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Rh(CO)(As(C6H5)3)2Br is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59531-98-5

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59531-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59531-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,3 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59531-98:
(7*5)+(6*9)+(5*5)+(4*3)+(3*1)+(2*9)+(1*8)=155
155 % 10 = 5
So 59531-98-5 is a valid CAS Registry Number.

59531-98-5Upstream product

59531-98-5Downstream Products

59531-98-5Relevant academic research and scientific papers

LIGATING PROPERTIES OF THIONITROSOAMINES. III. CARBONYL COMPLEXES OF RHODIUM(I) AND RHODIUM(III) CONTAINING N-THIONITROSODIMETHYLAMINE

Tresoldi, Giuseppe,Sergi, Sergio,Schiavo, Sandra Lo,Piraino, Pasquale

, p. 369 - 376 (1987)

Me2NNS reacts with 2 to produce the complex cis-Rh(SNNMe2)(CO)2Cl (1).The latter undergoes reversible CO substitution by Me2NNS to give the complex trans-Rh(SNNMe2)2(CO)Cl (2a).Complexes 1 and 2a, in solution lose CO and Me2NNS, respectively, to give the complex trans-(μ-Cl)22 (3).Complex 1 can also be prepared by dubbling CO through a CH2Cl2 solution of Rh(SNNMe2)(diene)Cl (diene=1,5-cyclooctadiene (4a), norbornadiene (4b)) obtained by a bridge-splitting reaction of Me2NNS with 2. 1 and 2a react with EPh3 (E=P, As, Sb) to give the complexes trans-Rh(EPh3)2(CO)Cl.The complexes trans-Rh(E'Ph3)2(CO)X (X=Cl, E'=As, Sb; X=Br, NCS, E'=As) undergo reversible E'Ph3 displacement upon treatment with Me2NNS to give the complexes trans-Rh(SNNMe2)2(CO)X (X=Cl (2a), Br(2b), NCS (2c)).Oxidative additions of Br2, I2, or HgCl2 to 2a produce stable adducts, while the reaction of 2a with CH3I gives an inseparable mixture of the adduct Rh(SNNMe2)2(CO)(CH3)ClI and the acetyl derivative Rh(SNNMe2)2(CH3CO)ClI.A mixture of the acetyl derivative (μ-Cl)22 and the adduct (μ-Cl)22 is obtained by treating 1 with CH3I.The IR spectra of all the compounds are consistent with S-coordination of Me2NNS.Because of the restriced rotation around the N-N bond, the 1H NMR spectra of the new compounds exhibit two quadruplets in the range 3.5-4.3δ when 4J(HH)=0.7-0.5 Hz.When 4J(HH)0.5 Hz, the perturbing effect of quadrupolar relaxation of the 14N nucleus obscures the spin-spin coupling and two broad signals are observed in the range 3.6-4δ.

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