JP2016527182A - ルイス塩基配位子を含む金属錯体 - Google Patents
ルイス塩基配位子を含む金属錯体 Download PDFInfo
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- JP2016527182A JP2016527182A JP2016512365A JP2016512365A JP2016527182A JP 2016527182 A JP2016527182 A JP 2016527182A JP 2016512365 A JP2016512365 A JP 2016512365A JP 2016512365 A JP2016512365 A JP 2016512365A JP 2016527182 A JP2016527182 A JP 2016527182A
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- Prior art keywords
- group
- borane
- metal complex
- ligand
- formula
- Prior art date
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- Granted
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- 239000003446 ligand Substances 0.000 title claims abstract description 62
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 25
- 239000002184 metal Substances 0.000 title claims abstract description 25
- 239000002879 Lewis base Substances 0.000 title claims abstract description 12
- 150000007527 lewis bases Chemical class 0.000 title claims abstract description 12
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 claims abstract description 38
- 150000004696 coordination complex Chemical class 0.000 claims abstract description 38
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 27
- 150000001993 dienes Chemical class 0.000 claims abstract description 24
- 229910000085 borane Inorganic materials 0.000 claims abstract description 19
- 101150075118 sub1 gene Proteins 0.000 claims abstract description 15
- 150000001409 amidines Chemical class 0.000 claims abstract description 12
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 12
- 125000001424 substituent group Chemical group 0.000 claims abstract description 12
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 10
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims abstract description 9
- 230000007935 neutral effect Effects 0.000 claims abstract description 8
- 125000000746 allylic group Chemical group 0.000 claims abstract description 3
- -1 allyl borate Chemical group 0.000 claims description 52
- 150000001875 compounds Chemical class 0.000 claims description 31
- 239000003054 catalyst Substances 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 25
- 239000000178 monomer Substances 0.000 claims description 20
- 239000010936 titanium Substances 0.000 claims description 17
- 230000008569 process Effects 0.000 claims description 16
- 125000003118 aryl group Chemical group 0.000 claims description 14
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 13
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims description 11
- 239000002516 radical scavenger Substances 0.000 claims description 10
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 9
- INYHZQLKOKTDAI-UHFFFAOYSA-N 5-ethenylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=C)CC1C=C2 INYHZQLKOKTDAI-UHFFFAOYSA-N 0.000 claims description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 8
- 239000005977 Ethylene Substances 0.000 claims description 8
- 239000007983 Tris buffer Substances 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 8
- 239000004711 α-olefin Substances 0.000 claims description 8
- OJOWICOBYCXEKR-APPZFPTMSA-N (1S,4R)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound CC=C1C[C@@H]2C[C@@H]1C=C2 OJOWICOBYCXEKR-APPZFPTMSA-N 0.000 claims description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 7
- 125000004429 atom Chemical group 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 6
- 150000002430 hydrocarbons Chemical group 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
- OBAJXDYVZBHCGT-UHFFFAOYSA-N tris(pentafluorophenyl)borane Chemical compound FC1=C(F)C(F)=C(F)C(F)=C1B(C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F OBAJXDYVZBHCGT-UHFFFAOYSA-N 0.000 claims description 6
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 230000000379 polymerizing effect Effects 0.000 claims description 5
