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[Ru(CO)(PCy3)2Cl2] is a ruthenium-based organometallic complex, featuring a ruthenium (Ru) center coordinated to a carbonyl (CO) ligand, two phosphine ligands with cyclohexyl groups (PCy3), and two chloride (Cl) ligands. [Ru(CO)(PCy3)2Cl2] is of interest in various fields, including homogeneous catalysis, where it can serve as a precursor to other catalytically active species. The cyclohexyl groups on the phosphine ligands provide steric bulk, which can influence the reactivity and selectivity of the complex in catalytic reactions. The chloride ligands can be replaced or activated, allowing for the formation of new bonds and the initiation of catalytic cycles. Overall, [Ru(CO)(PCy3)2Cl2] is a versatile starting material in the synthesis of ruthenium complexes with potential applications in catalysis and other areas of chemistry.

52524-94-4

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52524-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52524-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,2 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52524-94:
(7*5)+(6*2)+(5*5)+(4*2)+(3*4)+(2*9)+(1*4)=114
114 % 10 = 4
So 52524-94-4 is a valid CAS Registry Number.

52524-94-4Relevant academic research and scientific papers

Multifunctional ruthenium catalysts: A novel borohydride-stabilized polyhydride complex containing the basic, chelating diphosphine 1,4-bis(dicyclohexylphosphino)butane and its application to hydrogenation and Murai catalysis

Drouin, Samantha D.,Amoroso, Dino,Yap, Glenn P.A.,Fogg, Deryn E.

, p. 1042 - 1049 (2002)

[RuCl2(dcypb)(CO)]2 2 (dcypb = 1,4-bis(dicyclohexylphosphino)butane) was prepared in high yield via phosphine exchange between dcypb and RuCl2(CO)PPh3)2(DMF) (1). Reaction of 2 with 8 equiv of KBHsBu3 affords [fac-RuH3(CO)(dcypb)]- (3), stabilized by interactions with a K+ counterion and an intact KBHsBu3 molecule in the third coordination sphere. Substantial ion pairing accounts for the stability and high hydrocarbon solubility of 3. Complex 3 effects reduction of benzophenone under unprecedentedly mild conditions, at 1 atm of H2 in refluxing 2-propanol. It is also active for ortho functionalization of benzophenone under 20 atm of ethylene. Stoichiometric experiments reveal facile formation of orthometalated RuH(CO)[OC(C6H4)(Ph)](dcypb) (5), an intermediate proposed in both types of catalysis. The catalytic activity of isolated 5 supports this hypothesis in the case of hydrogenation but not of Murai catalysis. The X-ray crystal structures of 3 and 5 are reported.

Deactivation of the grubbs carbene complex [RuCl2(=CHPh)(PCy3)2] by allylic alcohols

Werner, Helmut,Gruenwald, Claus,Stueer, Wolfram,Wolf, Justin

, p. 1558 - 1560 (2003)

The reactivity of Grubbs-type ruthenium carbenes toward allyl alcohol and its methyl derivative was investigated. It was observed that two distinct pathways for the conversion of the thermally labile hydroxymethylcarbene complex exist. It was also concluded that the required complexes cannot be prepared by the Fischer methodology, since the primary intermediate formed on this route with a metal-formyl bond was usually unstable.

Two generalizable routes to terminal carbido complexes

Caskey, Stephen R.,Stewart, Michael H.,Kivela, Jonathon E.,Sootsman, Joseph R.,Johnson, Marc J. A.,Kampf, Jeff W.

, p. 16750 - 16751 (2007/10/03)

Desulfurization of the thiocarbonyl ligand in square pyramidal [Ru(CS)Cl2(PCy3)2] (1-S) via sulfur atom abstraction using [Mo(H)(η2-Me2CNAr)(N[i-Pr]Ar)2] forms [Ru(C)Cl2(PCy

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