Conditions | Yield |
---|---|
With water In water byproducts: Cl2; Cl2 removed by CO2 before hydrolysis completed;; | A n/a B n/a C 30% |
ruthenium(IV) chloride
A
nitrogen
B
ruthenium(III)chloride
C
sodium chloride
Conditions | Yield |
---|---|
In hydrogenchloride | |
In hydrogenchloride |
ruthenium(III)chloride
Conditions | Yield |
---|---|
In neat (no solvent) 140°C, 48 h; | |
In neat (no solvent) drying under vacuum at 125°C for 15 h; | |
With thionyl chloride In neat (no solvent) refluxed for 2 h; |
H(1+)*{Ru(H2O)2Cl4}(1-)=H{Ru(H2O)2Cl4}
ruthenium(III)chloride
Conditions | Yield |
---|---|
In not given heating;; pure RuCl3 obtained;; |
H(1+)*{Ru(H2O)2Cl4}(1-)=H{Ru(H2O)2Cl4}
ruthenium(III)chloride
Conditions | Yield |
---|---|
In not given heating;; pure RuCl3 obtained;; |
Conditions | Yield |
---|---|
In not given fuming off with HCl;; impure RuCl3 obtained;; | |
In neat (no solvent) dried air-free HCl; at 105 °C;; |
ruthenium
ruthenium(III)chloride
Conditions | Yield |
---|---|
In neat (no solvent) chlorination of specially prepd., finely divided Ru at 800 °C;; | |
With chlorine | |
In neat (no solvent) chlorination of specially prepd., finely divided Ru at 800 °C;; | |
With chlorine |
Conditions | Yield |
---|---|
In neat (no solvent) at 400 °C;; RuCl3 free from carbon;; | |
In neat (no solvent) at 400 °C;; carbon-free RuCl3 obtained;; |
Conditions | Yield |
---|---|
In neat (no solvent) finely dispersed Ru;; | |
With carbon monoxide In neat (no solvent) at 600-800 °C;; may contain RuCl2*2CO;; | |
With carbon monoxide In neat (no solvent) passing a stream of carefully dried Cl2 and CO over powdered Ru in a glass tube at 700-800 °C; air excluded;; crystn. after cooling down in a Cl2 stream;; |
chlorine
ruthenium
A
ruthenium(IV) chloride
B
ruthenium(III)chloride
Conditions | Yield |
---|---|
In neat (no solvent) react. of Ru in a stream of Cl2; react. of formed RuCl3 with Cl2 forming volatile RuCl4; decompn. of RuCl4 on cooling;; |
Conditions | Yield |
---|---|
In neat (no solvent) chlorination of Ru at 600-700 °C in SiO2 vessels;; formation of Ru2OCl6 as by-product;; |
Conditions | Yield |
---|---|
In not given soln. evapd. at 180 °C under a well dried HCl stream;; product contains 0.04% H;; | |
In neat (no solvent) byproducts: H2O; dry educts; at 105-115 °C;; | |
In not given concd. HCl;; |
ruthenium(III)chloride
Conditions | Yield |
---|---|
heating in Cl2 atmosphere at 600°C; elem. anal.; X-ray diffraction, thermogravimetric and differential thermal anal.; |
Conditions | Yield |
---|---|
With carbon monoxide In neat (no solvent) passing the gas stream over RuO2 at red heat;; |
ruthenium(III)chloride
Conditions | Yield |
---|---|
With carbon monoxide; chlorine In neat (no solvent) | |
With CO; Cl2 In neat (no solvent) |
Conditions | Yield |
---|---|
In neat (no solvent) |
Conditions | Yield |
---|---|
In neat (no solvent) heating to 440 °C in a CO2 atmosphere or in vac.;; |
ruthenium(III)chloride
Conditions | Yield |
---|---|
With alc. In not given heating;; | |
With tin(ll) chloride In not given |
ruthenium tetroxide
ruthenium(III)chloride
Conditions | Yield |
---|---|
With hydrogenchloride In not given in concd. HCl;; | |
With HCl In not given in concd. HCl;; |
ruthenium(IV) chloride
ruthenium(III)chloride
Conditions | Yield |
---|---|
In not given in presence of KI;; | >99 |
With hydrogenchloride In not given byproducts: Cl2; in 15% HCl;; |
Conditions | Yield |
