Polyelectrochromism of electronically weakly coupled 4,4′-divinylazoarylene-bridged two Ru(CO)Cl(PiPr3)2 entities
US-11987596-B1 · May 21, 2024 · US
US9266916B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9266916-B2 |
| Application number | US-201414655076-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 20, 2014 |
| Priority date | Jan 21, 2013 |
| Publication date | Feb 23, 2016 |
| Grant date | Feb 23, 2016 |
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The present invention is a method for producing dodecacarbonyl triruthenium (DCR) including a process of carbonylating ruthenium chloride with carbon monoxide, in which an amine is added to a reaction system at 0.8 molar equivalent or more with respect to chlorine of the ruthenium chloride and the carbonylation is conducted at a reaction temperature of 50 to 100° C. and a reaction pressure of 0.2 to 0.9 MPa. According to the present invention, it is possible to produce dodecacarbonyl triruthenium having less residual impurity metals without applying a reaction condition of a high pressure.
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The invention claimed is: 1. A method for producing dodecacarbonyl triruthenium having the following Formula, the method comprising a process of carbonylating ruthenium chloride with carbon monoxide, wherein an amine is added to a reaction system at 0.8 molar equivalent or more with respect to chlorine of the ruthenium chloride and the carbonylation is conducted at a reaction temperature of 50 to 100° C. and a reaction pressure of 0.2 to 0.9 MPa 2. The method for producing dodecacarbonyl triruthenium according to claim 1 , wherein an amine to be added is an amine having 3 to 36 carbon atoms. 3. The method for producing dodecacarbonyl triruthenium according to claim 1 , wherein a reaction time is 10 to 30 hours. 4. The method for producing dodecacarbonyl triruthenium according to claim 1 , wherein ruthenium chloride is a ruthenium chloride solution including ruthenium chloride and an organic solvent, and the organic solvent is methanol, ethanol, propanol and butanol. 5. The method for producing dodecacarbonyl triruthenium according to claim 4 , wherein the organic solvent is an organic solvent having a water content of 5% by mass or less. 6. The method for producing dodecacarbonyl triruthenium according to claim 2 , wherein a reaction time is 10 to 30 hours. 7. The method for producing dodecacarbonyl triruthenium according to claim 2 , wherein ruthenium chloride is a ruthenium chloride solution including ruthenium chloride and an organic solvent, and the organic solvent is methanol, ethanol, propanol and butanol. 8. The method for producing dodecacarbonyl triruthenium according to claim 3 , wherein ruthenium chloride is a ruthenium chloride solution including ruthenium chloride and an organic solvent, and the organic solvent is methanol, ethanol, propanol and butanol.
Ruthenium compounds · CPC title
characterized by the use of precursors specially adapted for ALD · CPC title
Carbonyls · CPC title
from metal carbonyl compounds · CPC title
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