JP2003503561A5 - - Google Patents
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- JP2003503561A5 JP2003503561A5 JP2001506699A JP2001506699A JP2003503561A5 JP 2003503561 A5 JP2003503561 A5 JP 2003503561A5 JP 2001506699 A JP2001506699 A JP 2001506699A JP 2001506699 A JP2001506699 A JP 2001506699A JP 2003503561 A5 JP2003503561 A5 JP 2003503561A5
- Authority
- JP
- Japan
- Prior art keywords
- hydrogen atoms
- group containing
- hydrogen
- group
- halogen
- 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.)
- Pending
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- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 204
- 229910052736 halogen Inorganic materials 0.000 description 36
- 150000002367 halogens Chemical class 0.000 description 36
- 150000003839 salts Chemical class 0.000 description 34
- 238000000034 method Methods 0.000 description 32
- 125000000217 alkyl group Chemical group 0.000 description 30
- 125000003118 aryl group Chemical group 0.000 description 30
- 229910052739 hydrogen Inorganic materials 0.000 description 28
- 239000001257 hydrogen Substances 0.000 description 28
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 28
- 150000001450 anions Chemical class 0.000 description 26
- 125000000707 boryl group Chemical group B* 0.000 description 26
- 125000003545 alkoxy group Chemical group 0.000 description 22
- 125000003277 amino group Chemical group 0.000 description 22
- 150000001875 compounds Chemical class 0.000 description 22
- 229910052711 selenium Inorganic materials 0.000 description 22
- 239000011669 selenium Substances 0.000 description 22
- 229910052717 sulfur Inorganic materials 0.000 description 22
- 229910052714 tellurium Inorganic materials 0.000 description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
- 229910052787 antimony Inorganic materials 0.000 description 16
- 229910052785 arsenic Inorganic materials 0.000 description 16
- 229910052797 bismuth Inorganic materials 0.000 description 16
- 229910052698 phosphorus Inorganic materials 0.000 description 16
- -1 pentadienyl Chemical group 0.000 description 15
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 14
- 229910052757 nitrogen Inorganic materials 0.000 description 14
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical class [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 12
- 150000001768 cations Chemical class 0.000 description 12
- 229910052760 oxygen Inorganic materials 0.000 description 12
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 11
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 10
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 10
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 10
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 10
- 229910052732 germanium Inorganic materials 0.000 description 10
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 10
- 150000004820 halides Chemical class 0.000 description 10
- 239000011574 phosphorus Substances 0.000 description 10
- 238000006116 polymerization reaction Methods 0.000 description 10
- 229910052718 tin Inorganic materials 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 8
- 229910052710 silicon Inorganic materials 0.000 description 8
- 239000010703 silicon Substances 0.000 description 8
- 229960001730 nitrous oxide Drugs 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 6
- 229910052786 argon Inorganic materials 0.000 description 6
- 125000004429 atom Chemical group 0.000 description 6
- 229910052798 chalcogen Inorganic materials 0.000 description 6
- 150000004770 chalcogenides Chemical class 0.000 description 6
- 150000001787 chalcogens Chemical class 0.000 description 6
- 229910052734 helium Inorganic materials 0.000 description 6
- 229910052743 krypton Inorganic materials 0.000 description 6
- 239000012968 metallocene catalyst Substances 0.000 description 6
