JP4630078B2 - アリールホウ素化合物の安定化方法および安定化組成物 - Google Patents
アリールホウ素化合物の安定化方法および安定化組成物 Download PDFInfo
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- JP4630078B2 JP4630078B2 JP2005021556A JP2005021556A JP4630078B2 JP 4630078 B2 JP4630078 B2 JP 4630078B2 JP 2005021556 A JP2005021556 A JP 2005021556A JP 2005021556 A JP2005021556 A JP 2005021556A JP 4630078 B2 JP4630078 B2 JP 4630078B2
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- Prior art keywords
- group
- tris
- borane
- pentafluorophenyl
- substituted
- Prior art date
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- -1 aryl boron compounds Chemical class 0.000 title claims description 175
- 238000000034 method Methods 0.000 title claims description 39
- 230000000087 stabilizing effect Effects 0.000 title claims description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 90
- 150000001875 compounds Chemical class 0.000 claims description 75
- 239000002904 solvent Substances 0.000 claims description 75
- 239000004215 Carbon black (E152) Substances 0.000 claims description 49
- 229930195733 hydrocarbon Natural products 0.000 claims description 49
- 150000002430 hydrocarbons Chemical class 0.000 claims description 49
- 239000003381 stabilizer Substances 0.000 claims description 40
- 125000003118 aryl group Chemical group 0.000 claims description 36
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 21
- 125000001424 substituent group Chemical group 0.000 claims description 19
- 125000003545 alkoxy group Chemical group 0.000 claims description 18
- 239000002002 slurry Substances 0.000 claims description 18
- 125000005843 halogen group Chemical group 0.000 claims description 17
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 17
- 230000006641 stabilisation Effects 0.000 claims description 15
- 238000011105 stabilization Methods 0.000 claims description 15
- 125000000623 heterocyclic group Chemical group 0.000 claims description 14
- 229910052760 oxygen Inorganic materials 0.000 claims description 14
- 239000001301 oxygen Substances 0.000 claims description 14
- 229910052731 fluorine Inorganic materials 0.000 claims description 9
- 125000001153 fluoro group Chemical group F* 0.000 claims description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 150000002926 oxygen Chemical class 0.000 claims description 7
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 4
- 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 description 78
- 239000000243 solution Substances 0.000 description 50
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 48
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 40
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 36
- 238000003860 storage Methods 0.000 description 34
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 30
- 239000012085 test solution Substances 0.000 description 29
- 238000004519 manufacturing process Methods 0.000 description 22
- 239000007983 Tris buffer Substances 0.000 description 20
- 229910000085 borane Inorganic materials 0.000 description 20