- SDRZFSPCVYEJTP-UHFFFAOYSA-N 1-ethenylcyclohexene Chemical compound C=CC1=CCCCC1 SDRZFSPCVYEJTP-UHFFFAOYSA-N 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 150000002527 isonitriles Chemical group 0.000 claims description 4
- 150000002825 nitriles Chemical group 0.000 claims description 4
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 claims description 4
- WTQBISBWKRKLIJ-UHFFFAOYSA-N 5-methylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C)CC1C=C2 WTQBISBWKRKLIJ-UHFFFAOYSA-N 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 3
- PCGYNXNSBCFBSU-UHFFFAOYSA-N bis(2,3,4,5,6-pentafluorophenyl)-phenylborane Chemical compound FC1=C(F)C(F)=C(F)C(F)=C1B(C=1C(=C(F)C(F)=C(F)C=1F)F)C1=CC=CC=C1 PCGYNXNSBCFBSU-UHFFFAOYSA-N 0.000 claims description 3
- 150000008282 halocarbons Chemical group 0.000 claims description 3
- 150000002466 imines Chemical group 0.000 claims description 3
- 229910000064 phosphane Inorganic materials 0.000 claims description 3
- 150000003568 thioethers Chemical class 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- GZQXROYFQLBBPK-UHFFFAOYSA-N tris(2,3,5,6-tetrafluorophenyl)borane Chemical compound FC1=CC(F)=C(F)C(B(C=2C(=C(F)C=C(F)C=2F)F)C=2C(=C(F)C=C(F)C=2F)F)=C1F GZQXROYFQLBBPK-UHFFFAOYSA-N 0.000 claims description 3
- LKNHGIFPRLUGEG-UHFFFAOYSA-N tris(3,4,5-trifluorophenyl)borane Chemical compound FC1=C(F)C(F)=CC(B(C=2C=C(F)C(F)=C(F)C=2)C=2C=C(F)C(F)=C(F)C=2)=C1 LKNHGIFPRLUGEG-UHFFFAOYSA-N 0.000 claims description 3
- 239000005922 Phosphane Substances 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 229910052752 metalloid Inorganic materials 0.000 claims description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphane group Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 2
- NPHLURKGGOFSPO-UHFFFAOYSA-N tris(2,3,4,5-tetrafluorophenyl)borane Chemical compound FC1=C(F)C(F)=CC(B(C=2C(=C(F)C(F)=C(F)C=2)F)C=2C(=C(F)C(F)=C(F)C=2)F)=C1F NPHLURKGGOFSPO-UHFFFAOYSA-N 0.000 claims description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 30
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 22
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 22
- 239000000243 solution Substances 0.000 description 21
- 239000002904 solvent Substances 0.000 description 19
- LWNGJAHMBMVCJR-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenoxy)boronic acid Chemical compound OB(O)OC1=C(F)C(F)=C(F)C(F)=C1F LWNGJAHMBMVCJR-UHFFFAOYSA-N 0.000 description 18
- 150000001639 boron compounds Chemical class 0.000 description 16
- 150000001408 amides Chemical class 0.000 description 14
- 125000004432 carbon atom Chemical group C* 0.000 description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 11
- 238000005481 NMR spectroscopy Methods 0.000 description 11
- 125000000217 alkyl group Chemical group 0.000 description 9
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 238000003786 synthesis reaction Methods 0.000 description 8
- 239000012190 activator Substances 0.000 description 7
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 125000002524 organometallic group Chemical group 0.000 description 7
- SDJHPPZKZZWAKF-UHFFFAOYSA-N 2,3-dimethylbuta-1,3-diene Chemical compound CC(=C)C(C)=C SDJHPPZKZZWAKF-UHFFFAOYSA-N 0.000 description 6
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 6
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- 230000004913 activation Effects 0.000 description 6
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 6
- 229910052796 boron Inorganic materials 0.000 description 6
- 239000013078 crystal Substances 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 125000004122 cyclic group Chemical group 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 5
- 150000004291 polyenes Chemical class 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- FAGLEPBREOXSAC-UHFFFAOYSA-N tert-butyl isocyanide Chemical compound CC(C)(C)[N+]#[C-] FAGLEPBREOXSAC-UHFFFAOYSA-N 0.000 description 5
