JP2001516367A - メタロセン化合物の製造方法 - Google Patents
メタロセン化合物の製造方法Info
- Publication number
- JP2001516367A JP2001516367A JP53674499A JP53674499A JP2001516367A JP 2001516367 A JP2001516367 A JP 2001516367A JP 53674499 A JP53674499 A JP 53674499A JP 53674499 A JP53674499 A JP 53674499A JP 2001516367 A JP2001516367 A JP 2001516367A
- Authority
- JP
- Japan
- Prior art keywords
- group
- methyl
- butyl
- alkyl
- indenyl
- 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 title claims description 25
- 238000004519 manufacturing process Methods 0.000 title claims description 11
- 238000000034 method Methods 0.000 claims abstract description 51
- 239000003446 ligand Substances 0.000 claims abstract description 18
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims abstract description 13
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 9
- 125000003118 aryl group Chemical group 0.000 claims abstract description 8
- 239000001257 hydrogen Substances 0.000 claims abstract description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 8
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 8
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 7
- 229910052732 germanium Inorganic materials 0.000 claims abstract description 7
- 125000002877 alkyl aryl group Chemical group 0.000 claims abstract description 6
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 6
- 150000002367 halogens Chemical class 0.000 claims abstract description 6
- 150000001342 alkaline earth metals Chemical class 0.000 claims abstract description 5
- 150000003624 transition metals Chemical class 0.000 claims abstract description 5
- 229910052723 transition metal Inorganic materials 0.000 claims abstract description 4
- 229910052747 lanthanoid Inorganic materials 0.000 claims abstract description 3
- 150000002602 lanthanoids Chemical class 0.000 claims abstract description 3
- -1 Pentadienyl Chemical group 0.000 claims description 43
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 28
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 27
- 238000006243 chemical reaction Methods 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 18
- 239000011541 reaction mixture Substances 0.000 claims description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 13
- 229910052751 metal Inorganic materials 0.000 claims description 13
- 239000002184 metal Substances 0.000 claims description 13
- 125000001424 substituent group Chemical group 0.000 claims description 12
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims description 11
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 10
- 229920006395 saturated elastomer Polymers 0.000 claims description 10
- 239000000010 aprotic solvent Substances 0.000 claims description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 9
- 229910052726 zirconium Inorganic materials 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 7
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 7
