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Tris(2,3,4,5-tetramethylphenyl)phosphine, also known as TMPP, is a phosphine ligand with the chemical formula C24H33P. It is a sterically hindered, electron-rich phosphine, which makes it a popular choice in homogeneous catalysis, particularly in transition metal complexes. TMPP is known for its stability, high solubility in organic solvents, and its ability to form strong bonds with metal centers. This ligand is often used in the synthesis of various metal complexes, such as those involving palladium, platinum, and nickel, which are important in applications like hydrogenation, hydroformylation, and cross-coupling reactions. The bulky tetramethylphenyl groups on the phosphorus atom provide steric protection, which can help control the selectivity and activity of the resulting catalysts. TMPP's unique properties make it a valuable tool in the field of organometallic chemistry and catalysis.

66417-52-5

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66417-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66417-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,1 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66417-52:
(7*6)+(6*6)+(5*4)+(4*1)+(3*7)+(2*5)+(1*2)=135
135 % 10 = 5
So 66417-52-5 is a valid CAS Registry Number.

66417-52-5Downstream Products

66417-52-5Relevant academic research and scientific papers

Anodic Bahavior of Crowded Triarylphosphines. ESR Study of Triarylphosphoniumyl Radicals, Ar3P.+

Culcasi, Marcel,Berchadsky, Yves,Gronchi, Gerard,Tordo, Paul

, p. 3537 - 3542 (2007/10/02)

A large number of triarylphosphines exhibiting different steric hindrance has been prepared.The pyramidalization angle α of these compounds was calculated with use of the MM2 force field and was shown to depend almost exclusively on the number of ortho substituents on the phenyl rings.In a series of isosteric (same α) phosphines, the oxidation potential correlates with the sum of the ?+ Hammett parameters of the phenyl substituents.In the absence of oxygen, anodic oxidation of all the triarylphosphines bearing two o-methyl substituents on each phenyl ring is reversible and yields very persistent phosphoniumyl radicals.These radicals are easly detected by ESR in liquid solution and were shown to retain a pyramidal geometry that is significantly flattened compared to that of the parent phosphine.

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