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[Ru(CO)(P(C6H5)3)((OC10H6CHN)2C6H4)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

867016-60-2

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867016-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 867016-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,7,0,1 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 867016-60:
(8*8)+(7*6)+(6*7)+(5*0)+(4*1)+(3*6)+(2*6)+(1*0)=182
182 % 10 = 2
So 867016-60-2 is a valid CAS Registry Number.

867016-60-2Downstream Products

867016-60-2Relevant academic research and scientific papers

Synthesis, luminescent, redox and catalytic properties of Ru(II) carbonyl complexes containing 2N2O donors

Naresh Kumar,Ramesh

, p. 1885 - 1892 (2005)

Diamagentic ruthenium(II) complexes [Ru(CO)(B)(L)] (where B = PPh 3, AsPh3, py (or) pip; L = dianion of tetradentate Schiff bases) were synthesized from the reaction of tetradentate Schiff bases derived from 2-hydroxy-1-naphthaldehyde and the appropriate diamines with monomeric metal precursors [RuHCl(CO)(EPh3)2 (B)] (where E = As, B = AsPh3; E = P, B = PPh3, py (or) pip). Elemental analyses and spectral (FT-IR, UV-Vis and 1H NMR) studies of all the new synthesized complexes suggest the presence of an octahedral environment around the Ru(II) ion. All the metal complexes exhibit characteristic MLCT absorption and luminescence bands in the visible region. The luminescence efficiency of the ruthenium(II) complexes was explained based on the ligand environment around the metal ion. Cyclic voltammograms of all the complexes display quasireversible oxidations (RuIII/RuII) in the range 0.76-1.04 V and irreversible reduction peaks (RuII/RuI) in the range -0.70 to -0.95 V. The observed redox potentials vary with respect to the size of the chelate ring of Schiff base ligands. Further, the catalytic activity of complex 1 has been found to be high towards the oxidation of primary and secondary alcohols into their corresponding aldehydes and ketones in the presence of N-methylmorpholine-N-oxide (NMO) as co-oxidant. The formation of high valent RuIVO species as a catalytic intermediate is proposed for the catalytic process.

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