---|---|
In neat (no solvent) irreversible decomposition under pressure rise of 2 Torr into Cl2 and amorphous RuCl3 on warming at -29 to -31°C;; | |
In neat (no solvent) irreversible decomposition under pressure rise of 2 Torr into Cl2 and amorphous RuCl3 on warming at -29 to -31°C;; | |
In neat (no solvent) equilibrum of gasous RuCl4 with solid RuCl3 and gasous Cl2;; |
hydrogen tetrachlorodiaquoruthenate(III)
ruthenium(III)chloride
Conditions | Yield |
---|---|
In neat (no solvent) heating in a HCl stream to 200 °C;; | |
In neat (no solvent) heating in a HCl stream to 200 °C;; |
ruthenium(V) fluoride
ruthenium(III)chloride
Conditions | Yield |
---|---|
With dichloromethane In dichloromethane byproducts: CHCl2F, HF, CH2ClF; inert atmosphere; excess of CH2Cl2, warming to room temp.; further byproducts; |
Conditions | Yield |
---|---|
In neat (no solvent) loss of 2 mol H2O on heating at 100 °C or at 25 °C in vac. forming a pink product; further loss of 2 mol H2O at 120-150 °C forming a brick-red product that becomes brown at 360 °C; at 440 °C in vac complete decompn.;; formation of RuCl3, RuO2 and CO2;; |
ruthenium(III)chloride
dicarbonyldichlororuthenium(II)
Conditions | Yield |
---|---|
With CO In 2-methoxy-ethanol RuCl3 dissolved in 2-methoxyethanol, soln. heated at reflux as stream of CO passed into it for 170-210 min; solvent removed at reduced pressure; | 100% |
potassium hexafluorophosphate
5,5'-bis(3-octylthienyl)-2,2'-pyridine
ruthenium(III)chloride
Conditions | Yield |
---|---|
In ethylene glycol under Ar atm. ethyleneglycol soln. RuCl3 and tpbpy was refluxed at 180°C for 2 h, solvent was removed in vacuo, residue was purified by chromy. on silica using acetone/water/sat.aq.KNO3 94.3/5.6/0.1 as eluent, KPF6 was added; | 100% |
ruthenium(III)chloride
Conditions | Yield |
---|---|
With sodium hypophosphite In water mixt. (P-salt as reducing agent) refluxing for 40 min, soln. vac. concn., pptn. into acetone; ppt. repptn. from MeOH into acetone twice or three times; elem. anal.; | 99% |
ruthenium(III)chloride
Conditions | Yield |
---|---|
In not given prepn. according to V. A. Emel'yanov et al., Russ. J. Inorg. Chem. 46, 346 (2001); | 97% |
ruthenium(III)chloride
cyclopenta-1,3-diene
bis(η5-cyclopentadienyl)ruthenium
Conditions | Yield |
---|---|
With zinc In ethanol a mixt. of RuCl3 and ethanol was stirred for 2-3 h at 20°C; cyclopentadiene (frehly distd.) was added; Zn powder was added gradually (temp. < 30-35°C); the mixt. was stirred at 20°C for 3-4 d; ppt. filtered off, washed (hot C6H6 on filter); filtrates concd. (vac.), chromd. (SiO2, C6H6); | 95% |
ruthenium(III)chloride
isoprene
Conditions | Yield |
---|---|
In 2-methoxy-ethanol soln. of RuCl3 in a mixt. of isoprene and 2-methoxyethanol was refluxed for 10 d under N2; crystals were filtered, washed with Et2O and dried in vac, elem. anal.; | 95% |
dmap
ruthenium(III)chloride
2,9-di(pyridin-2-yl)-1,10-phenanthroline
Conditions | Yield |
---|---|
In ethanol phenathroline-compound was treated with RuCl3 in refluxing ethanol followed by the introduction of 4-dimethylaminopyridine; | A 5% B 95% |
ruthenium(III)chloride
Conditions | Yield |
---|---|
In water; acetone Ru-Co complex was dissolved in acetone-water and treated with anhydrous RuCl3, after 2 h stirring the solvent was removed; residue was extd. with CH2Cl2, ext. was filtered through silica, filtrate gave on evapn. black-green solid; | 93% |
ruthenium(III)chloride
