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Osmium, tribromo[(4-methylphenyl)azo]bis(triphenylphosphine)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52620-35-6

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52620-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52620-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,2 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52620-35:
(7*5)+(6*2)+(5*6)+(4*2)+(3*0)+(2*3)+(1*5)=96
96 % 10 = 6
So 52620-35-6 is a valid CAS Registry Number.

52620-35-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Os(PPh3)2Br3(N2-p-C6H4CH3)

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:52620-35-6 SDS

52620-35-6Downstream Products

52620-35-6Relevant academic research and scientific papers

Aryldiazo complexes. Syntheses and reactions of new complexes of osmium and ruthenium

Haymore, Barry L.,Ibers, James A.

, p. 2784 - 2795 (1975)

Aryldiazo complexes, [M(CO)2(NNPh)(PPh3)2][PF6] (M = Os, Ru; Ph = C6H5), have been prepared by allowing diazonium salts to react with M(CO)3(PPh3)2. Infrared spectra of the Ru complex suggest the presence of two isomers both in solution and in the solid state. These complexes react with a variety of coordinating anions (X-), to form MX(CO)2(NNPh)(PPh3)2. The osmium derivatives have ν(NN) near 1455 cm-1, which is the lowest value yet reported for a nonbridging aryldiazo ligand. The first aryldiazo-hydrido complexes, MH(CO)2(NNPh)(PPh3)2 and MH(CO)(NNPh)(PPh3)2, were prepared by deprotonation of the respective phenyldiazene complexes, MH(CO)2(HNNPh)(PPh3)2+ and MH(CO)(HNNPh)(PPh3)3+. The compound OsCl3(NNPh)(PPh3)2 has also been prepared. A large number of the foregoing complexes have been synthesized with selective 2H and 15N labels. Infrared and NMR spectra show MX(CO)2(NNPh)(PPh3)2 and the analogous hydrido complex to be pseudooctahedral with trans phosphine ligands, cis carbonyl ligands, and a doubly bent phenyldiazenido (NNPh-) ligand. Similarly, MH(CO)(NNPh)(PPh3)2 possesses a trigonal-bipyramidal geometry with trans phosphine ligands and an equatorial, singly bent phenyldiazoniumato (NNPh+) ligand. Isotopic substitution of the diazo ligand shows that ν(NN) is often vibrationally coupled with phenyl vibrational modes and that two or three bands sometimes shift upon 15N substitution. Vibrational coupling is also observed in the higher energy region (1850-1900 cm-1) in the compound RuCl3(NNC6D5)(PPh3)2. The wide range in the values of ν(NN), RuCl3(NNPh)(PPh3)2 (1882 cm-1), vs. RuCl-(CO)2(NNPh)(PPh3)2 (1462 cm-1), indicates that the N-N stretching frequencies are sensitive to the electronic and steric environment of the diazo ligand. The aryldiazo complexes are compared with analogous, isoelectronic nitrosyl complexes of Os and Ru.

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