- UXQAEOWCSOPBLF-UHFFFAOYSA-N 2,2,3,3-tetramethyloctane Chemical compound CCCCCC(C)(C)C(C)(C)C UXQAEOWCSOPBLF-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000012298 atmosphere Substances 0.000 description 4
- 229910052731 fluorine Inorganic materials 0.000 description 4
- 125000003800 germyl group Chemical group [H][Ge]([H])([H])[*] 0.000 description 4
- APPOKADJQUIAHP-UHFFFAOYSA-N hexa-2,4-diene Chemical compound CC=CC=CC APPOKADJQUIAHP-UHFFFAOYSA-N 0.000 description 4
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 4
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 4
- WCFQIFDACWBNJT-UHFFFAOYSA-N $l^{1}-alumanyloxy(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]O[Al] WCFQIFDACWBNJT-UHFFFAOYSA-N 0.000 description 3
- PBKONEOXTCPAFI-UHFFFAOYSA-N 1,2,4-trichlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1 PBKONEOXTCPAFI-UHFFFAOYSA-N 0.000 description 3
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 3
- 238000004009 13C{1H}-NMR spectroscopy Methods 0.000 description 3
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 3
- LGLDSEPDYUTBNZ-UHFFFAOYSA-N 3-phenylbuta-1,3-dien-2-ylbenzene Chemical compound C=1C=CC=CC=1C(=C)C(=C)C1=CC=CC=C1 LGLDSEPDYUTBNZ-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000007848 Bronsted acid Substances 0.000 description 3
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 3
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- HFKJQIJFRMRSKM-UHFFFAOYSA-N [3,5-bis(trifluoromethyl)phenoxy]boronic acid Chemical compound OB(O)OC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 HFKJQIJFRMRSKM-UHFFFAOYSA-N 0.000 description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 125000004104 aryloxy group Chemical group 0.000 description 3
- 150000001767 cationic compounds Chemical class 0.000 description 3
- 229940125782 compound 2 Drugs 0.000 description 3
- 229940126214 compound 3 Drugs 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 150000003983 crown ethers Chemical class 0.000 description 3
- JLTDJTHDQAWBAV-UHFFFAOYSA-O dimethyl(phenyl)azanium Chemical compound C[NH+](C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-O 0.000 description 3
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 150000002892 organic cations Chemical class 0.000 description 3
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 3
- 229920000573 polyethylene Polymers 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
- 238000001542 size-exclusion chromatography Methods 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- JFLKFZNIIQFQBS-FNCQTZNRSA-N trans,trans-1,4-Diphenyl-1,3-butadiene Chemical compound C=1C=CC=CC=1\C=C\C=C\C1=CC=CC=C1 JFLKFZNIIQFQBS-FNCQTZNRSA-N 0.000 description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- RJUCIROUEDJQIB-GQCTYLIASA-N (6e)-octa-1,6-diene Chemical compound C\C=C\CCCC=C RJUCIROUEDJQIB-GQCTYLIASA-N 0.000 description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- XWJBRBSPAODJER-UHFFFAOYSA-N 1,7-octadiene Chemical compound C=CCCCCC=C XWJBRBSPAODJER-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
- VQOXUMQBYILCKR-UHFFFAOYSA-N 1-Tridecene Chemical compound CCCCCCCCCCCC=C VQOXUMQBYILCKR-UHFFFAOYSA-N 0.000 description 2
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- ADOBXTDBFNCOBN-UHFFFAOYSA-N 1-heptadecene Chemical compound CCCCCCCCCCCCCCCC=C ADOBXTDBFNCOBN-UHFFFAOYSA-N 0.000 description 2
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
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- PJLHTVIBELQURV-UHFFFAOYSA-N 1-pentadecene Chemical compound CCCCCCCCCCCCCC=C PJLHTVIBELQURV-UHFFFAOYSA-N 0.000 description 2
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
- DCTOHCCUXLBQMS-UHFFFAOYSA-N 1-undecene Chemical compound CCCCCCCCCC=C DCTOHCCUXLBQMS-UHFFFAOYSA-N 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