[(Ru(((bis(3,5-dimethylpyrazol-1-yl)acetate)2]
Conditions | Yield |
---|---|
In methanol RuCl3 (0.24 mmol) was dissolved in MeOH contg. ligand (0.48 mmol) and stirred for 12 h; soln. was evapd. and the liq. was rotoevapd. and extd. several times with an acetone:MeOH (4:1) soln. and evapd. to dryness under vac.; elem. anal.; | 93% |
ruthenium(III)chloride
4′-(4-phenylphenyl)-2,2′:6′,2″-terpyridine
Ru(4′-biphenyl-2,2′:6′,2″-terpyridine)Cl3
Conditions | Yield |
---|---|
In ethanol ligand and RuCl3 in EtOH were heated at reflux for 1 h; cooled, ppt. filtered off, washed with ice-cold EtOH; | 92% |
ruthenium(III)chloride
Conditions | Yield |
---|---|
In methanol RuCl3 (0.24 mmol) was dissolved in MeOH contg. ligand (0.24 mmol) and stirred for 12 h; soln. was evapd. and the liq. was rotoevapd. and extd. several times with an acetone:MeOH (4:1) soln. and evapd. to dryness under vac.; elem. anal.; | 92% |
ruthenium(III)chloride
2,6-bis(1-methyl-1H-benzo[d]imidazol-2-yl)pyridine
Conditions | Yield |
---|---|
In ethanol equimolar amts.; refluxing under Ar in dark for 1 h; cooling to 25°C, collection (filtration), washing (EtOH), drying (vac.); elem. anal.; | 92% |
ruthenium(III)chloride
[(Ru(((bis(3,5-dimethylpyrazol-1-yl)methane sulfonate)2]
Conditions | Yield |
---|---|
In methanol RuCl3 (0.24 mmol) was dissolved in MeOH contg. ligand (0.48 mmol) and stirred for 12 h; soln. was evapd. and the liq. was rotoevapd. and extd. several times with an acetone:MeOH (4:1) soln. and evapd. to dryness under vac.; elem. anal.; | 91% |
Conditions | Yield |
---|---|
With KHCO3 In further solvent(s) (inert atm.); reaction of ruthenium compd. with methanol-(13)C in presecnce of phosphine deriv. and KHCO3; Marchenko A.V., Huffman J.C., ValergaP., Jimenez Tenorio M., Puerta M.C., Caulton K.G., Inorg. Chem., 2001, 40, 6444; | 91% |
potassium nitrite
ruthenium(III)chloride
Conditions | Yield |
---|---|
With Na(1+); Cl2 In hydrogenchloride heating on a water bath for 30 min; filtn. and dissolving in a minimum of water; elem. anal.; | 90% |
carbon monoxide
ruthenium(III)chloride
dodecacarbonyl-triangulo-triruthenium
Conditions | Yield |
---|---|
With caesium carbonate In methanol other Radiation; mixt. of RuCl3, Cs2CO3 and MeOH was sealed in microwave app.; CO (50 psi) was introduced; sealed; heated with stirring to 110°C using power of 300 W; held for 10 min; cooled to 50°C; evapd. (vac.); hexane added; heated; solvent removed; | 90% |
With Cu or Zn In ethanol other Radiation; γ irradiation of 1E-3 mol/l RuCl3 in ethanol under CO atmosphere at room temp. in presence of Cu or Zn powder; | |
With zinc In methanol heating RuCl3 with Zn at a CO pressure of 5-10 atm at 65 °C for 30 h;; extraction of thr solid residue of the filtration; pptn. on concentrating;; | |
With Zn In methanol heating RuCl3 with Zn at a CO pressure of 5-10 atm at 65 °C for 30 h;; extraction of thr solid residue of the filtration; pptn. on concentrating;; |
ruthenium(III)chloride
ethylenediamine
[Ru(((bis(3,5-dimethylpyrazol-1-yl)acetate)(ethylenediamine)(Cl)]
Conditions | Yield |
---|---|
In methanol RuCl3 (0.24 mmol) was dissolved in MeOH contg. ligand (0.24 mmol) and ethylenediamine (0.24 mmol) and stirred for 12 h; soln. was evapd. and the liq. was rotoevapd. and extd. several times with an acetone:MeOH (4:1) soln. and evapd. to dryness under vac.; elem. anal.; | 90% |
ruthenium(III)chloride