- 229910052754 neon Inorganic materials 0.000 description 6
- 239000001272 nitrous oxide Substances 0.000 description 6
- 229910052704 radon Inorganic materials 0.000 description 6
- 239000011593 sulfur Substances 0.000 description 6
- 229910052723 transition metal Inorganic materials 0.000 description 6
- 150000003624 transition metals Chemical class 0.000 description 6
- 229910052724 xenon Inorganic materials 0.000 description 6
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 4
- 150000003949 imides Chemical class 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 150000002902 organometallic compounds Chemical class 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- MGWGWNFMUOTEHG-UHFFFAOYSA-N 4-(3,5-dimethylphenyl)-1,3-thiazol-2-amine Chemical compound CC1=CC(C)=CC(C=2N=C(N)SC=2)=C1 MGWGWNFMUOTEHG-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- 229910017855 NH 4 F Inorganic materials 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- PFRUBEOIWWEFOL-UHFFFAOYSA-N [N].[S] Chemical compound [N].[S] PFRUBEOIWWEFOL-UHFFFAOYSA-N 0.000 description 2
- 229910052789 astatine Inorganic materials 0.000 description 2
- RYXHOMYVWAEKHL-UHFFFAOYSA-N astatine atom Chemical compound [At] RYXHOMYVWAEKHL-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 2
- ZWWCURLKEXEFQT-UHFFFAOYSA-N dinitrogen pentaoxide Chemical compound [O-][N+](=O)O[N+]([O-])=O ZWWCURLKEXEFQT-UHFFFAOYSA-N 0.000 description 2
- WFPZPJSADLPSON-UHFFFAOYSA-N dinitrogen tetraoxide Chemical compound [O-][N+](=O)[N+]([O-])=O WFPZPJSADLPSON-UHFFFAOYSA-N 0.000 description 2
- LZDSILRDTDCIQT-UHFFFAOYSA-N dinitrogen trioxide Chemical compound [O-][N+](=O)N=O LZDSILRDTDCIQT-UHFFFAOYSA-N 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- 229910052811 halogen oxide Inorganic materials 0.000 description 2
- 229910000039 hydrogen halide Inorganic materials 0.000 description 2
- 239000012433 hydrogen halide Substances 0.000 description 2
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 150000004715 keto acids Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- GKTNLYAAZKKMTQ-UHFFFAOYSA-N n-[bis(dimethylamino)phosphinimyl]-n-methylmethanamine Chemical compound CN(C)P(=N)(N(C)C)N(C)C GKTNLYAAZKKMTQ-UHFFFAOYSA-N 0.000 description 2
- 229910017464 nitrogen compound Inorganic materials 0.000 description 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical compound N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- 229910052696 pnictogen Inorganic materials 0.000 description 2
- 150000003063 pnictogens Chemical class 0.000 description 2
- 125000002577 pseudohalo group Chemical group 0.000 description 2
- 150000003233 pyrroles Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003573 thiols Chemical class 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- SLZWEMYSYKOWCG-UHFFFAOYSA-N Etacelasil Chemical class COCCO[Si](CCCl)(OCCOC)OCCOC SLZWEMYSYKOWCG-UHFFFAOYSA-N 0.000 description 1
- 235000013842 nitrous oxide Nutrition 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14114199P | 1999-06-25 | 1999-06-25 | |
| US60/141,141 | 1999-06-25 | ||
| US38654699A | 1999-08-31 | 1999-08-31 | |
| US09/386,546 | 1999-08-31 | ||
| PCT/US1999/024233 WO2001000691A1 (en) | 1999-06-25 | 1999-10-14 | Process for the polymerization of olefins; polyolefins, and films and articles produced therefrom |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003503561A JP2003503561A (ja) | 2003-01-28 |
| JP2003503561A5 true JP2003503561A5 (cg-RX-API-DMAC10.html) | 2006-11-30 |
Family
ID=26838826
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001506699A Pending JP2003503561A (ja) | 1999-06-25 | 1999-10-14 | オレフィンの重合方法、新規なポリオレフィン並びにこれから製造したフィルム及び物品 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20020004566A1 (cg-RX-API-DMAC10.html) |
| EP (1) | EP1194459B1 (cg-RX-API-DMAC10.html) |
| JP (1) | JP2003503561A (cg-RX-API-DMAC10.html) |
| CN (1) | CN1174008C (cg-RX-API-DMAC10.html) |