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 9
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 8
- 238000000806 fluorine-19 nuclear magnetic resonance spectrum Methods 0.000 description 8
- 239000002994 raw material Substances 0.000 description 8
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical group CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 239000012046 mixed solvent Substances 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 238000009835 boiling Methods 0.000 description 6
- 239000006227 byproduct Substances 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 150000002170 ethers Chemical class 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 230000002401 inhibitory effect Effects 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 125000003107 substituted aryl group Chemical group 0.000 description 5
- SPEUIVXLLWOEMJ-UHFFFAOYSA-N 1,1-dimethoxyethane Chemical group COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-N 0.000 description 4
- WACNXHCZHTVBJM-UHFFFAOYSA-N 1,2,3,4,5-pentafluorobenzene Chemical compound FC1=CC(F)=C(F)C(F)=C1F WACNXHCZHTVBJM-UHFFFAOYSA-N 0.000 description 4
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 4
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 4
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 4
- 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 description 4
- 150000001639 boron compounds Chemical class 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 4
- 230000003247 decreasing effect Effects 0.000 description 4
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 4
- 125000001624 naphthyl group Chemical group 0.000 description 4
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 4
- RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 description 4
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 3
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 3
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 230000002194 synthesizing effect Effects 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- 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 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 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical group CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
- FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 description 2
- GWHJZXXIDMPWGX-UHFFFAOYSA-N 1,2,4-trimethylbenzene Chemical compound CC1=CC=C(C)C(C)=C1 GWHJZXXIDMPWGX-UHFFFAOYSA-N 0.000 description 2
- AUHZEENZYGFFBQ-UHFFFAOYSA-N 1,3,5-trimethylbenzene Chemical compound CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 2
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical group C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 2
- XEKTVXADUPBFOA-UHFFFAOYSA-N 1-bromo-2,3,4,5,6-pentafluorobenzene Chemical compound FC1=C(F)C(F)=C(Br)C(F)=C1F XEKTVXADUPBFOA-UHFFFAOYSA-N 0.000 description 2
- KGCDGLXSBHJAHZ-UHFFFAOYSA-N 1-chloro-2,3,4,5,6-pentafluorobenzene Chemical compound FC1=C(F)C(F)=C(Cl)C(F)=C1F KGCDGLXSBHJAHZ-UHFFFAOYSA-N 0.000 description 2