[bis(bis(1,3-dimethylpyrazol-1-yl)dithio-κ3-N,N,S-acetate)ruthenium(II)]
Conditions | Yield |
---|---|
In methanol Kinetics; byproducts: LiCl; inert atm., stoich., a soln. of Ru compd. added to a soln. of Li compd. (4 portions), stirred for 4 h; solvent removed, dissolved (CH2Cl2), filtered, solvent removed (vac.); elem. anal.; | 90% |
5-chlorosalicylaldehyde thiosemicarbazone
water
ruthenium(III)chloride
Conditions | Yield |
---|---|
In methanol soln. of RuCl3 mixed with soln. of Schiff base (molar ratio 1:2), mixt. stirred under reflux for 1 h; ppt. septd. by filtration, washed (CH3OH), dried over P4O10; elem. anal.; | 90% |
ruthenium(III)chloride
Conditions | Yield |
---|---|
In methanol RuCl3 (0.24 mmol) was dissolved in MeOH contg. ligand (0.24 mmol) and stirred for 12 h; soln. was evapd. and the liq. was rotoevapd. and extd. several times with an acetone:MeOH (4:1) soln. and evapd. to dryness under vac.; elem. anal.; | 90% |
4'-(p-decyloxyphenyl)terpyridine
ruthenium(III)chloride
[(4'-(p-decyloxyphenylyl)terpyridine)RuCl3]
Conditions | Yield |
---|---|
In ethanol 1:1 mixt. refluxed; | 90% |
ruthenium(III)chloride
Conditions | Yield |
---|---|
In not given prepn. according to V. A. Emel'yanov et al., Russ. J. Inorg. Chem., 46, 346 (2001); M. A. Il'in et al., Russ. J. Inorg. Chem. 53, 1070 (2008); | 90% |
2,2':6,2''-terpyridine
ammonium tetrafluroborate
2-(phenylazo)pyridine
ruthenium(III)chloride
sodium nitrite
(nitro-κN)[2-(phenyldiazenyl-κN2)pyridine-κN](2,2':6',2''-terpyridine-κ3N)ruthenium(II) tetrafluoroborate
Conditions | Yield |
---|---|
With AgNO3 In water; acetone byproducts: AgCl; RuCl3, 2,2':6',2''-terpyridine gave trichloro(terpyridine)Ru(III); 2-(phenylazo)pyridine added; soln. intermediate Cl(2-(phenyldiazenyl)pyridine)(terpyridine)Ru(II) chloride, AgNO3 in Me2CO/H2O reflux 15 min; NaNO2 added; 1 h heated; NH4BF4 added; 5 d; filtered off; washed (cool H2O, Et2O); crystn. (MeOH:M2CO = 1:1 v/v); | 88% |
ruthenium(III)chloride
ethylenediamine
[Ru(((bis(3,5-dimethylpyrazol-1-yl)methane sulfonate)(ethylenediamine)(Cl)]
Conditions | Yield |
---|---|
In methanol RuCl3 (0.24 mmol) was dissolved in MeOH contg. ligand (0.24 mmol) and ethylenediamine (0.24 mmol) and stirred for 12 h; soln. was evapd. and the liq. was rotoevapd. and extd. several times with an acetone:MeOH (4:1) soln. and evapd. to dryness under vac.; elem. anal.; | 88% |
2-hydroxy-1-naphthaldehydethiosemicarbazone
water
ruthenium(III)chloride
Conditions | Yield |
---|---|
In methanol soln. of RuCl3 mixed with soln. of Schiff base (molar ratio 1:2), mixt. stirred under reflux for 1 h; ppt. septd. by filtration, washed (CH3OH), dried over P4O10; detd. by elem. anal., ESR; | 87% |
Conditions | Yield |
---|---|
With HCl In hydrogenchloride; methanol; dimethyl sulfoxide heating mixt. of ruthenium compd., bipyridine deriv., aq. HCl, methanol and DMSO at 85°C for 1 wk; addn. of methanol, keeping at room temp. for 2 d, filtration, washing with ethanol and diethyl ether, drying at room temp., elem. anal.; | 87% |
With HOOCC5H3NC5H3N(COOH); HCl In hydrogenchloride; methanol; dimethyl sulfoxide heating mixt. of ruthenium compd., bipyridine deriv., aq. HCl, methanol and DMSO at 65°C for 1 wk; isolation of crystals, elem. anal.; | 8.9% |
ruthenium(III)chloride
ethylenediamine
[RuCl2((CH2NH2)2)(O3SCH(N2C3H(CH3)2)2)]
Conditions | Yield |
---|---|
In acetonitrile N2, equimol., stirred for 6 h; evapd., extd. (acetone), evapd. to dryness (vac.); elem. anal.; | 87% |