| BR (1) | BR9917391B1 (cg-RX-API-DMAC10.html) |
| CA (1) | CA2377259A1 (cg-RX-API-DMAC10.html) |
| DE (1) | DE69928969T2 (cg-RX-API-DMAC10.html) |
| WO (1) | WO2001000691A1 (cg-RX-API-DMAC10.html) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101113341B1 (ko) | 2002-10-15 | 2012-09-27 | 엑손모빌 케미칼 패턴츠 인코포레이티드 | 올레핀 중합용 다중 촉매 시스템 및 이로부터 제조된중합체 |
| US7223822B2 (en) | 2002-10-15 | 2007-05-29 | Exxonmobil Chemical Patents Inc. | Multiple catalyst and reactor system for olefin polymerization and polymers produced therefrom |
| US7550528B2 (en) | 2002-10-15 | 2009-06-23 | Exxonmobil Chemical Patents Inc. | Functionalized olefin polymers |
| US7541402B2 (en) | 2002-10-15 | 2009-06-02 | Exxonmobil Chemical Patents Inc. | Blend functionalized polyolefin adhesive |
| US7053158B2 (en) | 2003-09-22 | 2006-05-30 | Agency For Science, Technology And Research | Carborane trianion based catalyst |
| US6828395B1 (en) | 2003-10-15 | 2004-12-07 | Univation Technologies, Llc | Polymerization process and control of polymer composition properties |
| US7238756B2 (en) | 2003-10-15 | 2007-07-03 | Univation Technologies, Llc | Polymerization process and control of polymer composition properties |
| US7119153B2 (en) * | 2004-01-21 | 2006-10-10 | Jensen Michael D | Dual metallocene catalyst for producing film resins with good machine direction (MD) elmendorf tear strength |
| JP5325023B2 (ja) * | 2009-05-28 | 2013-10-23 | 三菱重工業株式会社 | 含水固体燃料の乾燥装置及び乾燥方法 |
| US9034685B2 (en) * | 2011-02-11 | 2015-05-19 | Dow Global Technologies Llc | Methodology for forming pnictide compositions suitable for use in microelectronic devices |
| CA2938974C (en) | 2014-02-07 | 2023-08-22 | Gojo Industries, Inc. | Compositions and methods with efficacy against spores and other organisms |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4659685A (en) * | 1986-03-17 | 1987-04-21 | The Dow Chemical Company | Heterogeneous organometallic catalysts containing a supported titanium compound and at least one other supported organometallic compound |
| FR2656315B1 (fr) * | 1989-12-22 | 1992-04-17 | Bp Chemicals Snc | Procede de preparation d'un catalyseur a base de zirconium supporte sur du chlorure de magnesium, et utilisation du catalyseur dans la polymerisation des olefines. |
| US5258475A (en) * | 1991-07-12 | 1993-11-02 | Mobil Oil Corporation | Catalyst systems for polymerization and copolymerization of olefins |
| US5608019A (en) * | 1992-12-28 | 1997-03-04 | Mobil Oil Corporation | Temperature control of MW in olefin polymerization using supported metallocene catalyst |
| AU6596694A (en) * | 1993-06-28 | 1995-01-05 | Union Carbide Chemicals & Plastics Technology Corporation | Use of lewis bases for activity reduction in metallocene catalyzed olefin polymerization process |
| CA2174430A1 (en) * | 1993-11-08 | 1995-05-18 | Subrahmanyam Cheruvu | Process for the polymerization or copolymerization of ethylene |
| US6417299B1 (en) * | 1999-06-07 | 2002-07-09 | Eastman Chemical Company | Process for producing ethylene/olefin interpolymers |
| US6417298B1 (en) * | 1999-06-07 | 2002-07-09 | Eastman Chemical Company | Process for producing ethylene/olefin interpolymers |
-
1999
- 1999-10-14 JP JP2001506699A patent/JP2003503561A/ja active Pending
- 1999-10-14 BR BRPI9917391-3A patent/BR9917391B1/pt not_active IP Right Cessation
- 1999-10-14 CA CA002377259A patent/CA2377259A1/en not_active Abandoned
- 1999-10-14 WO PCT/US1999/024233 patent/WO2001000691A1/en not_active Ceased
- 1999-10-14 DE DE69928969T patent/DE69928969T2/de not_active Expired - Lifetime
- 1999-10-14 EP EP99954976A patent/EP1194459B1/en not_active Expired - Lifetime
- 1999-10-14 CN CNB99817100XA patent/CN1174008C/zh not_active Expired - Lifetime
-
2001
- 2001-08-22 US US09/935,299 patent/US20020004566A1/en not_active Abandoned
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