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Carbonyldihydrotris(triphenylphosphine)ruthenium(II)

Base Information Edit
  • Chemical Name:Carbonyldihydrotris(triphenylphosphine)ruthenium(II)
  • CAS No.:25360-32-1
  • Molecular Formula:C55H47OP3Ru
  • Molecular Weight:917.969
  • Hs Code.:28439000
  • European Community (EC) Number:625-484-6
  • Mol file:25360-32-1.mol
Carbonyldihydrotris(triphenylphosphine)ruthenium(II)

Synonyms:25360-32-1;CARBONYLDIHYDROTRIS(TRIPHENYLPHOSPHINE)RUTHENIUM(II);Carbonyldihydrotris(triphenylphosphine)-Ruthenium;Carbonyldihydrotris(triphenylphosphine)ruthenium;Carbonyldihydridotris(triphenylphosphine)ruthenium;Dihydridocarbonyltris(triphenylphosphine)ruthenium;Dihydridotris(triphenylphosphine)ruthenium carbonyl;Ru(PPh3)3(CO)(H)2;AKOS016010032;Carbonyl(dihydrido)tris(triphenylphosphine)-ruthenium(II)

Suppliers and Price of Carbonyldihydrotris(triphenylphosphine)ruthenium(II)
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Carbonyldihydrotris(triphenylphosphine)ruthenium(II)
  • 100mg
  • $ 65.00
  • TCI Chemical
  • Carbonyl(dihydrido)tris(triphenylphosphine)ruthenium(II)
  • 1g
  • $ 109.00
  • TCI Chemical
  • Carbonyl(dihydrido)tris(triphenylphosphine)ruthenium(II)
  • 250mg
  • $ 44.00
  • Strem Chemicals
  • Carbonyl(dihydrido)tris(triphenylphosphine)ruthenium (II), 99%
  • 250mg
  • $ 49.00
  • Strem Chemicals
  • Carbonyl(dihydrido)tris(triphenylphosphine)ruthenium (II), 99%
  • 1g
  • $ 147.00
  • Sigma-Aldrich
  • Carbonyldihydridotris(triphenylphosphine)ruthenium(II)
  • 1g
  • $ 137.00
  • Rare Earth Products
  • Dihyridotris(triphenylphosphine)ruthenium (II) D4478H ? Dihyridotris(triphenylphosphine)ruthenium (II)
  • 5gm
  • $ 281.00
  • Rare Earth Products
  • Dihyridotris(triphenylphosphine)ruthenium (II) D4478H ? Dihyridotris(triphenylphosphine)ruthenium (II)
  • 1gm
  • $ 60.00
  • Matrix Scientific
  • Carbonyl(dihydrido)tris(triphenylphosphine)-ruthenium(II) 95+%
  • 250mg
  • $ 189.00
  • Matrix Scientific
  • Carbonyl(dihydrido)tris(triphenylphosphine)-ruthenium(II) 95+%
  • 1g
  • $ 420.00
Total 67 raw suppliers
Chemical Property of Carbonyldihydrotris(triphenylphosphine)ruthenium(II) Edit
Chemical Property:
  • Appearance/Colour:White to off-white powder 
  • Vapor Pressure:4.74E-05mmHg at 25°C 
  • Melting Point:161-163 °C(lit.) 
  • Boiling Point:360°C at 760 mmHg 
  • Flash Point:181.7°C 
  • PSA:40.77000 
  • LogP:10.12640 
  • Storage Temp.:Refrigerator 
  • Sensitive.:Moisture Sensitive 
  • Water Solubility.:Insoluble in water. 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:9
  • Exact Mass:920.203967
  • Heavy Atom Count:60
  • Complexity:204
Purity/Quality:

