 1-olefinpolymeren |
| US4931417A (en) * | 1987-11-09 | 1990-06-05 | Chisso Corporation | Transition-metal compound having a bis-substituted-cyclopentadienyl ligand of bridged structure |
| DE3742934A1 (de) | 1987-12-18 | 1989-06-29 | Hoechst Ag | Verfahren zur herstellung einer chiralen, stereorigiden metallocen-verbindung |
| DE3808268A1 (de) * | 1988-03-12 | 1989-09-21 | Hoechst Ag | Verfahren zur herstellung eines 1-olefinpolymers |
| US5120867A (en) * | 1988-03-21 | 1992-06-09 | Welborn Jr Howard C | Silicon-bridged transition metal compounds |
| US5017714A (en) * | 1988-03-21 | 1991-05-21 | Exxon Chemical Patents Inc. | Silicon-bridged transition metal compounds |
| US4871705A (en) * | 1988-06-16 | 1989-10-03 | Exxon Chemical Patents Inc. | Process for production of a high molecular weight ethylene a-olefin elastomer with a metallocene alumoxane catalyst |
| DE3907964A1 (de) * | 1989-03-11 | 1990-09-13 | Hoechst Ag | Verfahren zur herstellung eines syndiotaktischen polyolefins |
| 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 |
| US5057475A (en) * | 1989-09-13 | 1991-10-15 | Exxon Chemical Patents Inc. | Mono-Cp heteroatom containing group IVB transition metal complexes with MAO: supported catalyst for olefin polymerization |
| 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 |
| US5243001A (en) * | 1990-11-12 | 1993-09-07 | Hoechst Aktiengesellschaft | Process for the preparation of a high molecular weight olefin polymer |
| US5239022A (en) * | 1990-11-12 | 1993-08-24 | Hoechst Aktiengesellschaft | Process for the preparation of a syndiotactic polyolefin |
| EP0485823B1 (de) * | 1990-11-12 | 1995-03-08 | Hoechst Aktiengesellschaft | 2-Substituierte Bisindenylmetallocene, Verfahren zu ihrer Herstellung und ihre Verwendung als Katalysatoren bei der Olefinpolymerisation |
| ES2090209T3 (es) * | 1990-11-12 | 1996-10-16 | Hoechst Ag | Metalocenos con ligandos basados en derivados de indenilo sustituidos en posicion 2, procedimiento para su preparacion y su empleo como catalizadores. |
| US5436305A (en) * | 1991-05-09 | 1995-07-25 | Phillips Petroleum Company | Organometallic fluorenyl compounds, preparation, and use |
| DE4120009A1 (de) * | 1991-06-18 | 1992-12-24 | Basf Ag | Loesliche katalysatorsysteme zur herstellung von polyalk-1-enen mit hohen molmassen |
| TW300901B (enExample) * | 1991-08-26 | 1997-03-21 | Hoechst Ag | |
| ATE286918T1 (de) * | 1991-10-15 | 2005-01-15 | Basell Polyolefine Gmbh | Verfahren zur herstellung eines olefinpolymers unter verwendung von metallocenen mit speziell substituierten indenylliganden |
| JP3371118B2 (ja) * | 1991-11-30 | 2003-01-27 | バーゼル・ポリオレフィン・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | 配位子としてベンゼン融合したインデニル誘導体を持つメタロセン、その製造方法および触媒としてのその用途 |
| US5830821A (en) * | 1991-11-30 | 1998-11-03 | Targor Gmbh | Process for olefin preparation using metallocenes having benzo-fused indenyl derivatives as ligands |
| TW318184B (enExample) * | 1991-11-30 | 1997-10-21 | Hoechst Ag | |
| US5932669A (en) * | 1991-11-30 | 1999-08-03 | Targor Gmbh | Metallocenes having benzo-fused indenyl derivatives as ligands, processes for their preparation and their use as catalysts |
| TW309523B (enExample) * | 1991-11-30 | 1997-07-01 | Hoechst Ag | |
| US5350723A (en) * | 1992-05-15 | 1994-09-27 | The Dow Chemical Company | Process for preparation of monocyclopentadienyl metal complex compounds and method of use |
| US5240894A (en) * | 1992-05-18 | 1993-08-31 | Exxon Chemical Patents Inc. | Method for making and using a supported metallocene catalyst system |
