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bis{μ-{η5-(1-phenylborole)}-{η5-(1-phenylborole)}cobalt}ruthenium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111825-63-9

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111825-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111825-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,8,2 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 111825-63:
(8*1)+(7*1)+(6*1)+(5*8)+(4*2)+(3*5)+(2*6)+(1*3)=99
99 % 10 = 9
So 111825-63-9 is a valid CAS Registry Number.

111825-63-9Downstream Products

111825-63-9Relevant academic research and scientific papers

DERIVATE DES BOROLS VIII. (η5-BOROL)COBALT-KOMPLEXE

Herberich, G. E.,Hessner, B.,Saive, R.

, p. 9 - 28 (2007/10/02)

A large variety of (η5-borole)cobalt complexes have been prepared starting with μ-(CO)25-C4H4BR)>2(Co-Co) (IIIa: R = Me, IIIb: R = Ph), including inter alia, the sandwich complexes CpCo(η5-C4H4BR) (VIIa, b), the triple-decked complexes μ-(η5-C4H4BR)5-C4H4BR)>2 (VIIIa, b) and μ-(η5-C4H4BR)(FeCp)5-C4H4BR)> (X, R = Ph), the dinuclear complex μ-(CO)25-C4H4BPh)>(Fe-Co) (IX), and salts M5-C4H4BR)2> (XVa, b: M = Na; XVIa, b: M = NMe4; XVII: M = Cs, R = Ph).The anions 5-C4H4BR)2>(-) readily undergo stacking reactions to form multiple-decked complexes such as the triple-decked compounds μ-(η5-C4H4BR)(5-C4H4BR)> (XIIa, b), μ-(η5-C4H4BR)>5-C4H4BR)> (XVIII), 5-C4H4BPh)5-C4H4BPh)>> (XX), and the quadruple-decker complex Ru5-C4H4BR)Co(η5-C4H4BR)>2 (XXI).The monofacially bound η5-borole ligands in VIIb and VIIIb sohw regiospecific H/D exchange, at the α position of the boron, on treatment with CF3CO2D at room temperature.VIIb undergoes a Friedel-Crafts substitution to give the 2-acetyl derivative XXIV with MeCOCl/SnCl4 in CH2Cl2 at room temperature.The structure of VIIIa, as determined by X-ray diffraction studies is that of a typical triple-decker compound with nearly coplanar rings.The three borole rings form a helix with torsional angles of 59.8 and 72.2 degree.All intra-ring bond distances of the central ligand are longer than those of the outer ligands.The metal-ligand interaction is somewhat stronger for the outer ligands than for the central ligand.

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