- NQMUGNMMFTYOHK-UHFFFAOYSA-N 1-methoxynaphthalene Chemical compound C1=CC=C2C(OC)=CC=CC2=C1 NQMUGNMMFTYOHK-UHFFFAOYSA-N 0.000 description 2
- ARGCQEVBJHPOGB-UHFFFAOYSA-N 2,5-dihydrofuran Chemical compound C1OCC=C1 ARGCQEVBJHPOGB-UHFFFAOYSA-N 0.000 description 2
- GSNUFIFRDBKVIE-UHFFFAOYSA-N 2,5-dimethylfuran Chemical compound CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 description 2
- OXMIDRBAFOEOQT-UHFFFAOYSA-N 2,5-dimethyloxolane Chemical compound CC1CCC(C)O1 OXMIDRBAFOEOQT-UHFFFAOYSA-N 0.000 description 2
- VQKFNUFAXTZWDK-UHFFFAOYSA-N 2-Methylfuran Chemical compound CC1=CC=CO1 VQKFNUFAXTZWDK-UHFFFAOYSA-N 0.000 description 2
- KJRRQXYWFQKJIP-UHFFFAOYSA-N 3-methylfuran Chemical compound CC=1C=COC=1 KJRRQXYWFQKJIP-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
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- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical group C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- OCKPCBLVNKHBMX-UHFFFAOYSA-N butylbenzene Chemical compound CCCCC1=CC=CC=C1 OCKPCBLVNKHBMX-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000003426 co-catalyst Substances 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- LJSQFQKUNVCTIA-UHFFFAOYSA-N diethyl sulfide Chemical compound CCSCC LJSQFQKUNVCTIA-UHFFFAOYSA-N 0.000 description 2
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 2
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000011968 lewis acid catalyst Substances 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 2
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
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- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- OTCKOJUMXQWKQG-UHFFFAOYSA-L magnesium bromide Chemical compound [Mg+2].[Br-].[Br-] OTCKOJUMXQWKQG-UHFFFAOYSA-L 0.000 description 2
- 229910001623 magnesium bromide Inorganic materials 0.000 description 2
- OVCLXQXUDAEKFN-UHFFFAOYSA-L magnesium;bromide;fluoride Chemical compound [F-].[Mg+2].[Br-] OVCLXQXUDAEKFN-UHFFFAOYSA-L 0.000 description 2
- CFQHVABJRDZBGV-UHFFFAOYSA-L magnesium;chloride;fluoride Chemical compound [F-].[Mg+2].[Cl-] CFQHVABJRDZBGV-UHFFFAOYSA-L 0.000 description 2
- 239000012968 metallocene catalyst Substances 0.000 description 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
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- 229940038384 octadecane Drugs 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
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- 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 2
- YCOZIPAWZNQLMR-UHFFFAOYSA-N pentadecane Chemical compound CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000002685 polymerization catalyst Substances 0.000 description 2
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- 238000007151 ring opening polymerisation reaction Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
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- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 2