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- GSNUFIFRDBKVIE-UHFFFAOYSA-N 2,5-dimethylfuran Chemical compound CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 description 2
- KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-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
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 229940126062 Compound A Drugs 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
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- RFUDQCRVCDXBGK-UHFFFAOYSA-L dichloro(propyl)alumane Chemical compound [Cl-].[Cl-].CCC[Al+2] RFUDQCRVCDXBGK-UHFFFAOYSA-L 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-O dicyclohexylazanium Chemical compound C1CCCCC1[NH2+]C1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-O 0.000 description 1
- GGSUCNLOZRCGPQ-UHFFFAOYSA-O diethyl(phenyl)azanium Chemical compound CC[NH+](CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-O 0.000 description 1
- HJXBDPDUCXORKZ-UHFFFAOYSA-N diethylalumane Chemical compound CC[AlH]CC HJXBDPDUCXORKZ-UHFFFAOYSA-N 0.000 description 1
- YNLAOSYQHBDIKW-UHFFFAOYSA-M diethylaluminium chloride Chemical compound CC[Al](Cl)CC YNLAOSYQHBDIKW-UHFFFAOYSA-M 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 125000004212 difluorophenyl group Chemical group 0.000 description 1
- CPDVHGLWIFENDJ-UHFFFAOYSA-N dihexylalumane Chemical compound C(CCCCC)[AlH]CCCCCC CPDVHGLWIFENDJ-UHFFFAOYSA-N 0.000 description 1
- TUTOKIOKAWTABR-UHFFFAOYSA-N dimethylalumane Chemical compound C[AlH]C TUTOKIOKAWTABR-UHFFFAOYSA-N 0.000 description 1
- JGHYBJVUQGTEEB-UHFFFAOYSA-M dimethylalumanylium;chloride Chemical compound C[Al](C)Cl JGHYBJVUQGTEEB-UHFFFAOYSA-M 0.000 description 1
- QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 description 1
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
- XOCWTYIVWYOSGQ-UHFFFAOYSA-N dipropylalumane Chemical compound C(CC)[AlH]CCC XOCWTYIVWYOSGQ-UHFFFAOYSA-N 0.000 description 1
- ZMXPNWBFRPIZFV-UHFFFAOYSA-M dipropylalumanylium;chloride Chemical compound [Cl-].CCC[Al+]CCC ZMXPNWBFRPIZFV-UHFFFAOYSA-M 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- FPULFENIJDPZBX-UHFFFAOYSA-N ethyl 2-isocyanoacetate Chemical compound CCOC(=O)C[N+]#[C-] FPULFENIJDPZBX-UHFFFAOYSA-N 0.000 description 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
- 125000001207 fluorophenyl group Chemical group 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 230000008570 general process Effects 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 1
- GEAWFZNTIFJMHR-UHFFFAOYSA-N hepta-1,6-diene Chemical compound C=CCCCC=C GEAWFZNTIFJMHR-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 125000003936 heterocyclopentadienyl group Chemical group 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- VMLUVDHAXSZZSR-UHFFFAOYSA-L hexylaluminum(2+);dichloride Chemical compound CCCCCC[Al](Cl)Cl VMLUVDHAXSZZSR-UHFFFAOYSA-L 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910001411 inorganic cation Inorganic materials 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 150000004658 ketimines Chemical class 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- IHLVCKWPAMTVTG-UHFFFAOYSA-N lithium;carbanide Chemical compound [Li+].[CH3-] IHLVCKWPAMTVTG-UHFFFAOYSA-N 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- YSTQWZZQKCCBAY-UHFFFAOYSA-L methylaluminum(2+);dichloride Chemical compound C[Al](Cl)Cl YSTQWZZQKCCBAY-UHFFFAOYSA-L 0.000 description 1
- LUJYQXSLRPMWPJ-UHFFFAOYSA-N n,n,2,2-tetramethylpropanimidamide Chemical compound CN(C)C(=N)C(C)(C)C LUJYQXSLRPMWPJ-UHFFFAOYSA-N 0.000 description 1
- ZOYAFVGHWWJVAT-UHFFFAOYSA-N n,n-di(propan-2-yl)ethanimidamide Chemical compound CC(C)N(C(C)C)C(C)=N ZOYAFVGHWWJVAT-UHFFFAOYSA-N 0.000 description 1
- OTCZVWNTUVWFSL-UHFFFAOYSA-N n,n-dicyclohexylethanimidamide Chemical compound C1CCCCC1N(C(=N)C)C1CCCCC1 OTCZVWNTUVWFSL-UHFFFAOYSA-N 0.000 description 1
