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[(PtMe3(μ-I))2(μ-bis(diphenylphosphino)methane)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133892-26-9

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133892-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133892-26-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,8,9 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133892-26:
(8*1)+(7*3)+(6*3)+(5*8)+(4*9)+(3*2)+(2*2)+(1*6)=139
139 % 10 = 9
So 133892-26-9 is a valid CAS Registry Number.

133892-26-9Downstream Products

133892-26-9Relevant academic research and scientific papers

Oxidative addition of methyl iodide to a new type of binuclear platinum(II) complex: A kinetic study

Jamali, Sirous,Nabavizadeh, S. Masoud,Rashidi, Mehdi

, p. 8594 - 8601 (2005)

A new organodiplatinum(II) complex cis,cis-[Me2Pt(μ-NN)(μ- dppm)PtMe2] (1), in which NN = phthalazine and dppm = bis(diphenylphosphino)methane, is synthesized by the reaction of cis,cis-[Me2Pt(μ-SMe2)(μ-dppm)PtMe2] with 1 equiv of NN. Complex 1 has a 5dπ(Pt) → π*(imine) metal-to-ligand charge-transfer band in the visible region, which was used to easily follow the kinetics of its reaction with MeI. Meanwhile, the complex contains a robust bridging dppm ligand that holds the binuclear integrity during the reaction. A double MeI oxidative addition was observed, as shown by spectrophotometry and confirmed by a low-temperature 31P NMR study. The classical SN2 mechanism was suggested for both steps, and the involved intermediates were suggested. Consistent with the proposed mechanism, the rates of the reactions at different temperatures were slower in benzene than in acetone and large negative ΔS? values were found in each step. However, some abnormalities were observed in the related rate constants and ΔS? values, which were demonstrated to be due to the associative involvement of the polar acetone molecules in the reactions. The rates are almost 6 times slower in the second step as compared to the first step because of the electronic effects transmitted through the ligands and the steric effects.

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