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- IIYFAKIEWZDVMP-UHFFFAOYSA-N tridecane Chemical compound CCCCCCCCCCCCC IIYFAKIEWZDVMP-UHFFFAOYSA-N 0.000 description 2
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- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
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- FMHAUDKGLSPVPQ-UHFFFAOYSA-N 1,3-dioxane;1,4-dioxane Chemical compound C1COCOC1.C1COCCO1 FMHAUDKGLSPVPQ-UHFFFAOYSA-N 0.000 description 1
- ABADUMLIAZCWJD-UHFFFAOYSA-N 1,3-dioxole Chemical group C1OC=CO1 ABADUMLIAZCWJD-UHFFFAOYSA-N 0.000 description 1
- KVGZZAHHUNAVKZ-UHFFFAOYSA-N 1,4-Dioxin Chemical group O1C=COC=C1 KVGZZAHHUNAVKZ-UHFFFAOYSA-N 0.000 description 1
- HIZVCIIORGCREW-UHFFFAOYSA-N 1,4-dioxene Chemical group C1COC=CO1 HIZVCIIORGCREW-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- APWZAIZNWQFZBK-UHFFFAOYSA-N 1-ethoxynaphthalene Chemical compound C1=CC=C2C(OCC)=CC=CC2=C1 APWZAIZNWQFZBK-UHFFFAOYSA-N 0.000 description 1
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- BEUPCRVYKDLUGA-UHFFFAOYSA-N tris(2,4,6-trichlorophenyl)borane Chemical compound ClC1=CC(Cl)=CC(Cl)=C1B(C=1C(=CC(Cl)=CC=1Cl)Cl)C1=C(Cl)C=C(Cl)C=C1Cl BEUPCRVYKDLUGA-UHFFFAOYSA-N 0.000 description 1
- DPMRGSOQMBLRBZ-UHFFFAOYSA-N tris(2,4,6-trifluoro-3-methoxyphenyl)borane Chemical compound COC1=C(F)C=C(F)C(B(C=2C(=C(OC)C(F)=CC=2F)F)C=2C(=C(OC)C(F)=CC=2F)F)=C1F DPMRGSOQMBLRBZ-UHFFFAOYSA-N 0.000 description 1
- HPKBFHDRGPIYAG-UHFFFAOYSA-N tris(2,4,6-trifluorophenyl)borane Chemical compound FC1=CC(F)=CC(F)=C1B(C=1C(=CC(F)=CC=1F)F)C1=C(F)C=C(F)C=C1F HPKBFHDRGPIYAG-UHFFFAOYSA-N 0.000 description 1
- KGPQPNPIOBUSBP-UHFFFAOYSA-N tris(2,4-dibromo-5-ethoxyphenyl)borane Chemical compound C1=C(Br)C(OCC)=CC(B(C=2C(=CC(Br)=C(OCC)C=2)Br)C=2C(=CC(Br)=C(OCC)C=2)Br)=C1Br KGPQPNPIOBUSBP-UHFFFAOYSA-N 0.000 description 1
- NCZPFNQVFYQXLZ-UHFFFAOYSA-N tris(2,4-dibromo-5-ethylphenyl)borane Chemical compound C1=C(Br)C(CC)=CC(B(C=2C(=CC(Br)=C(CC)C=2)Br)C=2C(=CC(Br)=C(CC)C=2)Br)=C1Br NCZPFNQVFYQXLZ-UHFFFAOYSA-N 0.000 description 1
- BRGKYGKZVKJDSH-UHFFFAOYSA-N tris(2,4-dibromo-6-ethoxyphenyl)borane Chemical compound CCOC1=CC(Br)=CC(Br)=C1B(C=1C(=CC(Br)=CC=1Br)OCC)C1=C(Br)C=C(Br)C=C1OCC BRGKYGKZVKJDSH-UHFFFAOYSA-N 0.000 description 1
- UMSURODHDQDPDX-UHFFFAOYSA-N tris(2,4-dichloro-5-ethoxyphenyl)borane Chemical compound C1=C(Cl)C(OCC)=CC(B(C=2C(=CC(Cl)=C(OCC)C=2)Cl)C=2C(=CC(Cl)=C(OCC)C=2)Cl)=C1Cl UMSURODHDQDPDX-UHFFFAOYSA-N 0.000 description 1
- IQIHXVQUPXPHOE-UHFFFAOYSA-N tris(2,4-dichloro-5-ethylphenyl)borane Chemical compound C1=C(Cl)C(CC)=CC(B(C=2C(=CC(Cl)=C(CC)C=2)Cl)C=2C(=CC(Cl)=C(CC)C=2)Cl)=C1Cl IQIHXVQUPXPHOE-UHFFFAOYSA-N 0.000 description 1
- SGPMWDSBQCQUNK-UHFFFAOYSA-N tris(2,4-dichloro-5-methoxyphenyl)borane Chemical compound C1=C(Cl)C(OC)=CC(B(C=2C(=CC(Cl)=C(OC)C=2)Cl)C=2C(=CC(Cl)=C(OC)C=2)Cl)=C1Cl SGPMWDSBQCQUNK-UHFFFAOYSA-N 0.000 description 1
- RVGZVWRHDBULMJ-UHFFFAOYSA-N tris(2,4-dichloro-5-methylphenyl)borane Chemical compound C1=C(Cl)C(C)=CC(B(C=2C(=CC(Cl)=C(C)C=2)Cl)C=2C(=CC(Cl)=C(C)C=2)Cl)=C1Cl RVGZVWRHDBULMJ-UHFFFAOYSA-N 0.000 description 1