| DE69224184T2 (de) * | 1992-06-13 | 1999-06-02 | Targor GmbH, 55116 Mainz | Verfahren zur Herstellung von verbrückten, chiralen Metallocenkatalysatoren des Types Bisindenyl |
| TW294669B (enExample) | 1992-06-27 | 1997-01-01 | Hoechst Ag | |
| EP0584609B1 (de) * | 1992-08-15 | 1999-03-10 | TARGOR GmbH | Verfahren zur Herstellung von Polyolefinen |
| US5332706A (en) | 1992-12-28 | 1994-07-26 | Mobil Oil Corporation | Process and a catalyst for preventing reactor fouling |
| JP3307704B2 (ja) * | 1993-02-19 | 2002-07-24 | 三菱化学株式会社 | α‐オレフィン重合体の製造法 |
| JP3293927B2 (ja) | 1993-02-19 | 2002-06-17 | 三菱化学株式会社 | α‐オレフィン重合用触媒成分およびそれを用いたα‐オレフィン重合体の製造法 |
| DE69408989T2 (de) | 1993-05-25 | 1998-11-05 | Exxon Chemical Patents Inc | Metallocen-katalysatorsysteme auf einem träger für die olefinpolymerisation, ihre herstellung und verwendung |
| EP1209165B1 (en) * | 1993-06-07 | 2006-04-19 | Mitsui Chemicals, Inc. | Propylene elastomer |
| EP1070729B1 (en) * | 1993-06-07 | 2011-09-28 | Mitsui Chemicals, Inc. | Transition metal compound, olefin polymerization catalyst component comprising said compound, olefin polymerization catalyst containing said component, process for olefin polymerization using said catalyst, propylene homopolymer, propylene copolymer and propylene elastomer |
| JP3423378B2 (ja) * | 1993-11-12 | 2003-07-07 | 三井化学株式会社 | 新規な遷移金属化合物および該遷移金属化合物からなるオレフィン重合用触媒成分、該オレフィン重合用触媒成分を含むオレフィン重合用触媒ならびにオレフィンの重合方法 |
| DE4344689A1 (de) * | 1993-12-27 | 1995-06-29 | Hoechst Ag | Metallocenverbindung |
| DE4344688A1 (de) * | 1993-12-27 | 1995-06-29 | Hoechst Ag | Metallocenverbindung |
| DE4406109A1 (de) | 1994-02-25 | 1995-08-31 | Witco Gmbh | Verfahren zur Herstellung von verbrückten stereorigiden Metallocenen |
| BR9508119A (pt) * | 1994-06-24 | 1997-08-12 | Exxon Chemical Patents Inc | Sistemas de catalisador de polimerização produção e uso dos mesmos |
| ES2164774T3 (es) | 1994-08-03 | 2002-03-01 | Exxonmobil Chem Patents Inc | Composicion catalitica ionica soportada. |
| US6140432A (en) * | 1995-07-13 | 2000-10-31 | Exxon Chemical Patents Inc. | Polymerization catalyst systems, their production and use |
| US6124230A (en) * | 1995-07-13 | 2000-09-26 | Exxon Chemical Patents, Inc. | Polymerization catalyst systems, their production and use |
| US5939347A (en) | 1995-01-25 | 1999-08-17 | W.R. Grace & Co. -Conn. | Supported catalytic activator |
| US5635437A (en) * | 1995-07-28 | 1997-06-03 | Exxon Chemicals Patents, Inc. | Method for preparing metallocene catalyst systems |
| DE19544828A1 (de) * | 1995-12-01 | 1997-06-05 | Hoechst Ag | Hochmolekulare Copolymere |
| US5678812A (en) * | 1996-02-14 | 1997-10-21 | R. R. Donnelley & Sons Company | Bindery apparatus with gathering conveyors and a method of make-ready |
| CN1214055A (zh) | 1996-03-04 | 1999-04-14 | 埃克森化学专利公司 | 稳定的金属茂催化剂体系 |
| HU223533B1 (hu) * | 1996-06-17 | 2004-08-30 | Exxonmobil Chemical Patents Inc. | Vegyes átmenetifém katalizátor-rendszer olefinek polimerizálására |
| WO1998001481A1 (de) | 1996-07-04 | 1998-01-15 | Basf Aktiengesellschaft | Verfahren zur herstellung von geträgerten übergangsmetallkatalysatoren |
| KR100536794B1 (ko) | 1996-11-15 | 2005-12-14 | 바셀 테크놀로지 캄파니 비이브이 | 복소환 메탈로센 및 중합 촉매 |
| EP0846696B1 (en) * | 1996-12-09 | 2003-06-18 | Mitsubishi Chemical Corporation | Catalyst for polymerization of alpha-olefins |
| EP0985674B1 (en) * | 1997-01-21 | 2003-04-23 | Mitsubishi Chemical Corporation | Organic compounds containing silicon or germanium, transition metal complexes, catalyst for alpha-olefin polymerization, and processes for producing alpha-olefin polymers |