- VEHZLOXNVVKFAG-UHFFFAOYSA-N n,n-dimethyl-2-phenylethanimidamide Chemical compound CN(C)C(=N)CC1=CC=CC=C1 VEHZLOXNVVKFAG-UHFFFAOYSA-N 0.000 description 1
- CFRKRFIWGWQEOJ-UHFFFAOYSA-N n,n-dimethylcyclohexanecarboximidamide Chemical compound CN(C)C(=N)C1CCCCC1 CFRKRFIWGWQEOJ-UHFFFAOYSA-N 0.000 description 1
- PAXRVGDTBDATMF-UHFFFAOYSA-N n,n-dimethylethanimidamide Chemical compound CN(C)C(C)=N PAXRVGDTBDATMF-UHFFFAOYSA-N 0.000 description 1
- LMZJCMUESMQKNG-UHFFFAOYSA-N n,n-dimethylnaphthalene-1-carboximidamide Chemical compound C1=CC=C2C(C(=N)N(C)C)=CC=CC2=C1 LMZJCMUESMQKNG-UHFFFAOYSA-N 0.000 description 1
- OOHAUGDGCWURIT-UHFFFAOYSA-N n,n-dipentylpentan-1-amine Chemical compound CCCCCN(CCCCC)CCCCC OOHAUGDGCWURIT-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 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 description 1
- JACMPVXHEARCBO-UHFFFAOYSA-N n-pentylpentan-1-amine Chemical compound CCCCCNCCCCC JACMPVXHEARCBO-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- CATWEXRJGNBIJD-UHFFFAOYSA-N n-tert-butyl-2-methylpropan-2-amine Chemical compound CC(C)(C)NC(C)(C)C CATWEXRJGNBIJD-UHFFFAOYSA-N 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 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 description 1
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- NOUWNNABOUGTDQ-UHFFFAOYSA-N octane Chemical compound CCCCCCC[CH2+] NOUWNNABOUGTDQ-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000002097 pentamethylcyclopentadienyl group Chemical group 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 229940100684 pentylamine Drugs 0.000 description 1
- DLRJIFUOBPOJNS-UHFFFAOYSA-N phenetole Chemical compound CCOC1=CC=CC=C1 DLRJIFUOBPOJNS-UHFFFAOYSA-N 0.000 description 1
- 125000004351 phenylcyclohexyl group Chemical group C1(=CC=CC=C1)C1(CCCCC1)* 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 150000003002 phosphanes Chemical group 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229940054334 silver cation Drugs 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- SLRCCWJSBJZJBV-AJNGGQMLSA-N sparteine Chemical compound C1N2CCCC[C@H]2[C@@H]2CN3CCCC[C@H]3[C@H]1C2 SLRCCWJSBJZJBV-AJNGGQMLSA-N 0.000 description 1
- 229960001945 sparteine Drugs 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 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
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- XMRSTLBCBDIKFI-UHFFFAOYSA-N tetradeca-1,13-diene Chemical compound C=CCCCCCCCCCCC=C XMRSTLBCBDIKFI-UHFFFAOYSA-N 0.000 description 1
- RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical compound C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 238000000427 thin-film deposition Methods 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 150000004992 toluidines Chemical class 0.000 description 1
- CFOAUYCPAUGDFF-UHFFFAOYSA-N tosmic Chemical compound CC1=CC=C(S(=O)(=O)C[N+]#[C-])C=C1 CFOAUYCPAUGDFF-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
- ORYGRKHDLWYTKX-UHFFFAOYSA-N trihexylalumane Chemical compound CCCCCC[Al](CCCCCC)CCCCCC ORYGRKHDLWYTKX-UHFFFAOYSA-N 0.000 description 1
- KTDRTOYQXRJJTE-FIFLTTCUSA-N trimethyl-[(1e,3e)-4-trimethylsilylbuta-1,3-dienyl]silane Chemical compound C[Si](C)(C)\C=C\C=C\[Si](C)(C)C KTDRTOYQXRJJTE-FIFLTTCUSA-N 0.000 description 1
- LZTRCELOJRDYMQ-UHFFFAOYSA-N triphenylmethanol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)C1=CC=CC=C1 LZTRCELOJRDYMQ-UHFFFAOYSA-N 0.000 description 1
- CNWZYDSEVLFSMS-UHFFFAOYSA-N tripropylalumane Chemical compound CCC[Al](CCC)CCC CNWZYDSEVLFSMS-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- GIIXTFIYICRGMZ-UHFFFAOYSA-N tris(2,3-dimethylphenyl)phosphane Chemical compound CC1=CC=CC(P(C=2C(=C(C)C=CC=2)C)C=2C(=C(C)C=CC=2)C)=C1C GIIXTFIYICRGMZ-UHFFFAOYSA-N 0.000 description 1
- ABDKAPXRBAPSQN-UHFFFAOYSA-N veratrole Chemical compound COC1=CC=CC=C1OC ABDKAPXRBAPSQN-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000000196 viscometry Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