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 6
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims description 6
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 230000003647 oxidation Effects 0.000 claims description 6
- 238000007254 oxidation reaction Methods 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 5
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000001340 alkali metals Chemical group 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229910052735 hafnium Inorganic materials 0.000 claims description 3
- 230000000737 periodic effect Effects 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 1
- 230000007935 neutral effect Effects 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 abstract description 15
- 230000015572 biosynthetic process Effects 0.000 abstract description 14
- 125000000217 alkyl group Chemical group 0.000 abstract description 8
- 239000003513 alkali Substances 0.000 abstract description 4
- 125000000753 cycloalkyl group Chemical group 0.000 abstract description 4
- 150000002430 hydrocarbons Chemical group 0.000 abstract description 4
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 3
- 229930195733 hydrocarbon Natural products 0.000 abstract description 3
- 150000001255 actinides Chemical group 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 31
- 239000007787 solid Substances 0.000 description 18
- IHLVCKWPAMTVTG-UHFFFAOYSA-N lithium;carbanide Chemical compound [Li+].[CH3-] IHLVCKWPAMTVTG-UHFFFAOYSA-N 0.000 description 12
- 239000000725 suspension Substances 0.000 description 10
- 241000349731 Afzelia bipindensis Species 0.000 description 9
- 238000005160 1H NMR spectroscopy Methods 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 8
- 239000000706 filtrate Substances 0.000 description 8
- 150000001336 alkenes Chemical class 0.000 description 7
- 238000004458 analytical method Methods 0.000 description 7
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 229910007926 ZrCl Inorganic materials 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 6
- 239000000460 chlorine Substances 0.000 description 6
- 239000002168 alkylating agent Substances 0.000 description 5
- 229940100198 alkylating agent Drugs 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- 239000007983 Tris buffer Substances 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 125000002524 organometallic group Chemical group 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- AQZWEFBJYQSQEH-UHFFFAOYSA-N 2-methyloxaluminane Chemical group C[Al]1CCCCO1 AQZWEFBJYQSQEH-UHFFFAOYSA-N 0.000 description 2
- IPBTZXODRJJQBJ-UHFFFAOYSA-N 3-tert-butyl-1-[(3-tert-butyl-1h-inden-1-yl)methyl]-1h-indene Chemical compound C12=CC=CC=C2C(C(C)(C)C)=CC1CC1C2=CC=CC=C2C(C(C)(C)C)=C1 IPBTZXODRJJQBJ-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- 125000005915 C6-C14 aryl group Chemical group 0.000 description 2