- WQCGQFHIDDHALF-UHFFFAOYSA-N tris(2,4-dichloro-6-ethoxyphenyl)borane Chemical compound CCOC1=CC(Cl)=CC(Cl)=C1B(C=1C(=CC(Cl)=CC=1Cl)OCC)C1=C(Cl)C=C(Cl)C=C1OCC WQCGQFHIDDHALF-UHFFFAOYSA-N 0.000 description 1
- GDWHEVASALRFLL-UHFFFAOYSA-N tris(2,4-dichloro-6-methoxyphenyl)borane Chemical compound COC1=CC(Cl)=CC(Cl)=C1B(C=1C(=CC(Cl)=CC=1Cl)OC)C1=C(Cl)C=C(Cl)C=C1OC GDWHEVASALRFLL-UHFFFAOYSA-N 0.000 description 1
- MUDVEGNBCFIRDK-UHFFFAOYSA-N tris(2,4-difluoro-5-methylphenyl)borane Chemical compound C1=C(F)C(C)=CC(B(C=2C(=CC(F)=C(C)C=2)F)C=2C(=CC(F)=C(C)C=2)F)=C1F MUDVEGNBCFIRDK-UHFFFAOYSA-N 0.000 description 1
- SIBVKDZXLXFOGI-UHFFFAOYSA-N tris(2,4-difluoro-6-methoxyphenyl)borane Chemical compound COC1=CC(F)=CC(F)=C1B(C=1C(=CC(F)=CC=1F)OC)C1=C(F)C=C(F)C=C1OC SIBVKDZXLXFOGI-UHFFFAOYSA-N 0.000 description 1
- TXGKHZJTFCFSIQ-UHFFFAOYSA-N tris(2,5-dichlorophenyl)borane Chemical compound ClC1=CC=C(Cl)C(B(C=2C(=CC=C(Cl)C=2)Cl)C=2C(=CC=C(Cl)C=2)Cl)=C1 TXGKHZJTFCFSIQ-UHFFFAOYSA-N 0.000 description 1
- ZEYPPUQLVIMERA-UHFFFAOYSA-N tris(2,5-difluorophenyl)borane Chemical compound FC1=CC=C(F)C(B(C=2C(=CC=C(F)C=2)F)C=2C(=CC=C(F)C=2)F)=C1 ZEYPPUQLVIMERA-UHFFFAOYSA-N 0.000 description 1
- IMPUMYDHRQJZLQ-UHFFFAOYSA-N tris(2,6-dibromo-3-ethoxyphenyl)borane Chemical compound CCOC1=CC=C(Br)C(B(C=2C(=C(OCC)C=CC=2Br)Br)C=2C(=C(OCC)C=CC=2Br)Br)=C1Br IMPUMYDHRQJZLQ-UHFFFAOYSA-N 0.000 description 1
- SXWXRBBAHXLDBK-UHFFFAOYSA-N tris(2,6-dibromo-3-ethylphenyl)borane Chemical compound CCC1=CC=C(Br)C(B(C=2C(=C(CC)C=CC=2Br)Br)C=2C(=C(CC)C=CC=2Br)Br)=C1Br SXWXRBBAHXLDBK-UHFFFAOYSA-N 0.000 description 1
- HNYFZYNSDWUHRE-UHFFFAOYSA-N tris(2,6-dibromo-4-ethoxyphenyl)borane Chemical compound BrC1=CC(OCC)=CC(Br)=C1B(C=1C(=CC(OCC)=CC=1Br)Br)C1=C(Br)C=C(OCC)C=C1Br HNYFZYNSDWUHRE-UHFFFAOYSA-N 0.000 description 1
- CEWVFFOXACMBDF-UHFFFAOYSA-N tris(2,6-dichloro-3-ethoxyphenyl)borane Chemical compound CCOC1=CC=C(Cl)C(B(C=2C(=C(OCC)C=CC=2Cl)Cl)C=2C(=C(OCC)C=CC=2Cl)Cl)=C1Cl CEWVFFOXACMBDF-UHFFFAOYSA-N 0.000 description 1
- CUKCCIIHSRRLOQ-UHFFFAOYSA-N tris(2,6-dichloro-3-ethylphenyl)borane Chemical compound CCC1=CC=C(Cl)C(B(C=2C(=C(CC)C=CC=2Cl)Cl)C=2C(=C(CC)C=CC=2Cl)Cl)=C1Cl CUKCCIIHSRRLOQ-UHFFFAOYSA-N 0.000 description 1
- HCNQFTANBYXALY-UHFFFAOYSA-N tris(2,6-dichloro-3-methylphenyl)borane Chemical compound CC1=CC=C(Cl)C(B(C=2C(=C(C)C=CC=2Cl)Cl)C=2C(=C(C)C=CC=2Cl)Cl)=C1Cl HCNQFTANBYXALY-UHFFFAOYSA-N 0.000 description 1
- NXNBZERBXMAQQK-UHFFFAOYSA-N tris(2,6-dichloro-4-ethoxyphenyl)borane Chemical compound ClC1=CC(OCC)=CC(Cl)=C1B(C=1C(=CC(OCC)=CC=1Cl)Cl)C1=C(Cl)C=C(OCC)C=C1Cl NXNBZERBXMAQQK-UHFFFAOYSA-N 0.000 description 1
- YYMNGMNATIUCJU-UHFFFAOYSA-N tris(2,6-dichloro-4-methoxyphenyl)borane Chemical compound ClC1=CC(OC)=CC(Cl)=C1B(C=1C(=CC(OC)=CC=1Cl)Cl)C1=C(Cl)C=C(OC)C=C1Cl YYMNGMNATIUCJU-UHFFFAOYSA-N 0.000 description 1
- XFDAMADSSAELOR-UHFFFAOYSA-N tris(2,6-difluoro-3-methoxyphenyl)borane Chemical compound COC1=CC=C(F)C(B(C=2C(=C(OC)C=CC=2F)F)C=2C(=C(OC)C=CC=2F)F)=C1F XFDAMADSSAELOR-UHFFFAOYSA-N 0.000 description 1