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- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
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- C07F17/00—Metallocenes
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- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
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Abstract
Description
CyAMX(L)n (1)
式中、
Cyは、シクロペンタジエニルタイプの配位子であり、
Mは、第4族の金属であり;
Aは、式2:
で表される、アミジン含有配位子残基であり;
Xは、共役ジエン配位子、D、およびボラン、Bから誘導される、アリルボレート配位子であり、
Lは、中性のルイス塩基配位子であり、ここで前記金属配位子の数「n」は、1から、18電子則を満足させる量までの範囲である。
好ましい実施態様においては、第4族の金属Mは、チタン(Ti)、ジルコニウム(Zr)、またはハフニウム(Hf)、最も好ましくはチタンである。
好ましいシクロペンタジエニルタイプの配位子は、モノもしくはポリ置換されており、ここでその置換基は、ハロゲン、置換もしくは非置換のヒドロカルビル、置換もしくは非置換のヒドロカルビルオキシ、置換もしくは非置換のシリル、および置換もしくは非置換のゲルミル(germyl)残基、並びにアミドおよびホスフィド基からなる群より選択される。可能な置換基は、ハロゲン、アミド、ホスフィド、アルコキシ、またはアリールオキシ残基である。本明細書で使用するとき、「置換されたシクロペンタジエニルタイプの配位子」という用語は、それが慣用されている意味合いを広くカバーしており、すなわち、π型の結合を介して金属に結合され、通常は金属に対してη5−配位を取っている、5員の炭素環を有する置換された配位子を意味している。
本発明の好ましい実施態様は、式(2)のアミジン含有配位子Aを含む、式(1)の金属錯体に関し、式(2)中、Sub1はアリール残基である。そのような好ましいアミジネート含有配位子の典型的な例は、Sub1が、フェニルまたは置換されたフェニル残基、好ましくはナフチル、2,6−ジメチルフェニル、2,6−ジクロロフェニル、または2,6−ジフルオロフェニルである、式2で表される。
Lがエーテル、チオエーテル、アミン、三級ホスファン、イミン、ニトリル、イソニトリル、または二配位(バイデンテート)または複数配位(オリゴデンテート)供与体である式(1)の金属錯体が好ましい。
好ましい配位子Xは、アリルボレート配位子である。
Mが、Tiを意味し、
Cyが、ペンタメチルシクロペンタジエニルを意味し、
Aが、式(2)のアミジン基を意味し、ここで、
Sub1が、非置換もしくは置換フェニルを意味するが、ここで置換基は、ハロゲン、特にClまたはF、およびC1〜C4−アルキル、特にメチルが好ましく、
Sub2が、−NR4R5を意味するが、ここでR4およびR5は、先に挙げた意味合いを有しており、
Xが、非置換もしくは置換1,3−ブタジエン、特に1,4−ジフェニル−1,3−ブタジエン、2,3−ジフェニル−1,3−ブタジエン、2,3−ジメチル−1,3−ブタジエン、もしくは1,4−ジメチル−1,3−ブタジエン、及び式BQ1Q2Q3のボレート(ここでQ1〜Q3は、先に挙げた意味合いを有する)、好ましくはトリス(ペンタフルオロ−フェニル)ボラン(B(C6F5)3)、から誘導されるアリルボレートを意味し、
Lが、tert−ブチルイソニトリルを意味し、nが1を意味している。
本発明はさらに、本発明による金属錯体を製造するためのプロセスにも関し、そこでは、式(3):
CyAMX (3)
の金属錯体を、ルイス塩基Lと反応させるが、ここで基Cy、A、M、X、およびLは、先に挙げた意味合いを有する。
CyAMD (4)
[式中、Cy、A、およびMは、請求項8におけるのと同じ意味合いを有し、Dは、共役ジエン、好ましくは先に挙げたものを意味する。]
の金属錯体とボランの反応によって得られるのが好ましい。
a)本発明による式(1)の金属錯体
および
b)捕捉剤(スカベンジャー)。
(C1)一般式BQ1Q2Q3で表されるホウ素化合物
(C2)一般式G(BQ1Q2Q3Q4)で表されるホウ素化合物
(C3)一般式(J−H)(BQ1Q2Q3Q4)で表されるホウ素化合物。
(ここで、Bは、三価の原子価状態にあるホウ素原子であり、Q1〜Q3は、既に先に述べたのと同じ意味合いを有し、Q4は、基Q1〜Q3の一つと同じ意味合いを有し、Q1〜Q4は、同一であっても、異なっていてもよい。Gは、無機もしくは有機のカチオンであり、Jは中性のルイス塩基であり、(J−H)は、ブレンステッド酸である。
(E1)一般式T1 aAlZ3−aで表されるオルガノアルミニウム化合物
(E2)一般式{−Al(T2)−O−}bで表される構造を有する環状アルミノキサン
(E3)一般式T3{−Al(T3)−O−}cAlT3 2で表される構造を有する直鎖状アルミノキサン
(ここで、T1、T2、およびT3のそれぞれは、炭化水素基であり、すべてのT1、すべてのT2、およびすべてのT3がそれぞれ、同一であっても、異なっていてもよい。Zは、水素原子またはハロゲン原子を表し、すべてのZが、同一であっても、異なっていてもよい。「a」は、0<a≦3を満足する数を表し、「b」は2以上の整数であり、「c」は、1以上の整数である。)
本発明はさらに、少なくとも1種のオレフィン性モノマーを重合させることによって、ポリマーを重合させるためのプロセスも提供するが、それには前記モノマーを式(1)の金属錯体と接触させることが含まれる。
屈折率(RI)および粘度差測定法(DV=Differential Viscometry)検出器と組み合わせた、サイズ排除クロマトグラフィー(SEC)(SEC−DV)
装置:
PL220(Polymer Laboratories)SEC:PL220 DRI濃度検出器およびViscotek 220R粘度検出器つき。
検出器は、並列配置で操作。
デガッサー:PL−DG 802
データ処理:
Viscotekデータ処理ソフトウェア、TriSEC 2.7以上のバージョン
カラム:
PLgel Olexis(4×)
較正:
標準線状ポリエチレン(PE)(分子量:0.4〜4000kg/mol)を用いた、一般的較正法
温度:
160℃
流量:
1.0mL/min
注入体積:
0.300mL
溶媒/溶出液:
蒸留1,2,4−トリクロロベンゼン(約1g/LのIonol安定剤入り)
サンプル調製:
約150℃、4時間かけて溶解
1.2ミクロンのAgフィルターを通して濾過
サンプル濃度:約1.0mg/mL
固有粘度(IV)は、溶媒としてデカヒドロナフタレンを使用し、135℃で測定した。
一般
すべての操作は、アルゴンまたは窒素(N2)の雰囲気下で、標準的なSchlenkラインまたはドライボックス法を使用して、溶媒は、窒素を吹き込むことにより脱ガスし、適切な乾燥剤のカラムを通過させて乾燥させた。トルエンは、ナトリウム上で還流させ、蒸留した。重水素を含む溶媒は、カリウム上(C6D6)またはP2O5上(CDCl3およびCD2Cl2)で乾燥させ、減圧下で蒸留し、Teflonバルブアンプル中、窒素下で貯蔵した。NMRサンプルは、窒素下に、J.Young Teflonバルブ付きの5mmのWilmad 507−PPチューブの中で調製した。1Hおよび13C−{1H}スペクトルは、Varian Mercury−VX 300スペクトロメーターで、特に断らない限り室温で記録し、残存プロトン溶媒(1H)または溶媒(13C)の共鳴を内部標準とし、テトラメチルシラン(d=0ppm)との比較で報告する。帰属は、二次元の1H−1Hおよび13C−1H NMRの相関実験を用いて確認した。ケミカルシフトはδ(ppm)で、カップリング定数はHzの単位で表した。質量スペクトルは、University of Oxfordの質量スペクトルによって記録した。IRスペクトルは、Nicolet Magna 560 E.S.P.FTIR,Perkin−Elmer 1710、または(空気に対して安定な固体のサンプルについては)Bruker Tensor 27 FT−IR(ダイヤモンドATRモジュール上に薄膜析出)スペクトロメーターを用いて記録した。空気の影響を受けやすいサンプルは、ドライボックスの中でNaCl板の間のヌジョールマルとして調製し、データは、4000〜400cm−1の範囲内で、波数(cm−1)の形で表した。