- 239000007818 Grignard reagent Substances 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- UHOVQNZJYSORNB-MZWXYZOWSA-N benzene-d6 Chemical compound [2H]C1=C([2H])C([2H])=C([2H])C([2H])=C1[2H] UHOVQNZJYSORNB-MZWXYZOWSA-N 0.000 description 2
- 239000003426 co-catalyst Substances 0.000 description 2
- 150000004696 coordination complex Chemical class 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 150000004795 grignard reagents Chemical class 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000006384 oligomerization reaction Methods 0.000 description 2
- 238000005580 one pot reaction Methods 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000010561 standard procedure Methods 0.000 description 2
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 2
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 2
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 1
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- WAADRLKGQPOVGL-UHFFFAOYSA-N 1-[1-(1h-inden-1-yl)ethyl]-1h-indene Chemical compound C1=CC2=CC=CC=C2C1C(C)C1C2=CC=CC=C2C=C1 WAADRLKGQPOVGL-UHFFFAOYSA-N 0.000 description 1
- PALFTCLHKGGKDW-UHFFFAOYSA-N 1-[2-(1h-inden-1-yl)propan-2-yl]-1h-indene Chemical compound C1=CC2=CC=CC=C2C1C(C)(C)C1C2=CC=CC=C2C=C1 PALFTCLHKGGKDW-UHFFFAOYSA-N 0.000 description 1
- GCZYAOLYVIHWLC-UHFFFAOYSA-N 1-[2-(4,7-dimethyl-1h-inden-1-yl)ethyl]-4,7-dimethyl-1h-indene Chemical compound C1=CC(C(=CC=C2C)C)=C2C1CCC1C(C(C)=CC=C2C)=C2C=C1 GCZYAOLYVIHWLC-UHFFFAOYSA-N 0.000 description 1
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- TZJOVIGBJZKXOE-UHFFFAOYSA-N 2,3,4-trimethylcyclopenta[b]pyrrole Chemical compound N1=C(C)C(C)=C2C(C)=CC=C21 TZJOVIGBJZKXOE-UHFFFAOYSA-N 0.000 description 1
- ZMZGFLUUZLELNE-UHFFFAOYSA-N 2,3,5-triiodobenzoic acid Chemical compound OC(=O)C1=CC(I)=CC(I)=C1I ZMZGFLUUZLELNE-UHFFFAOYSA-N 0.000 description 1
- USVQDQRLYYGLPV-UHFFFAOYSA-N 2-(2,4,4-trimethylpentyl)oxaluminane Chemical compound CC(C)(C)CC(C)C[Al]1CCCCO1 USVQDQRLYYGLPV-UHFFFAOYSA-N 0.000 description 1
- FSWNZCWHTXTQBY-UHFFFAOYSA-N 4,6-dimethylhept-1-ene Chemical compound CC(C)CC(C)CC=C FSWNZCWHTXTQBY-UHFFFAOYSA-N 0.000 description 1
- 239000007848 Bronsted acid Substances 0.000 description 1
- OGFJLWUKRCOFMS-UHFFFAOYSA-N C1C2=CC=CC=C2C2=C1C([Zr]C=1C=CC=C3C4=CC=CC=C4CC=13)=CC=C2 Chemical compound C1C2=CC=CC=C2C2=C1C([Zr]C=1C=CC=C3C4=CC=CC=C4CC=13)=CC=C2 OGFJLWUKRCOFMS-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- LUKADOYBIWUGAR-UHFFFAOYSA-N ClC.C1=CC2=CC=CC=C2C1[Zr](=C(C)C)C1C2=CC=CC=C2C=C1 Chemical compound ClC.C1=CC2=CC=CC=C2C1[Zr](=C(C)C)C1C2=CC=CC=C2C=C1 LUKADOYBIWUGAR-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 208000037062 Polyps Diseases 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 241000746181 Therates Species 0.000 description 1
- QSZGOMRHQRFORD-UHFFFAOYSA-L [Cl-].[Cl-].C=C.C1=CC2=CC=CC=C2C1[Zr+2]C1C2=CC=CC=C2C=C1 Chemical compound [Cl-].[Cl-].C=C.C1=CC2=CC=CC=C2C1[Zr+2]C1C2=CC=CC=C2C=C1 QSZGOMRHQRFORD-UHFFFAOYSA-L 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 150000001925 cycloalkenes Chemical class 0.000 description 1