ruthenium(III)chloride
1,10-phenanthroline hydrate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide stoich. amt of N-compd. was added to Ru-compd., reflux for 6 h; solvent was evapd., recrystn. hot water; | 85% |
ruthenium(III)chloride
ethyl (diphenylphosphino)acetate
mer-RuCl3(Ph2PPCH2COOEt)2
Conditions | Yield |
---|---|
In hydrogenchloride; ethanol a soln. of phosphinoacetate in ethanol added slowly to a mixture of RuCl3 in ethanol and aq. HCl; stirred for 15 min; filtered; cooled to -15°C; recrystd. from ethanol/hexane; elem. anal.; | 85% |
2-(2'-pyridyl)benzimidazole
ruthenium(III)chloride
[Ru(C5H4NC7H5N2)2Cl2](1+)*Cl(1-)=[Ru(C5H4NC7H5N2)2Cl2]Cl
Conditions | Yield |
---|---|
In ethanol mixed, degassed, refluxed for 72 h; solvent evapd. (vac), washed with boiling petrolium ether, recrystd. from hot benzene-ethanol; elem. anal.; | 85% |
EPA Genetic Toxicology Program. Reported in EPA TSCA Inventory.
The Ruthenium trichloride, with the CAS registry number 10049-08-8, is also known as Ruthenium(III) chloride. It belongs to the product categories of Inorganics; Catalysts for Organic Synthesis; Classes of Metal Compounds; Homogeneous Catalysts; Ru (Ruthenium) Compounds; Synthetic Organic Chemistry; Titanium Alkoxides, etc. (Homogeneous Catalysts); Transition Metal Compounds; Catalysis and Inorganic Chemistry; Ru Catalysts Metal and Ceramic Science; Ruthenium; Ruthenium Salts; Salts; Metal Halide. Its EINECS registry number is 233-167-5. This chemical's molecular formula is Cl3Ru and molecular weight is 207.43. What's more, its systematic name is called Ruthenium(+2) cation trichloride. It should be stored in a cool, dry and well-ventilated place. Crystalline material is usually prepared by heating powdered ruthenium metal to 700 °C under a 4:1 mixture of chlorine and carbon monoxide: the product is carried by the gas stream and crystallises upon cooling.
Physical properties about Ruthenium trichloride are: (1)#H bond acceptors: 0; (2)#H bond donors: 0; (3)#Freely Rotating Bonds: 0; (4)Polar Surface Area: Å2.
Uses of Ruthenium trichloride: it is used to produce other chemicals. For example, RuCl3(H2O)x reacts with carbon monoxide under mild conditions. Reduction of carbonylated solutions with Zn affords the orange triangular cluster [Ru3(CO)12].
3 RuCl3·xH2O + 4.5 Zn + 12 CO (high pressure) → Ru3(CO)12 + 3 H2O + 4.5 ZnCl2
When you are dealing with this chemical, you should be very careful. This chemical may destroy living tissue on contact and may cause burns. it is harmful if swallowed and may cause long-term adverse effects in the aquatic environment. Therefore, you should wear suitable protective clothing, gloves and eye/face protection. In addition, you must avoid releasing to the environment and refer to special instructions/safety data sheet. In case of contacting with eyes, you should rinse immediately with plenty of water and seek medical advice. And in case of accident or if you feel unwell seek medical advice immediately.
You can still convert the following datas into molecular structure:
(1) SMILES: [Ru+2].[Cl-].[Cl-].[Cl-]
(2) InChI: InChI=1S/3ClH.Ru/h3*1H;/q;;;+2/p-3
(3) InChIKey: SJBXHTJATUAXJN-UHFFFAOYSA-K
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
rat | LD50 | intraperitoneal | 360mg/kg (360mg/kg) | Environmental Quality and Safety, Supplement. Vol. 1, Pg. 1, 1975. |
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