Cp * Ti{NC(Ph)N i Pr 2 }(η−1,4−C 4 H 4 Me 2 )(化合物A)は、国際公開第2011076772号パンフレットおよび国際公開第2011076775号パンフレットの中の化合物3の記載に従って調製した。
Cp*Ti{NC(Ph)NiPr2}Cl2(3)(1.00g、2.20mmol)のトルエン(15mL)溶液に、撹拌しながら、滴下によりMeLi(2.80mL、Et2O中1.6M、4.40mmol)を添加し、そうして得られた溶液を16時間撹拌した。次に、真空中で揮発分を除去し、次いで黄色の固形物をn−ヘキサン(50mL)に抽出した。その溶液を15mLにまで濃縮し、次いで、−30℃で24時間貯蔵すると、大きな黄色の結晶として所望の反応生成物の結晶化が起き、結晶を単離して、真空中で乾燥させた。収量=0.37g(40%)その生成物は、1H−NMRおよび13C−NMRにより特性解析した。
Cp * Ti{NC(Ph)N i Pr 2 }{η 3 −CH 2 C(Me)C(Me)CH 2 BAr F 3 }の合成(化合物1)
トルエン(20mL)中のCp*Ti{NC(Ph)NiPr2}(η−2,3−C4H4Me2)(0.30g、0.64mmol)の溶液に、トルエン(20mL)中のBArF 3(0.33g、0.64mmol)を添加した。約30秒後に、その溶液がより暗い色に変色した。それをさらに2時間撹拌し、真空中で揮発性成分を除去した。そのようにして得られた緑色の固形分を、ペンタン(3×15mL)を用いて洗浄し、真空中で乾燥させた。収量=0.51g(81%)その生成物は、1H−NMRおよび13C−NMRにより特性解析した。
トルエン(20mL)中のCp*Ti{NC(Ph)NiPr2}(η−1,4−C4H4Me2)(化合物A)(0.30g、0.64mmol)の溶液に、トルエン(20mL)中のBArF 3(0.33g、0.64mmol)を添加した。約30秒後に、その溶液がより暗い緑色に変化した。それをさらに2時間撹拌し、真空中で溶媒を除去した。そうして得られた緑色の固形分を、ペンタン(3×15mL)を用いて洗浄し、真空中で乾燥させた。収量=0.58g(93%)。その生成物は、1H−HNRおよび13C−NMRにより特性解析した。
Cp * Ti{NC(Ph)N i Pr 2 }{η 3 −CH 2 C(Me)C(Me)CH 2 BAr F 3 }( t BuNC)の合成(化合物3)
トルエン(15mL)中のCp*Ti{NC(Ph)NiPr2}{η3−CH2C(Me)C(Me)CH2BArF 3}(化合物1)(0.50g、0.51mmol)の溶液に、t−BuNC(57.7μL、0.51mmol)を添加した。その溶液は直ちに、緑色から暗赤色に変化した。n−ヘキサン(5mL)を添加後、その溶液を16時間静置すると、赤色の固形分の結晶化が起こり、その結晶を単離し、n−ヘキサン(3×10mL)を用いて洗浄し、真空中で乾燥させた。収量=0.39g(72%)。X線回折に好適な単結晶は、室温で、トルエン/n−ヘキサン溶液から成長させた。化合物3は、目立った分解をすることなく、空気中で数日間保存できた。その化合物は、243Kでは、溶液中でジアステレオマーの混合物として存在し、3A対3Bの比率は、60:40であった。
Cp * Ti{NC(Ph)N i Pr 2 }{η 3 −Et(CH) 3 CH 2 BAr F 3 }(tBuNC)の合成(化合物4)
Cp*Ti{NC(Ph)NiPr2}{η3−Et(CH)3CH2BArF 3}(化合物2)(0.50g、0.51mmol)の溶液に、tBuNC(57.7μL、0.51mmol)を添加した。その溶液は直ちに、緑色から暗赤色へと変化し、室温で3時間放置すると、化合物4の暗赤色の結晶が成長していた。それらを単離し、n−ヘキサン(3×10mL)を用いて洗浄し、真空中で乾燥させた。収量=0.42g(77%)化合物4は、目立った分解をすることなく、空気中で数日間保存できた。1H NMR(CD2Cl2,499.9MHz,293K):7.35−6.97(5H,一連のm,C6H5),4.44(1H,dd,EtCHCH,3J=13.9Hz,15.8Hz),3.53(2H,br m,CHMe2),3.08(1H,app d,CH2BArF 3,2J=10.3Hz),2.39(1H,m,CHCH2BArF 3),1.91(1H,app d,CH2BArF 3,2J=10.3Hz),1.78(1H,m,CHEt),1.69(15H,s,C5Me5),1.60(9H,s,tBuNC),1.46(2H,br m,CH 2Me),1.27(6H,br d,CHMe 2),0.97(6H,d,CHMe 2,3J=7.8Hz),0.81(3H,t,CH2 Me,3J=8.2Hz)ppm。13C−{1H} NMR(CD2Cl2,125.8MHz,293K):164.0(NC(Ph)NiPr2),148.8(C6F5),138.9(tBuNC),138.7(C6F5),138.6(i−C6H5),136.9(C6F5),129.6(o−またはm−C6H5),129.1(m−またはo−C6H5),128.8(p−C6H5),125.8(CHCH2BArF 3),124.8(EtCHCH),118.9(C 5Me5),92.2(CHEt),58.9(CMe3),48.1(CHMe2),33.0(CH2BArF 3),31.5(CH2Me),30.5(CMe 3),21.7(CHMe 2),21.3(CHMe 2),19.1(ジエンCH2 Me),12.0(C5 Me 5)ppm(i−C6F5は認められなかった。)。19F NMR(トルエン−d8,282.2MHz,293K):−131.3(m,o−F,6F),−162.8(m,p−F,3F),-166.3(m,m−F,6F)ppm。11B NMR(トルエン−d8,96.2MHz,293K):12.3ppm。IR(NaCl板,ヌジョールマル,cm−1):2177(s,υ(C≡N)),1509(s),1331(s),1269(s),1194(m),1158(m),1136(m),1076(s),1026(w),918(m),885(w),789(w),758(w),726(s),571(m)。分析値(計算値:C52H53BF15N3Ti):C,58.56(58.72);H,5.16(5.02);N,3.73(3.95)%。EI−MS:m/z=512(100%,[B(C6F5)3]+),494(10%,[M−B(C6F5)3−tBu]+),83(80%,[tBuNC]+),57(100%,[NiPr]+)。X線回折に好適な単結晶は、室温で、トルエン/n−ヘキサン溶液から成長させた。
ダブルインターミグ(double intermig)およびバッフルを備えた2リットルのバッチ式オートクレーブ中でバッチ式共重合を実施した。反応温度は、90℃に設定し、Lauda Thermostatにより調節した。フィードストリーム(溶媒およびモノマー)は、各種の吸着媒体と接触させて、当業者には公知の、触媒を失活させる不純物たとえば水、酸素、および極性化合物を除去することにより精製した。重合の際には、エチレンおよびプロピレンモノマーは、その反応器のガスキャップに連続的にフィードした。背圧バルブによって、反応器の圧力を一定に保った。
Claims (15)
- 式(1)の金属錯体。
CyAMX(L)n (1)
[式中、
Cyは、シクロペンタジエニルタイプの配位子であり;
Mは、第4族の金属であり;
Aは、下記式2:
前記アミジン含有配位子は、そのイミン窒素原子を介して金属Mに共有結合的に結合されており、Sub1は第14族原子を含む置換基であって、第14族原子を介してSub1がイミン炭素原子に結合しており、Sub2は第15族のヘテロ原子を含む置換基であって、第15族のヘテロ原子を介してSub2がイミン炭素原子に結合しており;
Xは、共役ジエン配位子、D、およびボラン、Bから誘導される、アリルボレート配位子であり;
Lは、中性のルイス塩基配位子であり、ここで前記金属配位子の数「n」は、1から、18電子則の条件に合う量までの範囲である。] - Lが、エーテル、チオエーテル、アミン、三級ホスファン、イミン、ニトリル、イソニトリル、または二座もしくは多座供与体である、請求項1に記載の金属錯体。
- LがtBuNCである、請求項1〜2のいずれか一項に記載の金属錯体。
- Mがチタンである、請求項1〜3のいずれか一項に記載の金属錯体。
- nが1または2である、請求項1〜4の少なくとも1項に記載の金属錯体。
- Xが、ジエンと一般式BQ1Q2Q3のボランとから誘導されるアリルボレート配位子であって、Q1〜Q3が個々に、ハロゲン原子、炭化水素基、ハロゲン化炭化水素基、置換されたシリル基、アルコキシ基、またはジ置換されたアミノ基であり、それらが同一であっても、異なっていてもよく、特にトリス(ペンタフルオロフェニル)ボラン、トリス(2,3,5,6−テトラフルオロフェニル)ボラン、トリス(2,3,4,5−テトラフルオロフェニル)ボラン、トリス(3,4,5−トリフルオロフェニル)ボラン、トリス(2,3,4−トリフルオロフェニル)ボラン、フェニルビス(ペンタフルオロフェニル)ボラン、またはトリス(ペンタフルオロフェニル)ボラン(B(C6F5)3)である、請求項1〜5の少なくとも1項に記載の金属錯体。