- IDASTKMEQGPVRR-UHFFFAOYSA-N cyclopenta-1,3-diene;zirconium(2+) Chemical class [Zr+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 IDASTKMEQGPVRR-UHFFFAOYSA-N 0.000 description 1
- SMBQBQBNOXIFSF-UHFFFAOYSA-N dilithium Chemical class [Li][Li] SMBQBQBNOXIFSF-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000012685 gas phase polymerization Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- GEAWFZNTIFJMHR-UHFFFAOYSA-N hepta-1,6-diene Chemical compound C=CCCCC=C GEAWFZNTIFJMHR-UHFFFAOYSA-N 0.000 description 1
- 239000002815 homogeneous catalyst Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- VMRZYTKLQVKYKQ-UHFFFAOYSA-N lithium;1,9-dihydrofluoren-1-ide Chemical compound [Li+].C1=C[C-]=C2CC3=CC=CC=C3C2=C1 VMRZYTKLQVKYKQ-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 150000004291 polyenes Chemical class 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- HKVFGFGPRISDFM-UHFFFAOYSA-N tris(2,3,3-trimethylbutyl)alumane Chemical compound CC(C)(C)C(C)C[Al](CC(C)C(C)(C)C)CC(C)C(C)(C)C HKVFGFGPRISDFM-UHFFFAOYSA-N 0.000 description 1
- VGONMIOMLRCRSS-UHFFFAOYSA-N tris(2,3-dimethylhexyl)alumane Chemical compound CCCC(C)C(C)C[Al](CC(C)C(C)CCC)CC(C)C(C)CCC VGONMIOMLRCRSS-UHFFFAOYSA-N 0.000 description 1
- BENYMJNPVWYYES-UHFFFAOYSA-N tris(2,3-dimethylpentyl)alumane Chemical compound CCC(C)C(C)C[Al](CC(C)C(C)CC)CC(C)C(C)CC BENYMJNPVWYYES-UHFFFAOYSA-N 0.000 description 1
- XZIKSWMNFLIAQP-UHFFFAOYSA-N tris(2,4,4-trimethylpentyl)alumane Chemical compound CC(C)(C)CC(C)C[Al](CC(C)CC(C)(C)C)CC(C)CC(C)(C)C XZIKSWMNFLIAQP-UHFFFAOYSA-N 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- VPGLGRNSAYHXPY-UHFFFAOYSA-L zirconium(2+);dichloride Chemical compound Cl[Zr]Cl VPGLGRNSAYHXPY-UHFFFAOYSA-L 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07F17/00—Metallocenes
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- C—CHEMISTRY; METALLURGY
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- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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Abstract
Description
Claims (1)
- 【特許請求の範囲】 1. (1)式(Y-Cp)(ZR1 m)n(A-Y)rのリガンドを、少なくとも(1+r+p)モル当 量の式LjB又はLMgL'の化合物[式中、Cp、A、Z、R1、m、n、p、r、L及びL'は下 記の意味を有し;基Yは互いに同一か異なって、適切な離脱基であり;Bはアルカ リ又はアルカリ土類金属であり;jは1又は2であり;Bがアルカリ金属である際 はjは1に等しく、Bがアルカリ土類金属である際はjは2に等しい]と反応させ 、及び (2)工程(1)から得られた生成物を少なくとも1モル当量の式ML's化合物[式中 、M及びL'は上記の意味を有し;sは金属の酸化状態に相当する整数で、3〜6の 範囲である]と反応させる 工程からなることを特徴とする、式(I): (Cp)(ZR1 m)n(A)rMLpL'q (I) [式中、(ZR1 m)nはCpとAを結合する二価の基であり、ZはC、Si、Ge、N又はPで あり、R1基は、互いに同一か異なって、水素又は線状もしくは分枝状で飽和もし くは不飽相のC1-C20アルキル、C3-C20シクロアルキル、C6-C20アリール、C7-C20 アルキルアリール又はC7-C20アリールアルキル基であり; Cpは、1以上の置換又は非置換の、飽和、不飽和もしくは芳香族環に任意に縮合 される置換又は非置換のシクロペンタジエニル基(4〜6の炭素原子を含み、任 意に1以上のヘテロ原子を含む)であり; Aは-O-、-S-、-N(R2)-[R2は水素、線状又は分枝状で、飽和もしくは不飽和のC1- C20アルキル、C3-C20シクロアルキル、C6-C20アリール、C7-C20アルキルアリー ル又はC7-C20アリールアルキル]であるか、Cpと同じ意味を有し; Mは元素の周期律表(IUPAC版)の3、4、5、6群又はランタニドもしくはアクチ ニド群に属する遷移金属であり; 置換基Lは、互いに同一か異なって、任意に1以上のSi又はGe原子を含む線状又 は分枝状で、飽和もしくは不飽和のC1-C20アルキル、C3-C20シクロアルキル、C6 -C20アリール、C7-C20アルキルアリール及びC7-C20アリールアルキル基からなる 群から選択されるモノアニオンシグマリガンドであり; 置換基L'は、互いに同一か異なって、ハロゲン又は-OR5[R5はR1と同一の意味を 有する]であり; mは1又は2であり; nは0〜4の範囲であり; rは0又は1であり; rが0である際にnは0であり; pは1〜3の範囲であり;qは0〜2の範囲で、p+qはrが1である際にマイナス 2、rが0である際にマイナス1の金属Mの酸化状態に等しく、p+qは4未満であ る] のシクロペンタジエニルメタロセン化合物の製造方法。 