99% *data from raw suppliers

Carbonyldihydrotris(triphenylphosphine)ruthenium(II) *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn 
  • Hazard Codes:Xn 
  • Statements: 20/21/22 
  • Safety Statements: 36 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:[H-].[H-].C=O.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.[Ru+2]
  • Uses &bull Catalyst for conversion of 1,4-alkynediols into pyrroles &bull Catalyst for oxidation of primary alcohols to methyl esters &bull Catalyst for rearrangement of oximes to amides &bull Catalyst for C-C coupling via directed C-H activation &bull Cata Carbonyldihydrotris(triphenylphosphine)ruthenium(II) is a catalyst used in the preparation of ruthenium (diphenylphosphino)ethyl)amine complexes pre-catalysts for hydrogenation and dehydrogenation. Catalyst for conversion of 1,4-alkynediols into pyrroles Catalyst for oxidation of primary alcohols to methyl esters Catalyst for rearrangement of oximes to amides Catalyst for C-C coupling via directed C-H activation Catalyst for enyne cyclization
Technology Process of Carbonyldihydrotris(triphenylphosphine)ruthenium(II)

There total 44 articles about Carbonyldihydrotris(triphenylphosphine)ruthenium(II) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With triphenylphosphine; In 2-methoxy-ethanol; A soln. of reagents was heated under reflux for 20 min, cooled in an ice-bath;; ppt. was filtered, wshed with EtOH, H2O, EtOH again, dissolved in CH2Cl2, evapd.;;
DOI:10.1016/S0022-328X(00)93469-7
Guidance literature:
With KOH; In ethanol; soln. of KOH in EtOH added to refluxing suspn. of Ru complex and indenein EtOH under N2, refluxed for 4 h; cooled, filtered, extd. (CH2Cl2), filtered, added MeOH, ppt. filtered after 30 min, washed with MeOH, Et2O, dried in vac.; purified by extn. (acetone), evapd., recrystd. (CH2Cl2/Et2O); elem. anal.;
DOI:10.1016/0022-328X(85)88033-5
Guidance literature:
In methanol; Ar-atmosphere; refluxing for 45 min; cooling, filtration, evapn., extn. (Et2O), addn. of hexane, concn., crystn. on standing, collection (filtration), washing (pentane), drying (vac.); elem. anal.;
DOI:10.1021/om990301l
Refernces Edit

Complexes of the Platinum Metals. Part 33. Synthesis of Some Ruthenium and Osmium Sulphonate Derivatives: X-Ray Crystal Structure of Aqua(carbonyl)bis(toluene-p-sulphonato)bis(triphenylphosphine)ruthenium(II)

10.1039/DT9880000415

The research focuses on the synthesis and characterization of ruthenium and osmium sulphonate complexes, with the aim of exploring the potential of sulphonate anions as leaving groups in platinum metal ligand-substitution reactions. The study successfully prepared a series of new sulphonate complexes, including [M(O,SR),(H,O)(CO)(PPh,),] (M = Ru or Os) and [M(O,SR),(CO),(PPh,),], through reactions involving sulphonic acids with precursors such as [MH,(CO)(PPh,),] in refluxing benzene or toluene. The synthesized complexes were characterized using variable-temperature 'H and 31P-{1H} n.m.r. spectroscopy, which revealed fluxional behavior in solution, and X-ray diffraction methods, which determined the solid-state structures. The findings suggest that the M-O,SR bonds trans to CO are less labile than those trans to PPh, in these complexes. The chemicals used in the process include sulphonic acids (RSO,H with R = CH,, CF,, or C,H,CH,-p), carbonyldihydridotris(triphenylphosphine)-ruthenium and -osmium, tricarbonylbis(triphenylphosphine)ruthenium, dicarbonyldihydridobis(triphenylphosphine)osmium, and tetrahydridotris(triphenylphosphine)osmium, among others.

Chemoselective Ruthenium-Catalyzed C-O Bond Activation: Orthogonality of Nickel- and Palladium-Catalyzed Reactions for the Synthesis of Polyaryl Fluorenones

10.1055/s-0036-1590985

The research explores the development of a new methodology for synthesizing polyaryl fluorenones through ruthenium-catalyzed C–O bond activation and arylation. The study focuses on the selective activation of methoxy and O-carbamoyl-substituted fluorenones, establishing reactions that yield various arylated fluorenones with high efficiency. Key chemicals involved include fluorenones, boronic esters, and ruthenium catalysts such as RuH2(CO)(PPh3)3. The researchers also employed palladium and nickel catalysts to achieve orthogonal reactivity, allowing for the synthesis of 1,4-diaryl and 1,4,8-triaryl fluorenones. The methodology leverages the convenience of starting materials and the potential for application in material science, particularly in the development of optical and electrochemical properties for organic light-emitting devices and liquid crystals.

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