- Sub1が、フェニルまたは置換されたフェニル残基であり、Sub2が、式−NR4R5のアミノ基であり、R4およびR5が、個々に、脂肪族ヒドロカルビル、ハロゲン化脂肪族ヒドロカルビル、芳香族ヒドロカルビル、ハロゲン化芳香族ヒドロカルボニル残基の群から選択され、ここでR4が、場合によっては、R5またはSub1と共にヘテロサイクリック構造を形成している、請求項1〜6の少なくとも1項に記載の金属錯体。
- 請求項1〜7の少なくとも1項に記載の金属錯体を製造するための方法であって、
式(3):
CyAMX (3)
の金属錯体を、ルイス塩基Lと反応させ、基Cy、A、M、X、およびLが、請求項1〜7の少なくとも1項におけるのと同じ意味合いを有する、製造方法。 - 式(3)の金属錯体が、下記式(4)の金属錯体とボランの反応によって得られる、請求項8に記載の、製造方法。
CyAMD (4)
[式中、Cy、A、およびMは、請求項8におけるのと同じ意味合いを有し、Dは、共役ジエンを意味する。] - a)請求項1〜7の少なくとも1項に記載の金属錯体、
および
b)捕捉剤、
を含む触媒系。 - 前記捕捉剤b)が、第1〜13族の金属またはメタロイドのヒドロカルビル、またはそれと、第15族または第16族の原子を含む少なくとも1種の立体障害のある化合物との反応生成物である、請求項10に記載の触媒系。
- 少なくとも1種のオレフィン性モノマーを重合させることによる、ポリマーを製造する方法であって、前記モノマーを、請求項1〜7の少なくとも1項に記載の触媒と接触させることを含む、方法。
- 少なくとも1種のオレフィン性モノマーを重合させることによってポリマーを製造する方法であって、前記モノマーを、請求項10〜11の少なくとも1項に記載の触媒系と接触させることを含む、方法。
- オレフィン性モノマーとして、エチレンと、少なくともC3〜C12−α−オレフィンとが使用される、請求項12に記載の製造方法。
- エチレン、少なくとも1種のC3〜12アルファオレフィン、ならびに、少なくとも1種の非共役ジエン、好ましくは、5−メチレン−2−ノルボルネン、5−エチリデン−2−ノルボルネン、5−ビニルノルボルネン、2,5−ノルボルナジエン、ジシクロペンタジエン、およびビニルシクロヘキセンからなる群より選択される、特に5−エチリデン−2−ノルボルネンおよび5−ビニルノルボルネンからなる群より選択される少なくとも1種の非共役ジエンが、オレフィン性モノマーとして使用される、請求項12または14の少なくとも1項に記載の製造方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP13167138.0A EP2801579B1 (en) | 2013-05-08 | 2013-05-08 | Metal complex with a Lewis base ligand |
EP13167138.0 | 2013-05-08 | ||
PCT/EP2014/059354 WO2014180913A1 (en) | 2013-05-08 | 2014-05-07 | Metal complex with a lewis base ligand |
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JP2021521225A (ja) * | 2018-04-16 | 2021-08-26 | アランセオ・ネザーランズ・ベー・フェー | アミジン及びインドールと縮環したシクロペンタジエニル配位子を含む金属錯体 |
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EP2902420B1 (en) * | 2014-01-29 | 2019-06-12 | Arlanxeo Netherlands B.V. | Metal complex with a cyclic amidine ligand |
EP3272761A1 (en) * | 2016-07-22 | 2018-01-24 | Arlanxeo Netherlands B.V. | Metall complex comprising amidine and substituted cyclopentadienyl ligands |
KR101927184B1 (ko) | 2016-12-09 | 2018-12-10 | 현대자동차 주식회사 | 엔진 시스템의 진단 방법 및 장치 |
EP3638730B1 (en) | 2017-06-14 | 2024-05-01 | ExxonMobil Chemical Patents Inc. | Ethylene copolymer blends for cross-linking applications |
US11132621B2 (en) * | 2017-11-15 | 2021-09-28 | International Business Machines Corporation | Correction of reaction rules databases by active learning |
EP3853265A1 (en) * | 2018-09-18 | 2021-07-28 | Arlanxeo Netherlands B.V. | Catalyst mixture |
WO2022004529A1 (ja) * | 2020-06-29 | 2022-01-06 | ポリプラスチックス株式会社 | 環状オレフィン共重合体の製造方法、及びノルボルネン単量体とエチレンとの共重合用の触媒組成物 |
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EP1426379B1 (en) * | 2001-09-14 | 2009-11-11 | Sumitomo Chemical Company, Limited | Transition metal complex,catalyst for olefin polymerization, and process for producing olefin polymer with the same |
WO2005090418A1 (en) | 2004-03-17 | 2005-09-29 | Dsm Ip Assets B.V. | Polimerization catalyst comprising an amidine ligand |
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JP2021521225A (ja) * | 2018-04-16 | 2021-08-26 | アランセオ・ネザーランズ・ベー・フェー | アミジン及びインドールと縮環したシクロペンタジエニル配位子を含む金属錯体 |
JP7322062B2 (ja) | 2018-04-16 | 2023-08-07 | アランセオ・ネザーランズ・ベー・フェー | アミジン及びインドールと縮環したシクロペンタジエニル配位子を含む金属錯体 |
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CA2909927C (en) | 2021-10-19 |
BR112015027980A8 (pt) | 2017-10-03 |
US20160115265A1 (en) | 2016-04-28 |
KR20160016775A (ko) | 2016-02-15 |
CN105209473A (zh) | 2015-12-30 |
EP2801579B1 (en) | 2016-10-19 |
EP2801579A1 (en) | 2014-11-12 |
WO2014180913A1 (en) | 2014-11-13 |
KR102200242B1 (ko) | 2021-01-11 |
US9546233B2 (en) | 2017-01-17 |
CA2909927A1 (en) | 2014-11-13 |
BR112015027980A2 (pt) | 2017-09-05 |
SA515370102B1 (ar) | 2016-12-18 |
BR112015027980B1 (pt) | 2021-04-13 |
JP6243517B2 (ja) | 2017-12-06 |
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