- BJDZTCMHKGMRPE-UHFFFAOYSA-N tris(2,6-difluoro-3-methylphenyl)borane Chemical compound CC1=CC=C(F)C(B(C=2C(=C(C)C=CC=2F)F)C=2C(=C(C)C=CC=2F)F)=C1F BJDZTCMHKGMRPE-UHFFFAOYSA-N 0.000 description 1
- BPKWIPVVSDWONU-UHFFFAOYSA-N tris(2,6-difluoro-4-methoxyphenyl)borane Chemical compound FC1=CC(OC)=CC(F)=C1B(C=1C(=CC(OC)=CC=1F)F)C1=C(F)C=C(OC)C=C1F BPKWIPVVSDWONU-UHFFFAOYSA-N 0.000 description 1
- WIXDUPFRLJCPOW-UHFFFAOYSA-N tris(2-ethyl-3,4,6-trifluorophenyl)borane Chemical compound CCC1=C(F)C(F)=CC(F)=C1B(C=1C(=C(F)C(F)=CC=1F)CC)C1=C(F)C=C(F)C(F)=C1CC WIXDUPFRLJCPOW-UHFFFAOYSA-N 0.000 description 1
- FHZNJCMKNSVABH-UHFFFAOYSA-N tris(2-ethyl-3,5-difluorophenyl)borane Chemical compound CCC1=C(F)C=C(F)C=C1B(C=1C(=C(F)C=C(F)C=1)CC)C1=CC(F)=CC(F)=C1CC FHZNJCMKNSVABH-UHFFFAOYSA-N 0.000 description 1
- YQUAFTAMTKFNFA-UHFFFAOYSA-N tris(3,4,6-tribromo-2-ethylphenyl)borane Chemical compound CCC1=C(Br)C(Br)=CC(Br)=C1B(C=1C(=C(Br)C(Br)=CC=1Br)CC)C1=C(Br)C=C(Br)C(Br)=C1CC YQUAFTAMTKFNFA-UHFFFAOYSA-N 0.000 description 1
- BRGOINCUOIVITF-UHFFFAOYSA-N tris(3,4,6-trichloro-2-ethylphenyl)borane Chemical compound CCC1=C(Cl)C(Cl)=CC(Cl)=C1B(C=1C(=C(Cl)C(Cl)=CC=1Cl)CC)C1=C(Cl)C=C(Cl)C(Cl)=C1CC BRGOINCUOIVITF-UHFFFAOYSA-N 0.000 description 1
- BWQJGGDQFAWMTN-UHFFFAOYSA-N tris(3,4,6-trichloro-2-methylphenyl)borane Chemical compound CC1=C(Cl)C(Cl)=CC(Cl)=C1B(C=1C(=C(Cl)C(Cl)=CC=1Cl)C)C1=C(Cl)C=C(Cl)C(Cl)=C1C BWQJGGDQFAWMTN-UHFFFAOYSA-N 0.000 description 1
- USLQZXAOHCFWGA-UHFFFAOYSA-N tris(3,5-dibromo-2-ethylphenyl)borane Chemical compound CCC1=C(Br)C=C(Br)C=C1B(C=1C(=C(Br)C=C(Br)C=1)CC)C1=CC(Br)=CC(Br)=C1CC USLQZXAOHCFWGA-UHFFFAOYSA-N 0.000 description 1
- RSRYRUDDBXEJIC-UHFFFAOYSA-N tris(3,5-dichloro-2-ethoxyphenyl)borane Chemical compound CCOC1=C(Cl)C=C(Cl)C=C1B(C=1C(=C(Cl)C=C(Cl)C=1)OCC)C1=CC(Cl)=CC(Cl)=C1OCC RSRYRUDDBXEJIC-UHFFFAOYSA-N 0.000 description 1
- RMMGGFLXSVRBMN-UHFFFAOYSA-N tris(3,5-dichloro-2-ethylphenyl)borane Chemical compound CCC1=C(Cl)C=C(Cl)C=C1B(C=1C(=C(Cl)C=C(Cl)C=1)CC)C1=CC(Cl)=CC(Cl)=C1CC RMMGGFLXSVRBMN-UHFFFAOYSA-N 0.000 description 1
- MSAPLRJYZBZUIZ-UHFFFAOYSA-N tris(3,5-dichloro-2-methoxyphenyl)borane Chemical compound COC1=C(Cl)C=C(Cl)C=C1B(C=1C(=C(Cl)C=C(Cl)C=1)OC)C1=CC(Cl)=CC(Cl)=C1OC MSAPLRJYZBZUIZ-UHFFFAOYSA-N 0.000 description 1
- GPCIIHAARKQHKK-UHFFFAOYSA-N tris(3,5-dichloro-2-methylphenyl)borane Chemical compound CC1=C(Cl)C=C(Cl)C=C1B(C=1C(=C(Cl)C=C(Cl)C=1)C)C1=CC(Cl)=CC(Cl)=C1C GPCIIHAARKQHKK-UHFFFAOYSA-N 0.000 description 1
- YITDZFPEFPUBLW-UHFFFAOYSA-N tris(3,5-difluoro-2-methylphenyl)borane Chemical compound CC1=C(F)C=C(F)C=C1B(C=1C(=C(F)C=C(F)C=1)C)C1=CC(F)=CC(F)=C1C YITDZFPEFPUBLW-UHFFFAOYSA-N 0.000 description 1
- DEHCQFBZZXFMHH-UHFFFAOYSA-N tris(3-ethoxy-2,4,5,6-tetrafluorophenyl)borane Chemical compound CCOC1=C(F)C(F)=C(F)C(B(C=2C(=C(OCC)C(F)=C(F)C=2F)F)C=2C(=C(OCC)C(F)=C(F)C=2F)F)=C1F DEHCQFBZZXFMHH-UHFFFAOYSA-N 0.000 description 1
- OZRFIWWJMLPWMZ-UHFFFAOYSA-N tris(3-ethoxy-2,4,6-trifluorophenyl)borane Chemical compound CCOC1=C(F)C=C(F)C(B(C=2C(=C(OCC)C(F)=CC=2F)F)C=2C(=C(OCC)C(F)=CC=2F)F)=C1F OZRFIWWJMLPWMZ-UHFFFAOYSA-N 0.000 description 1