2. (ZR1 m)nが、CR1 2、(CR1 2)2、(CR1 2)3、SiR1 2、GeR1 2、NR1及びPR1(R1は、 請求項1に記載の意味を有する)からなる群から選択される請求項1に記載の方 法。 3. Cpが、シクロペンタジエニル;モノ、ジ、ドリ及びテトラ-メチルシクロ ペンタジエニル;4-tブチル-シクロペンタジエニル;4-アダマンチル-シクロペ ンタジエニル;インデニル;モノ、ジ、トリ及びテトラメチルインデニル;4,5, 6,7-テトラヒドロインデニル;フルオレニル;5,10-ジヒドロインデノ[1,2-b]イ ンドール-10-イル;N-メチル又はN-フェニル-5,10-ジヒドロインデノ[1,2-b]イ ンドール-10-イル;5,6-ジヒドロインデノ[2,1-b]インドール-6-イル;N-メチル 又はN-フェニル-5,6-ジヒドロインデノ[2,1-b]インドール-6-イ10ル;アザペン タレン-4-イル;チアペンタレン-4-イアザペンタレン-6-イル;チアペンタレン- 6-イル;モノ、ジ及びトリメチルアザペンタレン-4-イルからなる群から選択さ れ、AがCpと同じ意味を有する請求項1に記載の方法。 4. Mが、Ti、Zr又はHfである請求項1に記載の方法。 5. 置換基Lは同じであり、メチル、エチル、n-ブチル、sec-ブチル、フェニ ル、ベンジル及び-CH2Si(CH3)3からなる群から選択される請求項1に記載の方法 。 6. L'が、Cl、Br、-OMe、-OEt、-OPr、-OBu及び-OBzからなる群から選択され る請求項1に記載の方法。 7. ML'sが、TiCl4、ZrCl4、HfCl4、ScCl3、YCl3、NbCl5、Ti(OEt)4、Ti(OPr)4 、Ti(OBz)4、Zr(OEt)4、Zr(OPr)4、Zr(OBz)4、Zr(OEt)3Cl、Hf(OEt)4、Hf(OPr)4 、Hf(OBz)4及びそれらのエーテル錯体からなる群から選択される請求項1に記 載の方法。 8. 化合物LjB又はLMgL'において、Lが、メチル、エチル、n-ブチル、sec-ブ チル、フェニル、ベンジル及び-CH2Si(CH3)3からなる群から選択され、BがLi又 はMgであり、L'がCl又はBrである請求項1に記載の方法。 9. Lがメチルである事実で特徴づけられる請求項8に記載の方法。 10. 少なくとも非プロトン性溶媒中で行なわれることを特徴とする請求項1 に記載の方法。 11. 非プロトン性溶媒が、ベンゼン、トルエン、ペンタン、ヘキサン、ヘプ タン及びシクロヘキサンからなる群から選択される芳香族もしくは脂肪族炭化水 素、又はジエチルエーテル及びテトラヒドロフランからなる群から選択されるエ ーテルである請求項10に記載の方法。 12. 工程(1)において、リガンド(Y-Cp)(ZR1 m)n(A-Y)rが、最初に非プロトン 性溶媒に溶解され、LjB又はLMgL'が、得られた溶液に-100〜+80℃の温度範囲で 5〜45分かけて加えられ、最後にML'Sが加えられることを特徴とする請求項1〜 10に記載の方法。 13. LjB又はLMgL'が、非プロトン性溶媒中に溶液形態で加えられることを特 徴とする請求項12に記載の方法。 14. 工程(1)において、LjB又はLMgL'の添加後に、得られた反応混合物が、- 10〜+80℃の温度で1〜6時間、撹拌下で反応させられることを特徴とする請求 項12に記載の方法。 15. 工程(2)において、ML'sとの反応前に、工程(1)で 得られた混合物が、-100〜+80℃の温度に冷却される請求項12に記載の方法。 16. ML'sが、非プロトン性溶媒中で溶液形態であることを特徴とする請求 項15に記載の方法。 17. 工程(2)において、反応混合物が、-100〜+10℃の温度で6〜36時間、反 応させられることを特徴とする請求項15に記載の方法。
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EP98200077.0 | 1998-01-14 | ||
EP98200077 | 1998-01-14 | ||
PCT/EP1999/000188 WO1999036427A1 (en) | 1998-01-14 | 1999-01-14 | Process for the preparation of metallocene compounds |
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JP2001516367A true JP2001516367A (ja) | 2001-09-25 |
JP2001516367A5 JP2001516367A5 (ja) | 2006-04-13 |
JP4208265B2 JP4208265B2 (ja) | 2009-01-14 |
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US (1) | US6191294B1 (ja) |
EP (1) | EP0979232B1 (ja) |
JP (1) | JP4208265B2 (ja) |
KR (1) | KR20000076111A (ja) |
CN (1) | CN1243763C (ja) |
CA (1) | CA2283880A1 (ja) |
DE (1) | DE69903388T2 (ja) |
WO (1) | WO1999036427A1 (ja) |
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JP2005514423A (ja) * | 2002-01-08 | 2005-05-19 | 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 | ジアルキル−アンサ−メタロセンの製造 |
WO2018003389A1 (ja) * | 2016-06-29 | 2018-01-04 | ポリプラスチックス株式会社 | 触媒の製造方法 |