| DE19757563A1 (de) * | 1997-03-07 | 1999-07-08 | Targor Gmbh | Geträgertes Katalysatorsystem, Verfahren zur Herstellung und seine Verwendung zur Polymerisation von Olefinen |
| US6228795B1 (en) * | 1997-06-05 | 2001-05-08 | Exxon Chemical Patents, Inc. | Polymeric supported catalysts |
| EP0986586B1 (en) * | 1997-06-05 | 2008-06-18 | ExxonMobil Chemical Patents Inc. | Polymeric supported catalysts for olefin polymerization |
| DE19733017A1 (de) * | 1997-07-31 | 1999-02-04 | Hoechst Ag | Chemische Verbindung |
| DE19757540A1 (de) | 1997-12-23 | 1999-06-24 | Hoechst Ag | Geträgertes Katalysatorsystem zur Polymerisation von Olefinen |
| DE19804970A1 (de) | 1998-02-07 | 1999-08-12 | Aventis Res & Tech Gmbh & Co | Katalysatorsystem |
| 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 |
| DE19833170A1 (de) | 1998-07-23 | 2000-01-27 | Targor Gmbh | Verfahren zur Herstellung eines metallhaltigen Trägerkatalysators oder einer Trägerkatalysatorkomponente durch Tränkung einer Trägersubstanz |
| CN1142190C (zh) | 1998-08-26 | 2004-03-17 | 埃克森化学专利公司 | 高活性负载型催化剂组合物 |
| DE19903306A1 (de) * | 1999-01-28 | 2000-08-03 | Targor Gmbh | Organometallverbindung, Katalysatorsystem enthaltend diese Organometallverbindung und seine Verwendung |
| DE19917985A1 (de) | 1999-04-21 | 2000-10-26 | Targor Gmbh | Katalysatorsystem |
| DE19962814A1 (de) | 1999-12-23 | 2001-06-28 | Targor Gmbh | Neues Katalysatorsystem und dessen Verwendung |
| US7342078B2 (en) | 1999-12-23 | 2008-03-11 | Basell Polyolefine Gmbh | Transition metal compound, ligand system, catalyst system and the use of the latter for polymerisation and copolymerisation of olefins |
| US6376412B1 (en) * | 2000-06-30 | 2002-04-23 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6376413B1 (en) * | 2000-06-30 | 2002-04-23 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6380120B1 (en) * | 2000-06-30 | 2002-04-30 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6376407B1 (en) * | 2000-06-30 | 2002-04-23 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6380334B1 (en) * | 2000-06-30 | 2002-04-30 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6376408B1 (en) * | 2000-06-30 | 2002-04-23 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6380123B1 (en) * | 2000-06-30 | 2002-04-30 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6380124B1 (en) * | 2000-06-30 | 2002-04-30 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6380331B1 (en) * | 2000-06-30 | 2002-04-30 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6380122B1 (en) * | 2000-06-30 | 2002-04-30 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6376411B1 (en) * | 2000-06-30 | 2002-04-23 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6380330B1 (en) * | 2000-06-30 | 2002-04-30 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6376409B1 (en) * | 2000-06-30 | 2002-04-23 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6376627B1 (en) * | 2000-06-30 | 2002-04-23 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6376410B1 (en) * | 2000-06-30 | 2002-04-23 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6399723B1 (en) * | 2000-06-30 | 2002-06-04 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6380121B1 (en) * | 2000-06-30 | 2002-04-30 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| SG96700A1 (en) * | 2001-09-27 | 2003-06-16 | Sumitomo Chemical Co | Catalyst component for addition polymerization, process for producing catalyst for addition polymerization and process for producing addition polymer |
