JP2004514554A5 - - Google Patents
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- Publication number
- JP2004514554A5 JP2004514554A5 JP2002545827A JP2002545827A JP2004514554A5 JP 2004514554 A5 JP2004514554 A5 JP 2004514554A5 JP 2002545827 A JP2002545827 A JP 2002545827A JP 2002545827 A JP2002545827 A JP 2002545827A JP 2004514554 A5 JP2004514554 A5 JP 2004514554A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- active hydrogen
- antimony
- anion
- temperature
- 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
Links
- 150000001875 compounds Chemical class 0.000 description 13
- 239000000203 mixture Substances 0.000 description 9
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- 150000001450 anions Chemical group 0.000 description 7
- 229910052787 antimony Inorganic materials 0.000 description 7
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 230000007935 neutral effect Effects 0.000 description 5
- 230000005595 deprotonation Effects 0.000 description 4
- 238000010537 deprotonation reaction Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000002243 precursor Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 2
- -1 And n is 1 to 4) Chemical class 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2000/042398 WO2002043861A1 (en) | 2000-11-30 | 2000-11-30 | Novel antimony catalyst compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004514554A JP2004514554A (ja) | 2004-05-20 |
| JP2004514554A5 true JP2004514554A5 (enExample) | 2008-01-31 |
Family
ID=21742213
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002545827A Pending JP2004514554A (ja) | 2000-11-30 | 2000-11-30 | 新規なアンチモン触媒組成物 |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP1341607B1 (enExample) |
| JP (1) | JP2004514554A (enExample) |
| KR (1) | KR100757700B1 (enExample) |
| CN (1) | CN1199731C (enExample) |
| AU (2) | AU2001247096B2 (enExample) |
| DE (1) | DE60031311T2 (enExample) |
| MX (1) | MXPA03004882A (enExample) |
| WO (1) | WO2002043861A1 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4257424B2 (ja) * | 2004-03-09 | 2009-04-22 | 独立行政法人産業技術総合研究所 | フッ素化反応用触媒 |
| WO2012134849A1 (en) | 2011-03-31 | 2012-10-04 | Dow Global Technologies Llc | Method for producing short-chain polyfunctional polyether polyols utilizing superacid and double-metal cyanide catalysis |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3678120A (en) * | 1970-01-29 | 1972-07-18 | Universal Oil Prod Co | Hydrocarbon conversion catalyst and process |
| DE2300248A1 (de) * | 1973-01-04 | 1974-08-15 | Huels Chemische Werke Ag | Verfahren zur alkoxylierung von alkoholen |
| US3925194A (en) * | 1973-11-21 | 1975-12-09 | Mobil Oil Corp | Hydrocarbon conversion with catalyst of sbf' 5 'on silica |
| US4375564A (en) * | 1981-12-23 | 1983-03-01 | Shell Oil Company | Alkoxylation process |
| US4503161A (en) * | 1984-03-23 | 1985-03-05 | Minnesota Mining And Manufacturing Company | Latent Lewis acid catalyst encapsulated within polymerized cycloaliphatic epoxide and polyhydric alcohol |
| US4503211A (en) * | 1984-05-31 | 1985-03-05 | Minnesota Mining And Manufacturing Co. | Epoxy resin curing agent, process and composition |
| DE3913937A1 (de) * | 1989-04-27 | 1990-10-31 | Hoechst Ag | Verfahren zur reinigung von alkylenoxid-addukten |
| US5391722A (en) * | 1990-03-30 | 1995-02-21 | Olin Corporation | Acid-catalyzed fabrication of precursors for use in making polyols using double metal cyanide catalysts |
| DE4012725A1 (de) * | 1990-04-21 | 1991-10-24 | Hoechst Ag | Verfahren zur herstellung von alkoxylaten mit enger homologenverteilung |
| US5002678A (en) * | 1990-06-29 | 1991-03-26 | Olin Corporation | Lubricants for heat transfer fluids |
| DE4117935A1 (de) * | 1991-05-31 | 1992-12-03 | Hoechst Ag | Verfahren zur herstellung von alkoxylaten mit enger homologenverteilung unter verwendung von antimonpentahalogenid-komplexen als katalysator |
| US5292986A (en) * | 1992-04-20 | 1994-03-08 | Phillips Petroleum Company | Isoparaffin-olefin alkylation catalyst composition and process |
| JPH07227540A (ja) * | 1993-12-22 | 1995-08-29 | Kao Corp | アルコキシル化用触媒、該触媒の製造方法及び該触媒を用いるアルコキシレートの製造方法 |
| US5731369A (en) * | 1996-06-27 | 1998-03-24 | Minnesota Mining And Manufacturing Company | Cold curing epoxy resin formulations comprising amine-free antimony pentafluoride-alcohol complex |
| US5910616A (en) * | 1998-06-22 | 1999-06-08 | Laroche Industries, Inc. | Vapor phase process for preparing fluorinated aliphatic compounds |
-
2000
- 2000-11-30 KR KR1020037007180A patent/KR100757700B1/ko not_active Expired - Fee Related
- 2000-11-30 JP JP2002545827A patent/JP2004514554A/ja active Pending
- 2000-11-30 MX MXPA03004882A patent/MXPA03004882A/es active IP Right Grant
- 2000-11-30 AU AU2001247096A patent/AU2001247096B2/en not_active Ceased
- 2000-11-30 EP EP00992823A patent/EP1341607B1/en not_active Expired - Lifetime
- 2000-11-30 CN CNB008200378A patent/CN1199731C/zh not_active Expired - Fee Related
- 2000-11-30 WO PCT/US2000/042398 patent/WO2002043861A1/en not_active Ceased
- 2000-11-30 DE DE60031311T patent/DE60031311T2/de not_active Expired - Lifetime
- 2000-11-30 AU AU4709601A patent/AU4709601A/xx active Pending
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