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EP1131328B1 (en) | 1998-11-18 | 2003-05-07 | Basell Polyolefine GmbH | Methylene bridged metallocenes as olefin-polymerization-catalyst components |
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JP3986441B2 (ja) | 2001-04-10 | 2007-10-03 | バセル ポリオレフィン ジーエムビーエイチ | モノハライドまたはジハライドメタロセン化合物の製造方法 |
US7074864B2 (en) | 2001-06-12 | 2006-07-11 | Basell Polyolefine Gmbh | Process for the polymerization of 1-butene |
JP4418228B2 (ja) | 2001-06-22 | 2010-02-17 | バーゼル・ポリオレフィン・ゲーエムベーハー | メタロセン、オレフィンポリマー製造用の触媒系における使用 |
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JP2005510567A (ja) | 2001-11-30 | 2005-04-21 | バセル ポリオレフィン ジーエムビーエイチ | メタロセン化合物およびプロピレンポリマー製造方法 |
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CN101245084B (zh) * | 2007-02-14 | 2013-02-20 | 中国石油天然气股份有限公司 | 含膦取代乙烯基茂金属催化剂及其制备方法和应用 |
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US20110137060A1 (en) | 2008-08-25 | 2011-06-09 | Basell Polyolefin Gmbh | Preparation of ansa metallocene compounds |
KR101673043B1 (ko) | 2009-06-16 | 2016-11-04 | 셰브론 필립스 케미컬 컴퍼니 엘피 | 메탈로센-ssa 촉매시스템을 이용한 알파 올레핀 올리고머화 및 윤활제 블렌드 제조를 위한 생성된 폴리알파올레핀의 용도 |
WO2011044150A1 (en) * | 2009-10-06 | 2011-04-14 | Chevron Phillips Chemical Company Lp | Oligomerization of olefin waxes using metallocene-based catalyst systems |
KR20140075589A (ko) | 2012-12-11 | 2014-06-19 | 주식회사 엘지화학 | 신규한 리간드 화합물, 이의 제조방법, 전이금속 화합물, 및 이의 제조방법 |
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1999
- 1999-01-14 CA CA002283880A patent/CA2283880A1/en not_active Abandoned
- 1999-01-14 JP JP53674499A patent/JP4208265B2/ja not_active Expired - Lifetime
- 1999-01-14 KR KR1019997008199A patent/KR20000076111A/ko not_active Application Discontinuation
- 1999-01-14 EP EP99902538A patent/EP0979232B1/en not_active Expired - Lifetime
- 1999-01-14 CN CNB99800037XA patent/CN1243763C/zh not_active Expired - Fee Related
- 1999-01-14 WO PCT/EP1999/000188 patent/WO1999036427A1/en not_active Application Discontinuation
- 1999-01-14 DE DE69903388T patent/DE69903388T2/de not_active Expired - Lifetime
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2005514423A (ja) * | 2002-01-08 | 2005-05-19 | 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 | ジアルキル−アンサ−メタロセンの製造 |
WO2018003389A1 (ja) * | 2016-06-29 | 2018-01-04 | ポリプラスチックス株式会社 | 触媒の製造方法 |
KR20190007518A (ko) | 2016-06-29 | 2019-01-22 | 포리프라스틱 가부시키가이샤 | 촉매의 제조방법 |
DE112017003262T5 (de) | 2016-06-29 | 2019-03-14 | Polyplastics Co., Ltd. | Verfahren zur Herstellung eines Katalysators |
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CN1243763C (zh) | 2006-03-01 |
KR20000076111A (ko) | 2000-12-26 |
CA2283880A1 (en) | 1999-07-22 |
EP0979232A1 (en) | 2000-02-16 |
EP0979232B1 (en) | 2002-10-09 |
US6191294B1 (en) | 2001-02-20 |
JP4208265B2 (ja) | 2009-01-14 |
DE69903388D1 (de) | 2002-11-14 |
CN1255925A (zh) | 2000-06-07 |
DE69903388T2 (de) | 2003-06-18 |
WO1999036427A1 (en) | 1999-07-22 |
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