| ES2268126T3 (es) | 2001-11-30 | 2007-03-16 | Basell Polyolefine Gmbh | Compuestos de metaloceno y procedimiento para la preparacion de polimeros de propileno. |
| EP1511755B1 (en) | 2002-06-12 | 2006-03-08 | Basell Polyolefine GmbH | Transition metal compounds their preparation and their use in catalyst systems for the polymerization and copolymerization of olefins |
| US7285513B2 (en) * | 2002-07-15 | 2007-10-23 | Basell Polyolefine Gmbh | Preparation of catalyst systems |
| JP2005538245A (ja) | 2002-07-15 | 2005-12-15 | バーゼル、ポリオレフィン、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツング | 担体を有する触媒組成物の製造方法 |
| SG130016A1 (en) * | 2002-09-24 | 2007-03-20 | Sumitomo Chemical Co | Modified particle, catalyst component for addition polymerization, catalyst for addition polymerization and process for producing addition polymer |
| US7592402B2 (en) * | 2004-04-30 | 2009-09-22 | Sumitomo Chemical Company, Limited | Process for producing modified particle; carrier; catalyst component for addition polymerization; process for producing catalyst for addition polymerization; and process for producing addition polymer |
-
2005
- 2005-05-17 US US11/130,925 patent/US7232869B2/en not_active Expired - Fee Related
-
2006
- 2006-04-27 DE DE602006013300T patent/DE602006013300D1/de active Active
- 2006-04-27 EP EP06758705A patent/EP1882000B1/en not_active Not-in-force
- 2006-04-27 JP JP2008512305A patent/JP2008545821A/ja not_active Ceased
- 2006-04-27 CN CN2006800169691A patent/CN101384624B/zh not_active Expired - Fee Related
- 2006-04-27 WO PCT/US2006/016114 patent/WO2006124231A1/en not_active Ceased
- 2006-04-27 KR KR1020077029523A patent/KR101190758B1/ko not_active Expired - Fee Related
- 2006-04-27 BR BRPI0610163-1A patent/BRPI0610163A2/pt not_active IP Right Cessation
- 2006-04-27 ES ES06758705T patent/ES2342106T3/es active Active
- 2006-04-27 AT AT06758705T patent/ATE462731T1/de active
- 2006-05-04 TW TW095115912A patent/TW200710110A/zh unknown
-
2007
- 2007-05-16 US US11/803,801 patent/US7468416B2/en not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2008545821A5 (enExample) | ||
| JP6420911B2 (ja) | 混成担持触媒およびこれを用いるオレフィン系重合体の製造方法 | |
| CN1049899C (zh) | 烯烃的聚合方法 | |
| JP6282341B2 (ja) | 混成担持メタロセン触媒 | |
| JP6247751B2 (ja) | 混成担持メタロセン触媒の製造方法 | |
| CN105358589B (zh) | 金属茂和由其衍生的催化剂组合物 | |
| CN107849079B (zh) | 茂金属化合物及其制备方法 | |
| TWI280252B (en) | Polymerization catalyst activators, method of preparing, and their use in polymerization processes | |
| WO1995009172A1 (en) | Transition metal compound, olefin polymerization catalyst, and process for producing olefin polymer by using said catalyst | |
| US8163854B2 (en) | Preparation of supported silyl-capped silica-bound anion activators and associated catalysts | |
| KR20130056247A (ko) | 알킬 시클로펜타디엔 화합물의 합성 | |
| CN111527112B (zh) | 负载型茂金属催化剂的制备方法及使用由此制备的催化剂制备聚丙烯的方法 | |
| JP2017160196A5 (enExample) | ||
| CN102190749B (zh) | 一种乙烯/α-烯烃共聚合的方法 | |
| CN105985463B (zh) | 一种桥联型茂金属化合物催化剂、其制备方法及其应用 | |
| JP3743687B2 (ja) | ハロゲン化アルキルを用いるテトラキス（ペンタフルオロフェニル）ボレート誘導体の製造方法 | |
| CN102666604A (zh) | 单活性中心催化剂的制备 | |
| CN112661893A (zh) | 一种乙烯与环烯烃共聚用主催化剂及其聚合方法与应用 | |
| CN1491235A (zh) | 作为催化剂组分的过渡金属化合物及其在生产聚烯烃中的用途 | |
| CN111556878A (zh) | 负载型茂金属催化剂和使用该催化剂制备聚丙烯的方法 | |
| JP2016506979A (ja) | 改善した流動を有する触媒組成物を作製するためのプロセス | |
| KR102024327B1 (ko) | 메탈로센 화합물, 이를 포함하는 촉매 조성물 및 이를 이용한 올레핀 중합체의 제조방법 | |
| JP2014511910A (ja) | ビニル末端高級オレフィンコポリマーおよびその生成方法 | |
| CN103665051B (zh) | 单茂金属化合物及其在间规聚苯乙烯催化聚合中的应用 | |
| KR101293419B1 (ko) | 구경꾼 리간드를 포함하는 금속-유기 화합물의 제조방법 |