CA2102631A1 - An improved method for making mo4s4l6 - Google Patents
An improved method for making mo4s4l6Info
- Publication number
- CA2102631A1 CA2102631A1 CA2102631A CA2102631A CA2102631A1 CA 2102631 A1 CA2102631 A1 CA 2102631A1 CA 2102631 A CA2102631 A CA 2102631A CA 2102631 A CA2102631 A CA 2102631A CA 2102631 A1 CA2102631 A1 CA 2102631A1
- Authority
- CA
- Canada
- Prior art keywords
- mo4s4l6
- compound
- improved method
- mo2s4l2
- making
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- 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
- C07F11/00—Compounds containing elements of Groups 6 or 16 of the Periodic System
- C07F11/005—Compounds containing elements of Groups 6 or 16 of the Periodic System compounds without a metal-carbon linkage
Abstract
The present invention provides an improved method for preparing compounds of the formula Mo4S4L6 comprising:
contacting a compound having the formula Mo2S4L2, wherein L is a 1,1-dithioacid ligand, with a reducing agent having a reduction potential sufficient to reduce Mo(V) to lower oxidation states, especially to Mo(III) and Mo(IV), at a temperature and for a time sufficient to form the Mo4S4L6 compound. Preferably, the Mo2S4L2 compound is dissolved in an organic solvent along with the reducing agent and the solution is heated at temperatures above 25 °C, up to the boiling point of the solvent and, more preferably, at temperatures in the range of from about 50 °C to about 250 °C.
contacting a compound having the formula Mo2S4L2, wherein L is a 1,1-dithioacid ligand, with a reducing agent having a reduction potential sufficient to reduce Mo(V) to lower oxidation states, especially to Mo(III) and Mo(IV), at a temperature and for a time sufficient to form the Mo4S4L6 compound. Preferably, the Mo2S4L2 compound is dissolved in an organic solvent along with the reducing agent and the solution is heated at temperatures above 25 °C, up to the boiling point of the solvent and, more preferably, at temperatures in the range of from about 50 °C to about 250 °C.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/703,219 US5099046A (en) | 1991-05-20 | 1991-05-20 | Method for making Mo4 S4 L6 (C-2387) |
US703,219 | 1991-05-20 | ||
PCT/US1992/003864 WO1992021614A1 (en) | 1991-05-20 | 1992-05-08 | AN IMPROVED METHOD FOR MAKING Mo4S4L¿6? |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2102631A1 true CA2102631A1 (en) | 1992-11-21 |
CA2102631C CA2102631C (en) | 2001-02-20 |
Family
ID=24824512
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002102631A Expired - Fee Related CA2102631C (en) | 1991-05-20 | 1992-05-08 | An improved method for making mo4s4l6 |
Country Status (6)
Country | Link |
---|---|
US (1) | US5099046A (en) |
EP (1) | EP0597863B1 (en) |
JP (1) | JP3295705B2 (en) |
CA (1) | CA2102631C (en) |
DE (1) | DE69220952T2 (en) |
WO (1) | WO1992021614A1 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3659598B2 (en) * | 1995-02-15 | 2005-06-15 | 旭電化工業株式会社 | Method for producing sulfurized oxymolybdenum dithiocarbamate |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4483762A (en) * | 1983-07-07 | 1984-11-20 | Atlantic Richfield Company | Hydrocarbon conversion process using molybdenum catalyst |
US4727165A (en) * | 1983-11-18 | 1988-02-23 | Phillips Petroleum Company | Catalytically hydrogenated decomposible molybdenum compounds as oil hydrofining agents |
US4889647A (en) * | 1985-11-14 | 1989-12-26 | R. T. Vanderbilt Company, Inc. | Organic molybdenum complexes |
US4927966A (en) * | 1987-06-04 | 1990-05-22 | The Research Foundation Of State University Of New York | 2-mercaptomethylglutaric acid derivatives |
US4832877A (en) * | 1987-09-28 | 1989-05-23 | Exxon Research And Engineering Company | Tetranuclear sulfido-bridged complex of Cr(III) having a strongly magnetic ground state |
-
1991
- 1991-05-20 US US07/703,219 patent/US5099046A/en not_active Expired - Fee Related
-
1992
- 1992-05-08 WO PCT/US1992/003864 patent/WO1992021614A1/en active IP Right Grant
- 1992-05-08 JP JP50041993A patent/JP3295705B2/en not_active Expired - Fee Related
- 1992-05-08 EP EP92911925A patent/EP0597863B1/en not_active Expired - Lifetime
- 1992-05-08 CA CA002102631A patent/CA2102631C/en not_active Expired - Fee Related
- 1992-05-08 DE DE69220952T patent/DE69220952T2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US5099046A (en) | 1992-03-24 |
JP3295705B2 (en) | 2002-06-24 |
EP0597863A4 (en) | 1994-07-27 |
WO1992021614A1 (en) | 1992-12-10 |
CA2102631C (en) | 2001-02-20 |
DE69220952D1 (en) | 1997-08-21 |
EP0597863B1 (en) | 1997-07-16 |
JPH06507907A (en) | 1994-09-08 |
DE69220952T2 (en) | 1997-12-11 |
EP0597863A1 (en) | 1994-05-25 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
MKLA | Lapsed |