- RWJKXPALZRFLGA-UHFFFAOYSA-N tris(3-ethoxy-2,5,6-trifluorophenyl)borane Chemical compound CCOC1=CC(F)=C(F)C(B(C=2C(=C(OCC)C=C(F)C=2F)F)C=2C(=C(OCC)C=C(F)C=2F)F)=C1F RWJKXPALZRFLGA-UHFFFAOYSA-N 0.000 description 1
- HKWIMMQSMYAAKO-UHFFFAOYSA-N tris(3-ethoxy-2,6-difluorophenyl)borane Chemical compound CCOC1=CC=C(F)C(B(C=2C(=C(OCC)C=CC=2F)F)C=2C(=C(OCC)C=CC=2F)F)=C1F HKWIMMQSMYAAKO-UHFFFAOYSA-N 0.000 description 1
- KTIXVYRZWQMTJX-UHFFFAOYSA-N tris(3-ethyl-2,4,5,6-tetrafluorophenyl)borane Chemical compound CCC1=C(F)C(F)=C(F)C(B(C=2C(=C(CC)C(F)=C(F)C=2F)F)C=2C(=C(CC)C(F)=C(F)C=2F)F)=C1F KTIXVYRZWQMTJX-UHFFFAOYSA-N 0.000 description 1
- JNIHSQJHJRCRIZ-UHFFFAOYSA-N tris(3-ethyl-2,4,6-trifluorophenyl)borane Chemical compound CCC1=C(F)C=C(F)C(B(C=2C(=C(CC)C(F)=CC=2F)F)C=2C(=C(CC)C(F)=CC=2F)F)=C1F JNIHSQJHJRCRIZ-UHFFFAOYSA-N 0.000 description 1
- NQXWZWIBTXCYML-UHFFFAOYSA-N tris(3-ethyl-2,6-difluorophenyl)borane Chemical compound CCC1=CC=C(F)C(B(C=2C(=C(CC)C=CC=2F)F)C=2C(=C(CC)C=CC=2F)F)=C1F NQXWZWIBTXCYML-UHFFFAOYSA-N 0.000 description 1
- YMJKRXSLSCKFCB-UHFFFAOYSA-N tris(4-ethoxy-2,3,5,6-tetrafluorophenyl)borane Chemical compound FC1=C(F)C(OCC)=C(F)C(F)=C1B(C=1C(=C(F)C(OCC)=C(F)C=1F)F)C1=C(F)C(F)=C(OCC)C(F)=C1F YMJKRXSLSCKFCB-UHFFFAOYSA-N 0.000 description 1
- WPZPSVBFSFHEKK-UHFFFAOYSA-N tris(4-ethoxy-2,6-difluorophenyl)borane Chemical compound FC1=CC(OCC)=CC(F)=C1B(C=1C(=CC(OCC)=CC=1F)F)C1=C(F)C=C(OCC)C=C1F WPZPSVBFSFHEKK-UHFFFAOYSA-N 0.000 description 1
- HHAXDJVVCGROSF-UHFFFAOYSA-N tris(4-ethyl-2,3,5,6-tetrafluorophenyl)borane Chemical compound FC1=C(F)C(CC)=C(F)C(F)=C1B(C=1C(=C(F)C(CC)=C(F)C=1F)F)C1=C(F)C(F)=C(CC)C(F)=C1F HHAXDJVVCGROSF-UHFFFAOYSA-N 0.000 description 1
- GUAUIVZHYGSJCQ-UHFFFAOYSA-N tris(4-ethyl-2,3,6-trifluorophenyl)borane Chemical compound FC1=C(F)C(CC)=CC(F)=C1B(C=1C(=C(F)C(CC)=CC=1F)F)C1=C(F)C=C(CC)C(F)=C1F GUAUIVZHYGSJCQ-UHFFFAOYSA-N 0.000 description 1
- QFALBOXDYQNACI-UHFFFAOYSA-N tris(5-ethoxy-2,4-difluorophenyl)borane Chemical compound C1=C(F)C(OCC)=CC(B(C=2C(=CC(F)=C(OCC)C=2)F)C=2C(=CC(F)=C(OCC)C=2)F)=C1F QFALBOXDYQNACI-UHFFFAOYSA-N 0.000 description 1
- BJMVYDYEVJOARO-UHFFFAOYSA-N tris(5-ethyl-2,4-difluorophenyl)borane Chemical compound C1=C(F)C(CC)=CC(B(C=2C(=CC(F)=C(CC)C=2)F)C=2C(=CC(F)=C(CC)C=2)F)=C1F BJMVYDYEVJOARO-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/027—Organoboranes and organoborohydrides
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Description
で示されるアリールホウ素化合物を含む溶液に、安定化剤として、前記アリールホウ素化合物に対して水より親和性の高い化合物を配合することを特徴とする。
式(1):
で示されるアリールホウ素化合物と、安定化剤として、前記アリールホウ素化合物に対して水より親和性の高い化合物を含むことを特徴とする。
前記アリールホウ素化合物は、好ましくは、式(1):
で示されるアリールホウ素化合物である。
前記安定化剤としては、好ましくは、式(2):
で示されるエーテル系化合物が用いられる。
本発明の方法により安定化されるアリールホウ素化合物は、式(1):
で示される。その製造法は特に限定されるものではなく、従来公知のいかなる方法により製造してもよい。アリールホウ素化合物は、例えば、対応するアリールマグネシウム誘導体またはアリールリチウム誘導体とハロゲン化ホウ素とを、例えば、エーテル系溶媒中で反応させることにより得ることができる。あるいは、アリールホウ素化合物は、自ら製造することなく、市販品など、他者から供給されるものを用いてもよい。
で示される3個以上、8個以下の酸素原子を含むクラウンエーテル環などが挙げられる。複素環が置換されている場合、置換基はハロゲン原子、アルキル基およびアルコキシ基から選択される少なくとも1種である。置換基となりうるハロゲン原子、アルキル基およびアルコキシ基としては、Ar1、Ar2またはAr3で示される置換アリール基の置換基として上記したものと同様のハロゲン原子、アルキル基およびアルコキシ基が挙げられる。
19F−NMRの測定試料は、保存中の溶液の一部を抜き取り、窒素雰囲気下、この溶液にCDCl3を混合することにより調製した。19F−NMRスペクトルは、所定の条件下で測定した。
本実施例では、炭化水素系溶媒であるメチルシクロヘキサンとトルエンとの混合溶媒中にアリールホウ素化合物であるトリス(ペンタフルオロフェニル)ボランを含む溶液に安定化剤であるジエチルエーテルを配合することにより、トリス(ペンタフルオロフェニル)ボランの保存安定性を調べた。
本実施例では、炭化水素系溶媒であるメチルシクロヘキサンとトルエンとの混合溶媒中にアリールホウ素化合物であるトリス(ペンタフルオロフェニル)ボランを含む溶液に安定化剤である1,2−ジメトキシエタンを配合することにより、トリス(ペンタフルオロフェニル)ボランの保存安定性を調べた。
本実施例では、炭化水素系溶媒であるメチルシクロヘキサンとトルエンとの混合溶媒中にアリールホウ素化合物であるトリス(ペンタフルオロフェニル)ボランを含む溶液に安定化剤である1,2−ジメトキシエタンを配合することにより、トリス(ペンタフルオロフェニル)ボランの保存安定性を調べた。
本実施例では、炭化水素系溶媒であるメチルシクロヘキサンとトルエンとの混合溶媒中にアリールホウ素化合物であるトリス(ペンタフルオロフェニル)ボランを含む溶液に安定化剤である1,2−ジメトキシエタンを配合することにより、トリス(ペンタフルオロフェニル)ボランの保存安定性を調べた。
本実施例では、炭化水素系溶媒であるメチルシクロヘキサンとトルエンとの混合溶媒中にアリールホウ素化合物であるトリス(ペンタフルオロフェニル)ボランを含む溶液に安定化剤であるジイソプロピルエーテルを配合することにより、トリス(ペンタフルオロフェニル)ボランの保存安定性を調べた。
本比較例では、炭化水素系溶媒であるメチルシクロヘキサンとトルエンとの混合溶媒中にアリールホウ素化合物であるトリス(ペンタフルオロフェニル)ボランを含む溶液に安定化剤を配合することなく、トリス(ペンタフルオロフェニル)ボランの保存安定性を調べた。
Claims (4)
- 炭化水素系溶媒中に式(1):
[式中、Ar1、Ar2およびAr3は、互いに独立して、置換もしくは無置換のアリール基を表す;ここで、アリール基が置換されている場合、置換基はハロゲン原子、アルキル基およびアルコキシ基から選択される少なくとも1種である]
で示されるアリールホウ素化合物を含む溶液またはスラリーに、安定化剤として、式(2):
[式中、R 1 およびR 2 は、互いに独立して、アルキル基、アルコキシアルキル基、または置換もしくは無置換のアリール基を表すか、あるいは、互いに結合して、隣接する酸素原子と共に、置換もしくは無置換の含酸素複素環を形成していてもよい;ここで、アリール基が置換されている場合、および/または、含酸素複素環が置換されている場合、置換基はハロゲン原子、アルキル基およびアルコキシ基から選択される少なくとも1種である]
で示されるエーテル系化合物を配合することを特徴とするアリールホウ素化合物の安定化方法。 - 炭化水素系溶媒中に、式(1):
[式中、Ar1、Ar2およびAr3は、互いに独立して、置換もしくは無置換のアリール基を表す;ここで、アリール基が置換されている場合、置換基はハロゲン原子、アルキル基およびアルコキシ基から選択される少なくとも1種である]
で示されるアリールホウ素化合物と、安定化剤として、式(2):
[式中、R 1 およびR 2 は、互いに独立して、アルキル基、アルコキシアルキル基、または置換もしくは無置換のアリール基を表すか、あるいは、互いに結合して、隣接する酸素原子と共に、置換もしくは無置換の含酸素複素環を形成していてもよい;ここで、アリール基が置換されている場合、および/または、含酸素複素環が置換されている場合、置換基はハロゲン原子、アルキル基およびアルコキシ基から選択される少なくとも1種である]
で示されるエーテル系化合物を含むことを特徴とするアリールホウ素化合物の安定化組成物。
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JP2005021556A JP4630078B2 (ja) | 2005-01-28 | 2005-01-28 | アリールホウ素化合物の安定化方法および安定化組成物 |
PCT/JP2006/301598 WO2006080538A1 (en) | 2005-01-28 | 2006-01-25 | Stabilizing method and stabilized composition for aryl boron compounds |
EP06712741.5A EP1817318B1 (en) | 2005-01-28 | 2006-01-25 | Stabilizing method and stabilized composition for aryl boron compounds |
US11/883,164 US20080154065A1 (en) | 2005-01-28 | 2006-01-25 | Stabilizing Method and Stabilized Composition for Aryl Boron Compounds |
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JP2007055917A (ja) * | 2005-08-23 | 2007-03-08 | Nippon Shokubai Co Ltd | ボラジン化合物の保存方法およびボラジン化合物保存用容器 |
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RU2159246C2 (ru) * | 1996-02-28 | 2000-11-20 | Ниппон Сокубаи Ко., Лтд. | Способ получения фторарилмагниевого производного и способ получения (фторарил) боранового соединения (варианты) |
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JP2007055917A (ja) * | 2005-08-23 | 2007-03-08 | Nippon Shokubai Co Ltd | ボラジン化合物の保存方法およびボラジン化合物保存用容器 |
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US20080154065A1 (en) | 2008-06-26 |
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